CN101422167A - Aromatic neomenthylamides as flavouring agents - Google Patents

Abstract

The present invention is directed to controlling pest infestation by inhibiting one or more biological functions in an invertebrate pest. The invention discloses methods and compositions for use in controlling pest infestation by feeding one or more different recombinant double stranded RNA molecules to the pest in order to achieve a reduction in pest infestation through suppression of gene expression. The invention is also directed to methods for making transgenic plants that express the double stranded RNA molecules, and to particular combinations of transgenic pesticidal agents for use in protecting plants from pest infestation.

Description

Be used for composition and method at plant control insect infestations

The application is that application number is the dividing an application for the Chinese patent application of " being used for composition and method at plant control insect infestations " that 200580019203.4 (international application no is PCT/US2005/011816), the applying date be on April 8th, 2005, denomination of invention.

Cross reference to related application

The present invention requires following U.S. Provisional Application: be filed in 60/560 of on April 9th, 2004,842, be filed in 60/565 of on April 27th, 2004,632, be filed in 60/579 of on June 11st, 2004,062, is filed in 60/603 of on August 20th, 2004,421, be filed in 60/617 of on October 11st, 2004,281 and the 60/_____ that is filed on April 7th, 2005, they every part all by reference integral body incorporate this paper into.

Invention field

Generally speaking, the genetic control that the present invention relates in plant and in animal and on animal, the pest invasion and attack are carried out.More specifically, the present invention relates to be used for modifying the method for the endogenous expression of specific pest cell or tissue coded sequence.More specifically, the present invention utilizes recombinant DNA technology, back containment or inhibition are transcribed in the expression of target code sequence in the pest cell, this is raise one or more and transcribe the two strands or small interference ribonucleic acid (RNA) molecule that come from part or all of target code sequence and realize by feeding to pest, is controlled attacking thus.Therefore, the present invention relates to suppress, to obtain control to the desirable level of pest by the sequence-specific that double-stranded RNA (dsRNA) or siRNA (siRNA) are expressed coded sequence.

That the present invention also provides is novel, through separating and highly purified nucleic acid molecules, it includes but not limited to be used for nucleotide sequence and recombinant DNA construction body transcript invention dsRNA or siRNA molecule, that non-natural exists, when being introduced into pest, the expression of source coding sequence or target code sequence in it can contain or suppress in the pest.The present invention also provides following genetically modified plants, (a) described plant contains following nucleotide sequence, the described nucleotide sequence coded recombinant DNA construction body that exists with highly purified nucleic acid molecules and non-natural through separating, be used to transcribe the dsRNA or the siRNA molecule that are used to control to the harmful biological attack of plant, and (b) show the resistance of insect infestations and/or the tolerance of raising.The present invention has also described: contain the composition of dsRNA nucleotide sequence of the present invention, it is used on the plant or on the animal or the environment topical application of animal, so that the pest invasion and attack are eliminated or reduced.

Background of invention

The environment of human survival has been full of the pest invasion and attack.Pest comprises: insect, spider, shellfish, fungi, bacterium, virus, nematode, flatworm, roundworm, pinworm, hookworm, tapeworm, trypanosoma, blood fluke, horse botfly, flea, flat lice, mite, lice etc., they are ubiquitous in the human environment, have used the invasion and attack of these pests of multiple means attempt control.The composition that is used to control small pest (for example bacterium, fungi and virus) invasion and attack has been provided as antibiotic composition, antiviral composition and antifungal composition form.(for example be used for the big pest of control, nematode, flatworm, roundworm, pinworm, heartworm, tapeworm, trypanosoma, blood fluke etc.) composition of invasion and attack typically exists as the form of Chemical composition that, they can be applied to has notified the material surface that has harmful biological attack, is perhaps absorbed by affected animal with forms such as pill, powder, tablet, ointment or capsules.The present invention relates to provides: than composition known in the art, be used to control improving one's methods of pest invasion and attack.

Commercial crops is the target of attack of insect normally.In the past in the many decades, be used for the more efficiently method and composition of controlling plant insect infestations, had some substantial progress about exploitation.Chemical insecticide is very effective for eradicating the pest invasion and attack.But, use chemical insecticide that multiple shortcoming is arranged.Chemical insecticide is nonselective.People's intended application chemical insecticide is controlled no vertebra pest harmful concerning various crop and other plant.But in default of selectivity, chemical insecticide also can apply its effect for non-target animal, and, in a period of time that chemical insecticide was used, can make the field barren usually.Chemical insecticide continues to be present in the environment, and is very slow in usually metabolism, if fully not by metabolism.They can accumulate in food chain, particularly in the food chain of high carnivore.The accumulation of these chemical insecticides causes the development of these reagent resistances and the high-end species of ladder that cause evolving, and described insecticide is had an effect as mutagen and/or carcinogen, causes irreversible harmful genetic modification usually.Therefore people need be used for controlling or eradicate the insect infestations on plant or the plant strongly to the method for environment friendliness, promptly, optionally, the environment inertia, non-lasting reservation and biodegradable, and can be the method that is used for pest resistance management system well.

The composition that comprises Bacillus thuringiensis (B.t.) bacterium can obtain by commercial sources, and it has used above 30 years as environmentally safe and acceptable insecticide.The insect effect of killing of Bt bacterium is the result of the protein of the proprietary generation of these bacteriums, described protein can not continue to be present in the environment, and, the selectivity that has height for affected target species, only by absorbed its effect that applies by the target pest, they have demonstrated the innocuousness to environment and other nontarget organism (comprising the mankind).The genetically modified plants of one or more genes that containing encodes kills insect B.t. albumen also can obtain in this area, and their significant effective are in the invasion and attack of control harmful insect.The substantive result who use to express the recombinant plant of Bt insecticidal protein is, in the area of using these type of genetically modified crops, is applied to environment and obviously reduces with the amount of the chemical insecticide of control crop field pest invasion and attack.The minimizing that chemical insecticide is used makes soil more clean, and makes from the soil flow also cleaning more of water in streams, rivers, pond and lake towards periphery.Except that these environmental benefits, the crop field of the anti-insect plant growth of transgenosis, the quantity of favourable insect has remarkable increase, and this is because the cause that the use of chemical insecticide reduces.

Reported the antisense method and composition in this area, their are believed that can pass through single stranded RNA molecule (in theory, can be in vivo with highly the positive-sense strand RNA molecular hyridization of complementation) synthetic applies its effect.Antisense technology is difficult to use in a lot of systems, and this has three main causes.At first, the antisense sequences instability of expressing in the transformant.The second, the lability of the antisense sequences of expressing in the transformant causes difficulty to host, cell type or the biosystem that this sequence is transported to away from transgenic cell thereupon.The 3rd, along with the difficulty that transporting of lability and antisense sequences runs into has also been made difficulty for following attempt, described attempt is: the recombinant cell inside at this antisense sequences of coding provides the dosage that can effectively regulate the positive sense nucleotide sequence expression of target.

The technology that is used for regulatory gene expression in cell, tissue or biology rarely has improvement, especially, lacks the technology that is used for postponing, containing or reduce by the use recombinant DNA technology development that specific gene is expressed.In addition, as the result of the Unpredictability of these means, be not used in eucaryon or prokaryotes, regulate the specific gene expression, the obtainable means of commercial sources.

Showed the inhibition of in multiple pest, specific gene being carried out double chain RNA mediate in the past.In fruit bat Drosophila melanogaster to dsRNA mediation be used for genetically controlled means in addition detection (Tabara et al., 1998, Science282:430-431).Tabara et.al. has described a kind of method, is used to transport relate to the dsRNA that produces transgenic insect (it expresses double stranded rna molecule) or the dsRNA injection of solution is expelled in the egg capsule in insect bodies or before embryonic development.Show before the researcher, feed to raise by the solution that will contain two strands or siRNA molecule and be dipped in this solution, and by injection dsRNA molecule, the gene that can obtain double chain RNA mediate in nematode is contained to nematode or with nematode.Rajagopal et al. has described the attempt of following failure: raise the solution that contains the dsRNA that is specific to target gene by feeding, or by larva being dipped in this solution, the endogenous gene of containing harmful insect Spodoptera litura larva, but, after dsRNA being expelled to the hemolymph of the 5th attitude larva with micro syringe (microapplicator), Rajagopal et al. but successfully obtained containment (J.Biol.Chem., 2002,277:46849-46851).Similarly, Mesa et al. (Us 2003/0150017) has predictably described and has been used to use the dsRNA that is transported to larva to suppress the preferred gene seat of lepidoptera larva Helicoverpaarmigera, and described transporting by having absorbed the plant that is converted into generation dsRNA realized.It is believed that it is unpractical providing composition that the dsRNA molecule maybe will contain dsRNA to be expelled in the no vertebra harmful organisms in great majority do not have the meals of vertebra pest species.It is unpractical providing the meals method of dsRNA molecule to no vertebra pest, because RNA molecule, or even stable double stranded rna molecule, at gentle alkalescence or sour environment (for example, do not have at great majority and to be found in the vertebra pest digestive tract) in also be highly unsettled, degraded by the nuclease in the environment easily.Therefore, people need be in specific no vertebra pest by containment, postpone or reduce improving one's methods that gene expression come that regulatory gene expresses, described method is for the purpose of controlling the pest invasion and attack or be used to introduce new phenotypic character.

Summary of the invention

The present invention in one embodiment, comprises and suppresses the method that target gene is expressed in the no vertebra pest.Especially, the present invention comprises to no vertebra pest (especially, Western corn rootworm (WCR, Diabrotica virgifera virgifera LeConte)) method that the expression of one or more target genes is regulated or suppressed in, described method can cause feed, growth, growth, breeding and propagate stopping, and finally causes insect death.Described method comprises: will be through stable double-stranded RNA (dsRNA) or its modified forms (for example, siRNA (siRNA) sequence) (for example partly or entirely be incorporated into no vertebra harmful insect cells in vivo or extracellular environment, midgut) in, in no vertebra harmful insect body, dsRNA or siRNA enter into cell, at least a or plurality of target expression of gene are suppressed, and, wherein, being suppressed on the no vertebra pest of one or more target genes expression applied deleterious effects.What consider especially is, method and composition of the present invention will be useful on: comprise the composition of dsRNA molecule by one or more are provided in the pest meals, the invasion and attack of restriction or the no vertebra pest of elimination in the environment of any pest host, pest symbiont or pest hobby, as long as pest digestive system pH about 4.5 to about 9.5 scope, about 5 to about 9, about 6 to about 7 and about pH7.0.

The invention discloses exemplary sequence table, wherein contain from Western corn rootworm (WCR, Diabrotica virgifera) nucleotide and amino acid sequence, shown in SEQ ID NO:1 to SEQ ID NO:143 and SEQ ID NO:169 to SEQ ID NO:174, also contain from other coleopterous insect, comprise Colorado potato bug (CPB, Leptinotarsa decemlineata) and red flour beetle (RFB, Tribolium castaneum); From lepidopterid, comprise European corn borer (ECB, Ostrinia nubilalis), black cutworm (BCW, Agrotis ipsilon), Heliothis zea (CEW, Helicoverpa zea), autumn armyworm (FAW, Spodoptera frugiperda), boll weevil (BWV, Anthonomus grandis), silkworm (Bombyx mori) and Manduca sexta, and from dipteron, comprise Drosophila melanogaster, Anopheles gambiae and Aedes aegypti sequence, shown in SEQ ID NO:144 to SEQ ID NO:159.Sequence table is comprised with the form of the CD-ROM CD papery copy with the application.

Submit to, contain sequence table information corresponding to the computer-reader form of sequence table at following sequence: the sequence of corn rootworm Unigene sequence, est sequence, corn rootworm specific probe sequence, primer sequence, amplicon sequence and coding double-stranded RNA sequence and v-ATPase and from the ribosome L19 of above-mentioned other insect directly to autoploid (SEQ IDNO:144 to SEQ ID NO:159).

The invention provides a kind of method, be used for the gene expression of the no vertebra pest of containment (for example corn rootworm or relevant species), described method comprises the steps: to provide at least a dsRNA molecule of gene containment amount in the meals of pest, described dsRNA molecule is to be transcribed by the nucleotide sequence shown in SEQ ID NO:1 to SEQ ID NO:143 in the sequence table and SEQ ID NO:169 to the SEQ ID NO:174, the mRNA sequence complementation that forms in its at least one section segment and the pest cell, and the dead or feed of observation pest is suppressed, hinder or stop.

In another aspect of this invention, described method comprises the steps: to feed to pest raises a kind of (or multiple) through stable dsRNA molecule or its modified forms, it is identical that siRNA molecule for example, its nucleotide sequence and the nucleotide sequence that is selected from the group that is made of SEQ ID NO:1 to SEQ ID NO:143 and SEQ ID NO:169 to SEQ ID NO:174 are transcribed the RNA molecule about at least 80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99 or about 100% that comes.

Therefore, in another aspect of this invention, provide the nucleotide sequence of a group shown in SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table and SEQ ID NO:169 to the SEQ ID NO:174 through separation and purifying.Nucleotide sequence shown in SEQ ID NO:1 to the SEQ ID NO:143 disclosed herein is from being separated by complementary DNA (cDNA) library of WCR insect larvae preparation and being purified in fact.Nucleotide sequence in the sequence table disclosed herein shown in SEQ ID NO:169 to the SEQ ID NO:174 separates and highly purified genomic DNA from harmful Southern corn rootworm, or the mRNA storehouse of this harmful insect, obtain by this class mRNA storehouse or based on known in nucleotide sequence disclosed herein or this area as the from the beginning synthetic cDNA nucleotide sequence of T7 phage rna polymerase promoter sequence.The invention provides through stable dsRNA or siRNA molecule, or the expression of one or more miRNA, be used for suppressing no vertebra pest, for example expression of target gene in the WCR insect.Through stable dsRNA, miRNA or siRNA molecule can comprise at least two kinds of coded sequences that at least a relatively promotor is arranged with justice or antisense orientation, wherein, the nucleotide sequence that comprises positive-sense strand and antisense strand is connected or connects by about at least five intervals to about 1,000 nucleotide (spacer) sequence, wherein, positive-sense strand is different with antisense strand length, and wherein, the nucleotide sequence shown in one of one of SEQ ID NO:1 to SEQ ID NO:143 or SEQ ID NO:169 to SEQID NO:174 shares at least 90% in two kinds of coded sequences each and the sequence table, at least 95%, at least 98% or even 100% sequence homogeny.

(NNO) nucleotide sequence that the present invention also provides non-natural to exist, it can be used to target does not have gene in the vertebra pest, is used for the containment of double chain RNA mediate, with the inhibition to target gene that obtains to want.Nucleotide sequence shown in SEQ ID NO:1 to SEQ ID NO:143 or SEQID NO:169 to the SEQ ID NO:174 any is used to make up this type of NNO nucleotide sequence.

The present invention also provides code book to invent the reorganization dNA construct of the dsRNA molecule that is comprised, and is used to introduce host cell.The recombinant DNA construction body comprises the nucleotide sequence that is transcribed into RNA by host cell.The RNA that transcribes forms at least a dsRNA molecule, makes that a chain of dsRNA molecule is coded by the part of the nucleotide sequence identical with the nucleotide sequence about at least 80% to about 100% that is selected from the group that is made of SEQ ID NO:1 to SEQ ID NO:143 and SEQ ID NO:169 to SEQ ID NO:174.The recombinant DNA construction physical efficiency produces the dsRNA molecule in host cell, can suppress endogenous gene or target gene or derivatives thereof or its complementary series in host cell, or not have vertebra pest picked-up expression in the pest cell after transformed host cells.Nucleotide sequence of the present invention be in the host cell can operated promoter sequence control under, and expressed the RNA sequence that forms the dsRNA molecule in the host cell to be created in.At host cell or do not have in the vertebra pest dsRNA molecule is further processed, form the siRNA molecule.

The present invention also provides the recombinant DNA sequence that is used for Plant Transformation, and it is built as the nucleotide sequence that contains at least a non-natural existence that can be converted into the single stranded RNA molecule.Under situation about providing in the meals of no vertebra pest, the single stranded RNA molecule forms double stranded rna molecule by intermolecular hybridization in vivo, suppresses the expression of at least a target gene in the no vertebra pest cell.The nucleotide sequence that non-natural exists is operably connected with at least a promoter sequence, described promoter sequence plays a role in transgenic plant cells, and the nucleotide sequence that the non-natural that is operably connected is existed is transcribed into one or more RNA sequence.The RNA sequence self is assembled into double stranded rna molecule, is provided in the meals of the no vertebra pest of taking food on genetically modified plants.The supply of the dsRNA molecule in the meals of pest has obtained the inhibition of wanting that one or more target genes in the pest are expressed.

The present invention also provides following recombinant host cell, described host cell has at least a recombinant DNA sequence in its genome, described dna sequence dna can be transcribed in host cell, to produce at least a dsRNA molecule, when being digested by no vertebra pest, described dsRNA molecule plays a role, to suppress the expression of target gene in the pest.The dsRNA molecule is coded by the part of following nucleotide sequence, described nucleotide sequence show with sequence table in about at least 80 to about 100% homogeny of the nucleotide sequence shown in SEQ ID NO:1 to SEQ ID NO:143 or SEQ ID:169 to the SEQ ID NO:174.Be used for making up target WCR gene and be shown in sequence table SEQ ID NO:1 to SEQ ID NO:143 and SEQID:169 to SEQ ID NO:174 with the Exemplary core nucleotide sequence of the dsRNA reagent that suppresses.

The present invention also provides the recombinant DNA construction that is used for Plant Transformation body, described construct is made of the sequence that at least two kinds of different non-naturals exist, when expressing in vivo as the RNA sequence and providing in the meals of no vertebra pest, described sequence can suppress at least two kinds of different target expression of gene in the no vertebra pest cell.The sequence of first kind of non-natural existence is converted into RNA, and it forms at least a first kind of dsRNA molecule.The part of first kind of dsRNA molecule is coded by the part of the sequence that first kind of non-natural exists, its show with sequence table in about at least 80 to about 100% the homogeny of nucleotide sequence, its derivative or its complementary series of the nucleotide sequence shown in SEQ ID NO:1 to SEQ ID NO:143 or SEQ ID:169 to the SEQ ID NO:174, first kind of target gene.The sequence of second kind of non-natural existence is converted into RNA, and it forms second kind of dsRNA molecule.The part of second kind of dsRNA molecule is coded by the part of the sequence that second kind of non-natural exists, and it shows and be selected from about at least 80 to about 100% homogeny of nucleotide sequence, its derivative or its complementary series of the nucleotide sequence shown in SEQ ID NO:1 to SEQ ID NO:143 in the sequence table or SEQ ID:169 to the SEQ ID NO:174 and second kind of target gene.The sequence of two kinds of non-natural existence operationally is positioned under the control of at least a promoter sequence.Promoter sequence performance function is to express first kind and second kind of dsRNA molecule in transgenic plant cells.Being provides the dsRNA molecule of pest inhibition concentration in the meals of the no vertebra pest of taking food on the genetically modified plants, and pest can obtain the inhibition of wanting that target gene in the pest is expressed to the picked-up of plant cell.

The present invention also provides through the plant transformed cell, and it has at least a of the recombinant DNA sequence that is used for Plant Transformation mentioned above in its genome.Produce genetically modified plants through the plant transformed cell, genetically modified plants are made progeny plants, seed and plant product, they each all comprise recombinant DNA.

Method and composition of the present invention can be applicable to any unifacial leaf and dicotyledon, this depends on the no vertebra pest control of wanting, perhaps, it can be applied on the invertebrate by pharmaceutically acceptable preparation, so that there is not the reduction that certain level takes place the invasion and attack of vertebra pest.Especially, plant includes but not limited to: alfalfa, dill (aneth), apple, apricot, artichoke, rocket salad, asparagus, avocado, banana, barley, beans, beet (beet), blackberry, blueberry, blueberry, cabbage, brussels sprouts, cabbage, leaf mustard, muskmelon, carrot, cassava, cauliflower, celery, cherry, coriander, oranges and tangerines, the little oranges and tangerines of Ke Laimenshi, coffee, corn, cotton, cucumber, pesudotsuga taxifolia, eggplant, hare's-lettuce, wide leaf lettuce, eucalyptus, fennel, fig, cucurbit, grape, shaddock, Hami melon, yam bean, Chinese grooseberry, lettuce, leek, lemon, bitter orange, torch pine, mango, melon, mushroom, nut, oat, okra, onion, tangerine, decorate and use plant, pawpaw, parsley, pea, peach, peanut, pears, pepper, persimmon, pine tree, pineapple, plantain, Lee, pomegranate, white poplar, potato, pumpkin (pumpkin), Wen Bai, pine, witloof, radish, raspberry, paddy rice, naked barley, Chinese sorghum, the south pine, soybean, spinach, pumpkin (squash), strawberry, beet (sugarbeet), sugarcane, sunflower, Ipomoea batatas, storax, mandarin orange, tea, tobacco, tomato, turf, vining plant, watermelon, wheat, Chinese yam and Xiao Hu's melon plant.

The present invention also provides a kind of pest control reagent, wherein comprises from nucleotide sequence of the present invention and transcribes next dsRNA molecule.The nucleotide sequence shown in SEQ IDNO:1 to SEQ ID NO:143 or SEQ ID:169 to the SEQ ID NO:174 is shared about 80 to about 100% homogeny in described nucleotide sequence and the sequence table.In one form, pest control reagent comprises the dsRNA molecule.In another form, pest control reagent comprises the siRNA molecule.In another form, pest control reagent comprises the recombinant DNA sequence of the following mRNA molecule of encoding, and described mRNA molecular energy is formed for dsRNA or the siRNA molecule of introduced plant and microorganism.In a kind of form also, pest control reagent is microorganism, and it contains the recombinant DNA sequence of the following mRNA molecule of encode, described mRNA molecular energy formation dsRNA or siRNA molecule.Pest control reagent is insect or nematoda pest control reagent preferably.

People need be harmful to BIOLOGICAL CONTROL reagent and play a role, to reduce or eliminate the invasion and attack of corn rootworm, but also consider, method and composition shown in this paper can be used to obtain the correlated series from other pest, and utilizes these derivatives to control the invasion and attack of other (multiple) pest.Consider that also the insect pest can be selected from same genus, the mutually equal or order under the corn rootworm.In addition, the present inventor also considers, can use the present invention, is applied to control from Bugdom with from nematode, fungal pathogens, virus, bacterium and any other any species to the harmful invertebral living creature of plant.

The present invention also provides the combination of the method and composition that is used to control no vertebra pest invasion and attack.A kind of means provide and have been used for protective plant and keep out dsRNA method and composition insect infestations, as herein described, and one or more insecticides, and described insecticide shows the character of the different in kind that is shown with the dsRNA method and composition.For example, when in the meals of insect pest, providing Bt albumen, just shown the binding mode of controlling the insect pest with dramatic different being used to of the binding mode of method and composition of the present invention.Be formulated as the composition of topical application, or the composition that dsRNA method and composition and Bt method and composition are combined that uses transgenic method to obtain, can produce synergistic effect, this be in the field of control insect infestations before the unknown.The genetically modified plants that produce one or more dsRNA or siRNA molecule (can suppress in the target pest some necessary biological functions) provide astonishing synergistic effect with one or more poisonous concerning the target pest B.t. insecticidal proteins.A kind of synergistic effect is that the required expression of (multiple) dsRNA or (multiple) Bt albumen reduces.When being grouped together, every kind of pest controlling agent all only needs lower effective dose.It is believed that, the Bt insecticidal protein has produced and has entered the hole, dsRNA or siRNA molecule can more effectively penetrate into space away from insect gut by the described hole that enters, perhaps more effectively penetrate near the cell of wound of Bt albumen manufacturing, only need the Bt of less amount or the insect result extremely that dsRNA just can obtain to want thus, inhibition or the containment perhaps wanted to target pest target organism function.

The present inventor has described multinomial invention in this article, comprising the method that is used to control no vertebra pest invasion and attack, described method is by providing following reagent to carry out in the meals of no vertebra pest, the ribonucleic acid that described pack plays a role when being contained in and being absorbed by pest, perhaps constitute, to suppress the expression of pest cell internal object nucleotide sequence by described ribonucleic acid.The ribonucleic acid that in meals, provides by be the target nucleotide sequence or constitute with the ribonucleotide acid sequence of target nucleotide sequence complementation.The ribonucleotide acid sequence is to be transcribed by following continuous dna sequence dna, it is about at least 19 long to about 5000 nucleotide that described dna sequence dna has, and it is selected from the group that is made of SEQ ID NO:1 to SEQ ID NO:143, SEQ ID:169 to SEQ ID NO:174 and complementary series thereof.Described method provides the structure to following nucleotide sequence, and described nucleotide sequence can be used for the expressed rna molecule, and described RNA molecule is absorbed by pest in offering the meals of pest.Meals can be artificial meals, it was carried out preparation to reach the specific nutrition requirement that keeps pest on these type of meals, described meals can be supplemented with the pest controlled quentity controlled variable, the RNA that from independent expression system, is purified into, meals additional is used for following purpose: the pest controlled quentity controlled variable of determining the RNA composition, or determine---when the meals that the pest picked-up is replenished, can combine specifically with one or more target sequences in the pest and part hybridization, whether the specific RNA of one or more structures is useful on obtains some gene containment activity.Meals can also be the recombinant cells that transformed with dna sequence dna, and described DNA contains that at reagent, RNA or gene the expression of agent makes up.Pest absorb one or more this type of when the cell transformed, can observe the genotype or the phenotype result that want, this shows, this reagent has and suppresses the function that pest cell internal object nucleotide sequence is expressed.

No vertebra pest is insect, spider, nematode, flatworm, capsule worm, fungi pest or gene containment technology other any no vertebra pest applicatory preferably.More preferably, no vertebra pest is a no vertebra pest under a cloud especially aspect the animal or plant invasion and attack.More particularly, no vertebra pest is insect or the nematode or the fungi pest on preference invasion and attack crop plant, ornament and/or meadow.

It is about 19 long to about 5000 nucleotide to select for use the dna sequence dna of expressing gene of the present invention containment agent to be preferably, and the justice or the antisense strand of the target sequence that it exists to small part and one or more specific objective pest species DNA are highly identical on sequence.Phrase " to small part " is intended to represent following notion: select for use expressing gene to contain that the dna sequence dna of agent can be by the wall scroll sequence construct that obtains from one or more target pests, it can be used to express following RNA, described RNA can be in to one or more target pests the containment of individual gene or gene family retransmit the effect of waving; Perhaps can make up as chimeric dna sequence dna from multiple dna sequence dna.Described multiple dna sequence dna can all obtain from single one or more nucleotide sequences of planting in the pest by each bar, perhaps can obtain from one or more nucleotide sequences of multiple different pests.Especially, the sequence of selecting should show and about 80 to about 100% nucleotide sequence homogeny from the nucleotide sequence of pest species DNA.The DNA of pest species can identify by following method: isolate DNA from the pest species, perhaps by the RNA in the pest species is identified, oppositely change the RNA sequence into DNA.Come out sequence from the DNA of corn rootworm pest species of example is SEQ ID NO:1 to SEQ ID NO:143, SEQ ID:169 to SEQ ID NO:174 and a complementary series thereof that illustrate herein, in the sequence table.

Select for use the dna sequence dna of expressing gene containment property RNA molecule can be included in the polynucleotide compositions, described composition uses in plant cell.Especially, dna sequence dna can be comprised into being used for the genomic carrier of transformed plant cells, and can be comprised into expression cassette, described expression cassette contains at least a plant function promotor, and described promotor operationally links to each other with any expression control element of the dna sequence dna of selecting for use and other (wanting to be used for obtaining the expression of interior time of suitable cell or plant space level).Polynucleotide compositions is incorporated in the genome of plant cell transformant is provided,, and be regenerated as the transgenosis recombinant plant if suitable selection approach is comprised with polynucleotide compositions that it can be selected so.Genetically modified plants, incident can be provided in the meals of one or more pests, to obtain the control to the pest invasion and attack.Genetically modified plants can produce progeny plants, plant cell and seed, they each all contain polynucleotide compositions.

The invention provides a kind of protective plant and keep out the method for insect infestations; described method is by providing in the following plant cell one or more to realize to the insect pest; every kind in described cell is the RNA molecule of expressing gene containment property all; described RNA molecule is from following dna sequence dna, and described dna sequence dna is selected from the group that sequence constituted of being given an example by this paper.Contain the picked-up of the plant cell of property RNA, pest or insect-controlling agent to containing gene, caused inhibition one or more biological functions in pest or the insect.

The invention provides a kind of composition, wherein contain two or more different insecticides, wherein every kind all poisonous to same pest or insect species.As described herein, a kind of in these insecticides can be the RNA molecule that is useful on the necessary biological function of containment in one or more cells of pest.Second kind of insecticide can be comprised with first kind.Second kind of insecticide can be to be different from second kind of gene containment property RNA of first kind, and perhaps second kind of insecticide can be selected from the group that following material constitutes: potato tubers storage protein patatin, Bacillus thuringiensis insecticidal protein, Xenorhabdus insecticidal protein, Photorhabdus insecticidal protein, Bacillus laterosporous insecticidal protein, Bacillussphearicus insecticidal protein and lignin.Bacillus thuringiensis insecticidal protein can be any kind of in a large amount of insecticidal proteins, and described albumen includes but not limited to: the insect chimera extremely of any kind of of Cry1, Cry3, TIC851, CryET70, Cry22, double base insecticidal protein CryET33 and CryET34, double base insecticidal protein CryET80 and CryET76, double base insecticidal protein TIC100 and TIC101, double base insecticidal protein PS149B1, VIP insecticidal protein, TIC900 or associated protein, TIC901, TIC1201, TIC407, TIC417 and aforementioned insecticidal protein.

At containing by target, at the function in the pest cell or as the physiology of pest or the function of metabolism aspect (can be produced by the expression of gene of target) at containment by the albumen of gene codified necessity of target, the expectation function of described albumen is selected from the group that is made of following function: muscle forms, the formation of juvenile hormone, the regulation and control of juvenile hormone, ion regulation and control and transhipment, synthesizing of digestibility enzyme, the maintenance of cell membrane gesture, amino acid bio is synthetic, amino acid degradation, sperm forms, pheromones synthetic, pheromones sensing, the formation of it linear protein (antennae), wing forms, the formation of leg, grow and differentiation the formation of ovum, the larva maturation, the formation of digestibility enzyme, synthesizing of hemolymph, the maintenance of hemolymph, neurotransmission, cell division, energy metabolism, breathe and apoptosis.Preferably, select for use the dna sequence dna that makes up the containment construct from shown in the sequence table, be used to contain that the nucleotide sequence of corn rootworm gene obtains.We expect, the method that is used for controlling no vertebra pest invasion and attack will comprise: the meals no vertebra pest provide reagent, for example, first kind of ribonucleotide acid sequence from first kind of dna sequence dna expression, it brings into play function when being absorbed by pest, to suppress the biological function in the described pest, expect that also first kind of dna sequence dna shows the nucleotide sequence homogeny with the coded sequence about 85 to about 100% that obtains from described pest.First kind of ribonucleotide acid sequence can with second kind of ribonucleotide sequence hybridization, described second kind of ribonucleotide acid sequence and first kind of ribonucleotide acid sequence are complementary or complementary in fact, second kind of ribonucleotide acid sequence is that second kind of dna sequence dna is expressed, second kind of dna sequence dna is corresponding to the coded sequence that obtains from no vertebra pest, and it is selected from this paper at the sequence shown in the sequence table or its complement.Preferably, first kind with second kind of dna sequence dna comprise with the sequence shown in the sequence table in one or more identical continuous sequences, described continuous sequence has about 14 to about 25 or more continuous nucleotides.

When the insecticide that contains pest gene containment amount (for example, when meals one or more RNA molecules that produced by the expression of one or more sequences shown in this paper sequence table) are provided for following no vertebra pest, the present invention brings into play optimal function, and described pest shows about 4.5 to about 9.5, about 5.0 to about 9.0, about 5.5 to about 8.5, about 6.0 to about 8.0, about 6.5 to about 7.0 or about 7.0 digestive system pH.Alternatively, function is provided when providing in the meals at one or more pests that comprise above-mentioned digestive tract pH any kind of in method as herein described, nucleic acid, ribonucleic acid, ribonucleotide acid sequence, composition, plant, plant cell, progeny plants, seed, insect-controlling agent, pest controlling agent, the expression cassette.

Meals of the present invention can be any enough pest meals, it includes but not limited to, artificial meals or prescription, plant cell, the various plants cell, plant tissue, the root of plant, plant seed and the plant that comes from the plant seed growth, wherein, described meals comprise the pest amount of suppression, RNA molecule by following dna molecule encode, described dna molecular is or comes down to one or more and be selected from the nucleotide sequence shown in the sequence table, or be selected from the nucleotide sequence that obtains from specific no vertebra pest species continuously about at least 19 to about 5000 nucleotide, perhaps complementary or complementary in fact with it.

(include but not limited to commercially important product and/or composition on the agricultural, animal feed, agricultural product and corn product and by product, corn product and by product are to be used as to be used for the human food that consumes, perhaps be used to be intended to be used for human composition that consumes and agricultural product, it includes but not limited to, corn flour, corn flour, corn syrup, corn oil, corn starch, puffed rice, corn-dodger, contain the cereal of corn and corn by product etc.) be intended to fall into scope of the present invention, if these products and composition contain detectable amount, shown in this paper, the words of nucleotide sequence that contain any transgenic event of this type of nucleotide sequence as diagnosis.These products are useful, at least because they may obtain from crop, and can produce, contain still less big Tanaka's breeding of insecticide and organic phosphine, this is that they comprise that nucleotide into of the present invention is used for controlling the result of no vertebra pest in the invasion and attack of plant.This agricultural products and agricultural product goods are to produce from the seed of being produced by genetically modified plants, wherein, described genetically modified plants are expressed following RNA, and described RNA is from one or more continuous nucleotides of the present invention, or nucleotide of one or more no vertebra pests and complement thereof.This agricultural products and agricultural product goods also can be useful on the no vertebra pest of this agricultural products of control and agricultural product goods, for example, chain of command powder weevil, because have the RNA that can contain the pest gene in agricultural product or agricultural product goods, described RNA is that gene order shown in the present is expressed.

The present invention also provides computer-readable medium, record nucleotide sequence shown in SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table or SEQ ID NO:169 to the SEQ IDNO:174 or in its complement one or more thereon, being used for a large amount of computer baseds uses, include but not limited to, DNA homogeny and similarity searching, protein homogeny and similarity searching, transcribe comparison and artificial hybridization analysis between situation signature analysis, the genome.

Detailed Description Of The Invention

Hereinafter be detailed description of the present invention, it is provided to assist those skilled in the art to put into practice the present invention.Those of ordinary skills can not leave and make improvement under the situation of aim of the present invention or scope and change in embodiment as herein described.

The inventor finds in this article, opposite with the instruction of this area, the composition that will contain double stranded rna molecule (being made of the sequence of finding) in one or more nucleotide sequences of being expressed of no vertebra species is fed and to be raised to the no vertebra species that therefrom obtain described nucleotide sequence, has caused the inhibition to one or more biological functions in the no vertebra species.Especially, the inventor finds, will be fed respectively by the double stranded rna molecule that corn rootworm RNA sequence constitutes and raise to corn rootworm, has caused absorbing the death of the corn rootworm of this based composition, perhaps grows and differentiation is suppressed.

The inventor to the nucleotide sequence of thousands of kinds of cDNA sequences obtaining from every kind of no vertebra pest species in addition evaluation.Inferred out by the amino acid sequence that the cDNA sequence is coded, and compared with all known amino acid sequences.In the cDNA sequence much be expected to be the coding following albumen, described albumen has some annotation information relevant with them.With specific nucleotide sequence with and the relevant annotation information of coded protein sequence based on autoploidy and similitude in amino acid sequence of inferring by the translation of cDNA sequence as herein described and the obtainable database of this area public between the known amino acid sequence.At all known amino acid sequences, amino acid sequence of inferring shown in this article has been carried out BLAST, based on comparison result, every kind of amino acid sequence of inferring has been assigned possible function.Encoding, known in the art very the cDNA sequence of important protein or protein part (amino acid sequence that for example, relates to multiple metabolism or catalysis biochemical route, cell division, breeding, energy metabolism, digestion, nervous function etc.) is selected concerning existence is used for preparing the double stranded rna molecule that provides in the meals of no vertebra pest.As described herein, the picked-up of target pest contains the composition of one or more dsRNA (its at least one section segment is corresponding at least one section highly identical segment of the RNA that produces in the target pest cell), causes death, hypoevolutism or other inhibition situation of target pest.These results show that from the nucleotide sequence that no vertebra pest obtains, DNA or RNA can be used to make up the reorganization pest host or the symbiont of pest invasion and attack target.Pest host or symbiont can be converted into and contain from the nucleotide sequence that no vertebra pest obtains one or more.Transform nucleotide sequence coded one or more RNA of pest host or symbiont, described RNA forms dsRNA in by cell in host transformed or the symbiont or biofluid, make thus: if/take food on transformed host or symbiont when being harmful to biology, dsRNA can be attained in the meals of pest, this will cause the containment to one or more gene expressions in the pest cell, finally cause death, hypoevolutism or other inhibition situation of pest.

Generally speaking, the present invention relates to genetic control to no vertebra pest invasion and attack in the host living beings.More specifically, the present invention includes the method that the pest controlling agent is transported to no vertebra pest.This type of pest controlling agent causes directly or indirectly that pest keeps himself, the ability of growth or invasion and attack target host or symbiont is impaired.The invention provides in the pest meals method of utilizing through stable dsRNA, this is as the means of target gene in the containment pest, obtains thus in the host of pest target or the symbiont or the control of wanting of pest invasion and attack on every side.Use the stable dsRNA or the siRNA molecule of process of reorganization, can make genetically modified plants.

For finishing aforementioned content, the invention provides a kind of method, be used for suppressing no vertebra pest (especially, Western corn rootworm (WCR) or other coleopterous insect species) in the expression of target gene, what cause taking food, grow, grow, breed, propagate stops, and finally may cause the death of pest.Described method comprises: will partly or entirely be incorporated in the alimentation composition that pest relies on as food source through the form (for example siRNA (siRNA) molecule) of modifying through stable double-stranded RNA (dsRNA) nucleic acid molecule or its, and to make this alimentation composition take food for pest be obtainable.Picked-up to the composition that contains two strands or siRNA molecule causes the absorption of pest cell to described molecule, thereby suppresses the expression of at least a target gene in the pest cell.Inhibition to target gene has caused injurious effects to pest.DsRNA molecule or siRNA are made of the shown nucleotide sequence of any sequence among SEQ ID NO:1 to SEQ ID NO:143 and SEQ ID NO:169 to the SEQ ID NO:174, and its inhibition causes for the g and D of pest or other biological function very important protein or nucleotide agent to be reduced or to remove.The nucleotide sequence of selecting for use show with sequence table in about 80% to about at least 100% the sequence homogeny of one of the nucleotide sequence shown in SEQ ID NO:1 to SEQ ID NO:143 and SEQ ID NO:169 to the SEQID NO:174 or its complementary series.This type of inhibition is specific, transcribes that the sequence of coming selects because be selected from inhibition dsRNA or siRNA from the nucleotide sequence of a target gene part.Described method is effective in the expression that suppresses at least a target gene, can be used to suppress the target gene of a lot of other types in the pest.

The present invention also provides multi-form pest controlling agent, the minimizing of the pest invasion and attack that are used to obtain to want.In one form, the pest controlling agent comprises the dsRNA molecule.In another form, the pest controlling agent comprises the siRNA molecule.In another form, the pest controlling agent comprises the recombinant DNA construction body, and it is biology and plant that described construct can be used for stable conversion, makes through microorganism transformed or plant can encode dsRNA or siRNA molecule.In another form, the pest controlling agent is a microorganism, wherein contains the recombinant DNA construction body of coding dsRNA or siRNA molecule.

From the cDNA library and/or genomic library information provide through separation and the nucleotide sequence of purifying right.Nucleotide sequence is to obtaining from any preferred no vertebra pest, and it is used as hot amplimer, to produce dsRNA of the present invention or siRNA molecule.

The invention provides the recombinant DNA construction body, be used to obtain the specific host of pest target or the stable conversion of symbiont.Through host that conversion, the pest target or symbiont express have effective desinsection level, from the preferred dsRNA or the siRNA molecule of recombinant DNA construction body, and in the meals of pest, provide described molecule.

As through conversion, the host of pest target organism or the example of symbiont, the present invention also provides through the plant transformed cell and through plant transformed and their offspring.Express one or more dsRNA of the present invention or siRNA sequence through the plant transformed cell with through plant transformed, described sequence is from one or more dna sequence dnas or its complementary series shown in SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table and SEQ ID NO:169 to the SEQ ID NO:174.

Vocabulary used herein " gene containment " is when using at the same time, is used to refer to: be used to reduce any known method of the protein level of generation, it is the result that genetic transcription becomes mRNA and mRNA translation subsequently that albumen produces.The gene containment also is used to refer to the reduction from the protein expression of gene or coded sequence, comprises the posttranscriptional gene containment and transcribes containment.Posttranscriptional gene containment is that all or part of of transcribing the mRNA that comes from the gene of containment target or coded sequence mediates with autoploidy between the corresponding double-stranded RNA that is used to contain, and it refers to the reduction that maybe can measure on the obtainable quality entity that is used for the mRNA that combines with ribosome in cell.The RNA that process is transcribed can be just direction, brings into play so-called containment effect altogether, can be antisense orientation perhaps, brings into play so-called antisense containment effect, perhaps produces dsRNA with two kinds of directions, brings into play so-called RNA interference effect (RNAi).Transcribing containment is that the existence of dsRNA mediates in the cell, and described dsRNA is gene containment agent, and it shows the height sequence homogeny with promoter DNA sequence or its complementary series, and performance is called as that promotor is counter to be contained.Gene containment can play a role at the natural plant gene relevant with proterties, for example, to plant provide have the reduction level, by the natural gene encoded protein, perhaps have the affected metabolite of increase or reduction level.The gene containment also can play a role to the target gene in the harmful biology of plant at following, described pest can absorb or contact the vegetable material that contains gene containment agent, and described gene containment agent is specifically designed the expression that can suppress or contain one or more homologous sequences in the pest cell or complementary series.

U.S. Patent number 5,107, open in 065,5,759,829,5,283,184 and 5,231,020: antisense or the directed RNA of justice carry out the posttranscriptional gene containment, with the gene expression in the regulation and control plant cell.DsRNA is used for containing that the purposes of plant gene is disclosed WO99/53050, WO 99/49029, U.S. Patent Application Publication No. 2003/0175965 and 2003/0061626, Application No. 10/465,800 and U.S. Patent number 6,506,559 and 6, in 326,193.

The method for optimizing that in plant, carries out posttranscriptional gene containment use justice directed and the antisense orientation, through the stable next RNA that transcribes, for example, as hair fastener and loop-stem structure.The preferred DNA construct that is used to carry out the posttranscriptional gene containment be following like this, wherein, first section fragment encoding shows the RNA of antisense orientation, its show and target gene segment to be contained between the height homogeny, described first section segment links to each other with second section segment, and second section fragment encoding shows with first section segment has highly complementary RNA.This type of construct is estimated to form loop-stem structure (this forms with second section segment hybridization by first section segment) and ring structure (seeing WO94/01550, WO98/05770, US 2002/0048814 and US 2003/0018993) from the nucleotide sequence that is connected both section segments.

Term used herein " nucleic acid " refers to from 5 ' to 3 ' the terminal DNA (deoxyribonucleic acid) of reading or the list or the double-chain polymer of ribonucleic acid base.Alternatively, " nucleic acid " also can contain exist or the reformed base of non-natural, and its permission can not reduce the polypeptide expression of this nucleic acid coding by the correct reading of polymerase.Term " nucleotide sequence " or " nucleotide sequence " refer to exist or be present in as independent strand the justice and the antisense strand of the nucleic acid in the disome.Term " ribonucleic acid " (RNA) comprises RNAi (inhibitory RNA), dsRNA (double-stranded RNA), siRNA (siRNA), mRNA (mRNA), miRNA (Microrna), tRNA (transfer RNA, quilt or do not added electric charge by corresponding acylated amino) and cRNA (complementary RNA), and term " DNA (deoxyribonucleic acid) " (DNA) comprises cDNA and genomic DNA and DNA RNA hybrid.Vocabulary " nucleic acid fragment ", " nucleic acid sequence fragment " or more common " segment " will be interpreted as by those skilled in the art: it comprises the nucleotide sequence of genome sequence, rRNA sequence, transfer RNA sequence, mRNA sequence, operon sequence and littler engineered mistake, and described sequence is expressed maybe can be transformed into marking protein, polypeptide or peptide.

Term used herein " pest " refers to insect, spider, shellfish, fungi, bacterium, virus, nematode, flatworm, roundworm, pinworm, hookworm, tapeworm, trypanosoma, blood fluke, horse botfly, flea, flat lice, mite, lice etc., they are that natural world is ubiquitous, can absorb or contact one or more (is converted into and can expresses double-stranded gene containment agent by pest host or symbiont, or be coated with described containment agent) cell, tissue or the fluid that produce, perhaps can absorb the vegetable material that contains gene containment agent." pest resistance " used herein is the feature of genetically modified plants, transgenic animal, transformed host or transgenosis symbiont, make described plant, animal, host or symbiont have resistance for the attack of pest, described attack typically can cause damage or loses described plant, animal, host or symbiont.This type of pest resistance may produce from natural sudden change, perhaps more typically, produces from the adding of giving the recombinant DNA of pest resistance.For the render transgenic plant has insect-resistant, recombinant DNA can be for example, coding insect lethal or insect repressible protein, for example (for example from the delta endotoxin of B.thuringiensis bacterium, can obtain to use in the kind in the commerce of cotton and corn), perhaps can be transcribed into the RNA molecule, in the tissue of recombinant plant or fluid, form the dsRNA molecule.The dsRNA molecular moiety comprises: with the identical RNA segment of corresponding RNA segment of dna sequence encoding in the harmful insect that preference is taken food on recombinant plant.Expression of gene is contained by dsRNA in the target harmful insect, causes plant to have insect-resistant to the containment of gene expression in the target harmful insect.Fire et al. (U.S. Patent number 6,506,599) has described the inhibition to the pest invasion and attack prevailingly, only provides details at the some middle nucleotide sequence that has the suppressor function in nematode kind Caenorhabditis elegans.Similarly, Plaetinck et al. (US2003/0061626) has described dsRNA and has been used for purposes in multiple nematode pest kind suppressor function.Mesa et al. (US 2003/0150017) has described: use the dsRNA sequence to remove transformed host cell, to express the corresponding dsRNA sequence identical with target sequence height in the special pathogen, and described especially: make up recombinant plant, it expresses these dsRNA sequences (being used for by the multiple biological uptake harmful to plant), assistance is to the negative accent of gene in the pest genome, and the raising plant is to the resistance of pest invasion and attack.

The invention provides the method that the gene expression of one or more target genes in the target pest is suppressed through stable dsRNA of using.The present invention is particularly useful in the adjusting eukaryotic gene expression, particularly regulate the expression of gene that exists in the insect, described insect shows about 4.5 to about 9.5, more preferably about 5.0 to about 8.0, further more preferably about 6.5 to about 7.5 digestive system pH.Digestive system with the pH level outside these scopes must not be the preferred candidate person of following method to the harmful biology of plant, method described method double chain RNA mediate, that be used for the gene containment is wherein used the method for transporting that needs the preferred dsRNA molecule of picked-up.Regulating action is applicable to the several genes of expressing in pest, for example, be responsible for the endogenous gene of conversion in endocellular metabolism or the cell, comprises other gene of the polypeptide that household's gene, transcription factor and Codocyte intracellular metabolite relate to.

Term used herein " expression " refers to, from the justice of nucleic acid acquisition disclosed by the invention or transcribing and stable accumulation of antisense RNA.Expression can also be represented the translation of mRNA to polypeptide or protein.Term used herein " justice " RNA refer to corresponding to the rna transcription of following sequence or segment this, when being produced by the target pest, described sequence or segment are existing by the form that target pest cell is translated into the mRNA of protein.Term used herein " antisense RNA " refer to target pest cell in all or part of complementary RNA of the normal mRNA that produces.The complementation of antisense RNA can be any part at the specific gene transcript, that is, and and 5 ' non-coding sequence, 3 ' non-translated sequence, intron or coded sequence.Term used herein " rna transcription this " refers to, the product that is obtained by transcribing of RNA polymerase catalysis that dna sequence dna is carried out.When rna transcription originally was the perfect complementary copy of dna sequence dna, it was called as the one-level transcript, and perhaps it can be that the one-level transcript is transcribed the RNA that back processing obtains, and it is called as mature rna.

Phrase used herein " to the inhibition of gene expression " or " suppressing the expression of target gene in the insect cell " refer to that there be not (or observable reduction) in the albumen of target gene and/or mRNA product level.Specificity refers to: suppress target gene and other gene of pair cell does not have effect and the ability that any gene in the cell that produces the dsRNA molecule not have influence.May cause new phenotypic character in the harmful insect to the inhibition of the gene expression of target gene in the harmful insect.

Under the situation that does not limit the scope of the invention, the present invention provides a kind of method in one aspect, is used for: use the invasion and attack of controlling the target pest through stable dsRNA strategy.Described method relates to: make through stable dsRNA molecule, as a kind of insect-controlling agent, induce the gene silencing in the harmful insect.Insect-controlling agent of the present invention can be induced the PTGS incident of target gene in the insect directly or indirectly.Negatively transfer the growth that can prevent or postpone at least insect, growth, breeding and to what target gene was expressed to host's propagation.Phrase used herein " is made through stable dsRNA molecule " and referred to: the recombinant DNA technology that is easy to obtain in use this area (for example, see Sambrook, et al, In:Molecular Cloning, A Laboratory Manual, 2nd Edition, Cold Spring Harbor Press, ColdSpring Harbor, New York, 1989), make up the method for transcribing through the dna nucleotide sequence of stable dsRNA.Detailed construction method of the present invention is disclosed in this specification hereinafter.Term used herein " silence " refers to, effectively " bear and transfer " what the target nucleotide sequence was expressed, and the ability of therefore this sequence generation effect in insect cell disappears.

A part of the present invention provides a kind of movement system, is used for insect-controlling agent is transported to insect, and this is to realize by they being exposed to the meals that contain insect-controlling agent of the present invention.According to one of embodiment, can be comprised into insect meals through stable dsRNA or siRNA molecule, perhaps can be placed to the top of the meals of insect consumption.

A part of the present invention also provides and has been used for insect-controlling agent is transported to insect, this be by: they are exposed to microorganism or the host of containing insect-controlling agent of the present invention, for example, plant is realized by ingested microorganisms or host cell or cellular content.In another kind of embodiment, the present invention relates to: make transgenic plant cells or plant, wherein contain the recombinant DNA construction body that to transcribe the stable dsRNA molecule of process of the present invention.Phrase used herein " is made transgenic plant cells or plant " and is referred to following method, comprise and use the recombinant DNA technology that is easy to obtain in this area (for example, see Sambrook, et al.), structure can be transcribed the plant conversion carrier of the stable dsRNA molecule of process of the present invention, transformed plant cells or plant, and produce transgenic plant cells or the genetically modified plants that contain through the dsRNA molecule of transcribing, process is stable.Especially, method of the present invention can comprise the recombinant precursor in the plant cell, and it can produce the dsRNA transcript with the RNA sequence height homology of insect genes group inner nucleotide sequential coding.The sequential coding of insect genes group inner nucleotide will cause the ability of insect existence and host cells infected to reduce to its negative adjusting for the survival of insect and propagation very under the situation of important function of gene.Therefore, this type of negative adjusting has caused maintenance viability of insect and propagated adverse effect, because it prevents from or reduced insect to rely on the nutrients feed from host cell, the ability of life.Utilize above-mentioned insect viability and propagated reduction, in plant cell, promoted the resistance of insect infection and/or the tolerance of raising.Gene in the insect can stage of ripe (growing up), prematurity (larva) or ovum by target.

In another embodiment, the weakening bacterial strain of the avirulence of microorganism can be used as the carrier of insect-controlling agent, and in this case, the microorganism of carrying this type of reagent is also referred to as insect-controlling agent.Can be in addition engineered to microorganism, make its nucleotide sequence of expressing target gene, producing following RNA molecule, described RNA molecule comprise with insect cell in the RNA sequence complementation found of typical case or the RNA sequence of homology.Insect is exposed to described microorganism, makes microorganism be ingested, and by RNA molecule or the direct or indirect negative accent to the target gene expression that mediates of fragment or derivatives thereof.

Perhaps, the invention provides: insect is exposed to insect-controlling agent of the present invention, and described controlling agent is included in the Spray Mixing device, is applied to the host, for example, and the surface of host plant.In a kind of exemplary embodiment, insect is transported to the insect digestive tract to the picked-up of insect-controlling agent with insect-controlling agent, is transported to subsequently in the cell in the insect bodies.In another embodiment, insect-controlling agent also can allow transporting of insect-controlling agent by alternate manner (for example injection or other physical method) to the infection of insect.In another embodiment, RNA molecule self is packed to advance synthetic matrix, polymer for example, and be applied to the host, for example surface of plant.Insect allows insect-controlling agent to be transported to insect to the picked-up of host cell, causes the negative accent to target gene among the host.

Can expect that also composition of the present invention can be comprised the into seed of plant species, it can be used as and is comprised the into expression product of the genomic recombination gene of plant cell, is perhaps comprised in the coating or seed treatment that into is applied to before plantation on the seed.The plant cell that contains recombination gene is counted as transgenic event in this article.

We believe that when making up with the transgenic event that following protection is provided, insecticidal seed treatment can provide significant advantage, and described protection is used to keep out the invasion and attack of no vertebra pest, and described incident is in the preferred validity scope at the target pest.In addition, we believe, and are as well known to those skilled in the art, have following situation, and wherein, this type of transgenic event that has in preferred validity scope is favourable.

The present invention also comprises having seed and the plant that surpasses a kind of transgenic event.This type of combination is called as " piling up " transgenic event.The described transgenic event that piles up can be the incident at same target pest, and perhaps they can be at different target pests.A kind of preferred embodiment in, have expression Cry 3 albumen or its seed that kills the ability of insect variant and also have the ability of expressing at least a other insecticide, it includes but not limited to albumen different with Cry 3 albumen and/or following RNA molecule, the sequence of the RNA that expresses in the next comfortable target pest of the sequence of described RNA molecule, when expressing at seed or from the plant cell that seed grows, it forms the double-stranded RNA structure, wherein, the target pest has caused inhibition to rna expression in the target pest cell to the picked-up of one or more cells of plant.

In another kind of preferable methods, have the transgenic event that the herbicide tolerant of providing also is provided for the seed of expressing following dsRNA ability, the sequence of described dsRNA is from the target pest.Preferably, provide the transgenic event of herbicide tolerant to provide, the incident of the resistance of N-(phosphine carboxymerhyl) glycine (the isopropyl amine salt form that comprises this type of weed killer herbicide) to glyphosate.

In the method for the invention, remove to handle the seed that comprises transgenic event with insecticide.We believe; transgenic seed (shows the biologically active at the target pest; this be kill the insect amount, transgenic seed or from the plant cell that this seed growth comes, kill the result of the production of insect dsRNA) with some chemistry or albumen insecticide the processing that seed carries out is combined; can provide beyond thought collaborative advantage to seed, comprise: provide outstanding effect protection, beyond thought to the infringements of the genetically modified plants that obtain at the target pest with this type of processing.Especially; we believe; with about 100gm some insecticide (for every 100kg seed) to about 400gm; handle expressing some transgenic seed that can form the construct of dsRNA molecule (its sequence is that one or more sequences of expressing obtain) from corn rootworm, the beyond thought outstanding protection of keeping out corn rootworm is provided.In addition, we believe that this type of combination also is useful on the corn plant of protecting the state of emergency at the infringement of unregistered land tiger.Seed of the present invention is also believed to have the character that reduces the insecticide use cost, because than the situation of not using inventive compositions and method, for obtaining the protection of requirement, can use insecticide still less.In addition, because used insecticide still less, and because its application before plantation, there is not independent field to use, we believe that method of the present invention is therefore all safer for operator and environment, and more cheap than conventional method potentially.

Referred when being " working in coordination with " when some effects, this expression comprises: the combination of transgenic event and insecticide is for the combination acts synergistically of insecticidal activity (or efficient).But, this does not represent this type of synergy is restricted to insecticidal activity, they also should comprise following beyond thought advantage, for example, reduction, the distribution of insecticide environment of the field of activity that increases, favourable activity curve (being relevant to type and quantity that infringement reduces), insecticide and application cost reduces, insecticide reduces to the personnel's of production operation and maize planting seed exposure, and other advantage well known by persons skilled in the art.

Can be used for the insecticide and the insecticide (comprising) of the present invention and method and composition of the present invention combination and use this type of method for compositions can be at for example U.S. Patent number 6 as seed treatment and coating, 551, find in 962, it incorporates this paper in full by reference into.

Have been found that the present invention is useful on the agriculture pest that protection seed and plant are kept out broad range, comprises insect, mite, fungi, yeast, mould, bacterium, nematode, weeds and parasite and saprophyte.

Preferably, seed treatment as herein described and coating are used with transgenic seed of the present invention, especially, except using to transgenic seed from the dsRNA molecule of sequence shown in SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table and SEQ ID NO:169 to the SEQ ID NO:174 or the acquisition of its sequence, also use insecticide to transgenic seed.Though we believe that seed treatment can be used to the transgenic seed that is in any physiological status, preferably, seed is in (durable) state of enough lasting stabilities, can not cause infringement during treatment process.Typically, seed is that gathered in the crops from the field, under removing from genetically modified plants and separates with any other non-spermatophyte material.Preferably, seed also will be stabilized to following degree biologically, make processing can not cause the biology infringement to seed.In one embodiment, for example, handle may be used on the following corn seed, described seed is gathered in the crops, is cleaned and be dried to water content by weight less than about 15%.In another embodiment, seed can be following seed: it is dried, and be coated with (prime) again and gone up water and/or other material, and then with carrying out drying again before the pesticide treatments or during handling.In the restriction of just having described, we believe, can processing be applied on the seed in any incident between results seed and the sowing seed.Term used herein " seed of not sowed " is used to comprise: be in seed results and any period between ground sowing seed (for the purpose of plant germination and growth).

When mentioning the seed do not sowed by insecticide " processing ", this type of processing is not used in and comprises following operation: wherein, insecticide is applied to soil, but not is applied to seed.For example, when being sowed with seed, use this type of and handle in soil band (band), " T " band or ditch dug with a plow, it is included not to be considered to the present invention.

The combination of insecticide or insecticide can " (neat) purely " be used, that is, and and without any dilution or there is other component.But typically, insecticide is applied on the seed with the form of insecticidal formulation.This prescription can contain one or more other components of wanting; it includes but not limited to; liquid diluent is used as the adhesive of pesticide substrate, is used for the filler of protection seed under stress conditions and the plasticizer that is used to improve coating elasticity, adhesion and/or ductility.In addition, for contain seldom or do not contain filler the oiliness insecticidal formulation for, may need to the prescription in add desiccant, for example, calcium carbonate, kaolin or bentonite, perlite, diatomite or any other sorbing material.The purposes of these components in seed treatment is known in the art.For example, see U.S. Patent number 5,876,739.Those skilled in the art can easily select the component wanted, are used for insecticidal formulation, and this depends on processed seed category and the specific insecticide selected.In addition, can use commercial formulation easy acquisition, known insecticides, as shown in hereinafter embodiment.

The component that insecticide of the present invention can be used as seed coating is applied on the seed.One of embodiment by adding insecticide combination of the present invention can use seed coating process known in the art and composition after improveing.For this class coating process and the equipment of its application is disclosed, for example, U.S. Patent number 5,918 is in 413,5,891,246,5,554,445,5,389,399,5,107,787,5,080,925,4,759,945 and 4,465,017.The seed coating composition is disclosed, and for example U.S. Patent number 5,939, and 356,5,882,713,5,876,739,5,849,320,5,834,447,5,791,084,5,661,103,5,622,003,5,580,544,5,328,942,5,300,127,4,735,015,4,634,587,4,383,391,4,372,080,4,339,456,4,272,417 and 4,245, in 432 grades.

The insecticide that uses in coating is those insecticides as herein described.The amount of the insecticide that uses in the processing to seed will depend on the type of seed category and active component and change, but described processing will comprise, and seed is contacted with the insecticide combination of the amount with insecticidal action.When insect is the target pest, described amount will be to have the amount of the insecticide of insect effect extremely.Scale with extremely insect effect used herein shows that the amount of insecticide can be killed the larva or the pest in pupa stage that is in growth, perhaps with continuous decrease or postpone the amount of the infringement that harmful insect produces.

Usually, the amount to the insecticide of seed application in the processing changes in following ranges: for every 100kg seed weight, approximately 100gm is to the about pesticide active ingredient of 2000gm.Preferably, the amount of insecticide is in following ranges: for the active component of the about 50gm of every 100kg seed to about 1000gm; More preferably, in following ranges: for the active component of the about 100gm of every 100kg seed to about 600gm; Further more preferably, in following ranges: for the active component of the about 200gm of every 100kg seed to about 500gm.Perhaps, the amount that has been found that the insecticide of the pesticide active ingredient that surpasses about 60gm for every 100kg seed is preferred, more preferably, surpasses about 80gm (every 100kg seed).

The insecticide that is used for handling must not suppress seed sprouting, but should can cause the period to seed or plant injury in the targeted insect life cycle, is effective in protection seed and/or plant.Usually, after planting, coating will be effectively about 0 to 120 day.

Insecticide of the present invention can be applied on the seed with the form of coating.The use of coating is effective especially when following high insecticide load (can be needed to typically handle fire-resistant pest, for example, corn rootworm), and prevention simultaneously is because the unacceptable toxicity to plant that the insecticide load that increases causes.

The coating that forms with insecticides disclosed herein preferably can move by diffusion or through matrix, and insecticide is discharged at a slow speed on every side in the media.

Outside the removing coating, one or more in the also available following compositions are handled seed: other insecticide comprises fungicide and weed killer herbicide; Herbicide-safener; Fertilizer and/or biocontrol agent.These compositions can be used as independent layer and add, and perhaps can add in the insecticide coating.

Can use traditional coating technique and machinery, insecticidal formulation is applied on the seed, for example, fluidized bed technology, roller mill method, cylinder static (rotostatic) seed processing machine and drum coater.Other method, for example the bed with mouth also can use.Seed can be by pre-classification (presized) before applied.After the coating, typically, can carry out drying, it is transferred to carry out classification in the sorter seed.These class methods are known in the art.

" insect-controlling agent " used herein or " gene containment agent " refers to specific RNA molecule, and it is made of first section RNA segment and second section RNA segment of linking to each other by the 3rd section RNA segment.First section and second section RNA segment are within the length of RNA molecule, and they are highly oppositely between mutually repeats, and connects together by the 3rd section RNA segment.Complementarity between first section and the second section RNA segment cause two sections segments in vivo or external hybridization form the ability of duplex molecule, promptly, form stem, wherein first section with second section segment in an end of every section link to each other by the 3rd section segment, form ring, make total form loop-stem structure, perhaps even more closely hybrid structure can form stem ring knotting (knotted) structure.Second section and second section segment indistinguishably, be not respectively corresponding to justice and the antisense sequences of target RNA, described RNA is that the target gene of target harmful insect transcribes, described gene can be contained by the picked-up of dsRNA molecule.Insect-controlling agent can also be the nucleic acid molecules of highly purified (or separation), more particularly, and from nucleic acid molecules or its nucleic acid fragment molecule in genomic DNA (gDNA) or cDNA library.Perhaps, described fragment can comprise littler oligonucleotides, and it has about 15 to about 250 nucleotide residues, and more preferably, about 15 to about 30 nucleotide residues." insect-controlling agent " can also refer to DNA construct, and described construct comprises nucleic acid molecules or its nucleic acid fragment molecule through separation and purifying, and described molecule is from gDNA or cDNA library." insect-controlling agent " can also refer to comprise the microorganism of this DNA construct, and described DNA construct comprises from nucleic acid molecules or its nucleic acid fragment molecule gDNA or cDNA library, that pass through separation and purifying.Phrase used herein " manufacturing insect-controlling agent " refers to following method, wherein use and (for example be easy to the recombinant DNA technology that obtains in this area, see Sambrook, et al.), prepare and to transcribe through the stable dsRNA or the recombinant DNA construction body of siRNA molecule, can transcribe through the stable dsRNA or the carrier of siRNA molecule to make up, and/or transform or make contain transcribe obtain, through the stable dsRNA or the cell or the microorganism of siRNA molecule.Method of the present invention provides the production to the dsRNA transcript, and its nucleotide sequence and target RNA sequence height homology, described target RNA sequence are that the target nucleotide sequence in the target harmful insect genome is coded.

Term used herein " genome " not only comprises the chromosomal DNA of finding in the nuclear when being used for insect or host cell, it also is included in the organelle DNA of finding in the subcellular components of cell.Therefore, DNA of the present invention is introduced in process in the plant cell and can locatees by chromosomal integration or by organelle and carry out.Term " genome " comprises chromosome and the plasmid in the bacterial host cell when being applied to bacterium.Therefore, DNA of the present invention is introduced in process in the bacterial host cell and can locatees by chromosomal integration or by the plasmid device and carry out.

The inhibition that target gene is expressed can be by quantitatively, and this is to be undertaken by measuring the albumen that endogenous target RNA or target RNA translation produced, and the consequence of inhibition can be verified by the inspection of pair cell or biological extrinsic property.The method that is used for RNA and protein quantification is well known to a person skilled in the art.It is obtainable giving ampicillin, bleomycin, chloramphenicol, gentamicin, hygromycin, card are received the multiple choices mark of resistance of mycin, lincomycinum, methotrexate (MTX), careless fourth phosphine, puromycin, miramycin, rifampin and tetracycline etc.

Some preferred embodiment in, gene expression has been suppressed at least 10%, preferably, at least 33%, more preferably, at least 50%, further more preferably, at least 80%.In particularly preferred embodiment of the present invention, the gene expression in the insect cell has been suppressed at least 80%, more preferably, and at least 90%, more preferably, at least 95%, perhaps at least 99%, make significant the inhibition take place.Significant suppress to be used to refer to enough inhibition, the minimizing that is detected of its phenotype that causes to be detected (for example, larval growth stops, paralysis or death etc.) or pairing RNA of repressed target gene and/or protein.Though In some embodiments of the present invention, be suppressed in all in fact cells of insect and take place, other preferred embodiment in, suppress only in the cell subgroup of expressing this gene, to take place.For example, if repressed gene is played a significant role in the cell in insect nutrition digestion road, intragentic inhibition just is enough to insect is applied deleterious effects to these cells.

Advantage of the present invention can include but not limited to following: be easy to dsRNA is introduced insect cell, can use the dsRNA or the siRNA of low concentration, the stability of dsRNA or siRNA and the validity that suppresses.A lot of shortcomings that the ability of the dsRNA use low concentration, that process is stable has avoided antisense to disturb.The present invention is not restricted to external use, or be restricted to special sequence composition, specific target gene group, the specific part of target gene nucleotide sequence, or specific transgenosis body or the specific method of transporting, this be with obtainable method known in the art in some run counter to, for example, antisense and common containment.In addition, genetic manipulation and the biology of non-classical genetic model in also be feasible.

In to practice of the present invention, following main points are important: the existence of transcribing the nucleotide sequence that comes from recombinant precursor is to wherein their plant cells that can express according to the present invention are harmless, and particularly the mankind are also harmless to the animal food chain.Because it is obtainable that the product of plant may absorb for the mankind, the negative accent that the target nucleotide sequence is expressed only betides in the insect.

Therefore, in order optionally to obtain the inhibition to target gene in wishing controlled insect species, preferably, the sequence homogeny of corresponding gene should be minuent in target gene and plant or the vertebrate.Preferably, sequence homogeny degree is less than about 80%.More preferably, sequence homogeny degree is less than about 70%.Most preferably, sequence homogeny degree is less than about 60%.

According to one embodiment of the present invention, a kind of nucleotide sequence is provided, its vivoexpression can cause transcribing of the stable RNA sequence of following process, the RNA numberator height homology of target gene in described RNA sequence and the insect, described RNA molecule comprise the coded RNA sequence of nucleotide sequence in the insect genes group.Therefore, after insect picked-up is through stable RNA sequence (be contained in the meals or be sprayed on the plant surface), realize negative accent to target gene corresponding nucleotide sequences in the targeted insect cell.Caused maintenance, survival, propagation, breeding and propagate deleterious effects by the negative nucleotide sequence of transferring in the insect insect.Therefore, nucleotide sequence of the present invention can be used for regulating or controlling the invasion and attack of the insect in certain scope.

According to another embodiment of the invention, a kind of nucleotide sequence is provided, its expression in microbial cell causes transcribing of following RNA sequence, the RNA numberator height homology of target gene in described RNA sequence and the insect, described RNA molecule comprises RNA sequence nucleotide sequence coded in the insect genes group.Therefore, after the stable RNA sequence of the process that contains in the insect ingested microorganisms cell, will cause the nucleotide sequence of target gene in the insect cell to be transferred by negative.Caused maintenance, survival, propagation, breeding and propagate deleterious effects by the negative nucleotide sequence of transferring in the insect insect.Therefore, nucleotide sequence of the present invention can be used for regulating or controlling the invasion and attack of the insect in certain scope.

According to another embodiment of the invention, a kind of nucleotide sequence is provided, its expression in plant cell causes transcribing of following RNA sequence, the RNA numberator height homology of target gene in described RNA sequence and the insect, described RNA molecule comprises RNA sequence nucleotide sequence coded in the insect genes group.Therefore, after the stable RNA sequence of the process that contains in the insect picked-up plant cell, will cause the nucleotide sequence of target gene in the insect cell to be transferred by negative.Caused maintenance, survival, propagation, breeding and propagate deleterious effects by the negative nucleotide sequence of transferring in the insect insect.Therefore, nucleotide sequence of the present invention can be used for regulating or controlling the invasion and attack of the insect in certain scope.

Term used herein " height homology " or " high homology ", when mentioning with acid sequence, be illustrated under the rigorous condition with SEQ ID NO:1 to the SEQ ID NO:143 shown in the sequence table in any sequence or the nucleotide sequence that can hybridize of the coded sequence shown in any sequence among SEQ ID NO:169 to the SEQ ID NO:174 or its complementary series.Under rigorous condition with SEQ ID NO:1 to the SEQ ID NO:143 shown in the sequence table in any sequence or the sequence that can hybridize of any sequence among SEQ ID NO:169 to the SEQ ID NO:174 or its complementary series, it is the sequence that allows to take place between two sequences the antiparallel comparison, two sequences can form hydrogen bond with the corresponding base on the opposite strand under rigorous condition then, to form the disome molecule, it is sufficiently stable under rigorous condition, uses approach well known to detect.Preferably, the sequence of this type of height homology and any sequence among SEQ ID NO:1 to the SEQ ID NO:143 shown in the sequence table or the contrast nucleotide sequence shown in any sequence among SEQ ID NO:169 to the SEQ ID NO:174 or its complementary series have about 65% to about 70% sequence homogeny, perhaps more preferably, about 80% to about 85% sequence homogeny, perhaps most preferably, about 90% to about 95% sequence homogeny, the sequence homogeny to about 99%.

Term used herein " sequence homogeny ", " sequence similarity shape " or " autoploidy " are used to describe the relation between two or many nucleotide sequences.The percentage of " sequence homogeny " is measured by following method between the two sequences: compare two sequences that are optimised alignment on comparison window, wherein, than control sequence (do not comprise and add or disappearance), in the comparison window part of sequence can comprise add or disappearance (promptly, breach), be used for optimization alignment two sequences.Calculate percentage by following method: measure the quantity that has the position of identical nucleic acid base or amino acid residue in the two sequences, to produce the quantity of matched position, total number of positions with in the quantity removal comparison window of matched position multiply by 100 to produce the percentages of sequence homogeny with the result.The all identical sequence in each position is considered to identical with control sequence during with the control sequence comparison, and vice versa.If article one nucleotide sequence shows the complete complementarity with second or control sequence, when observing with 5 ' to 3 ' direction, article one nucleotide sequence be considered to the second observed with 3 ' to 5 ' direction or contrast nucleotide sequence complementary series or with its complementation.In this article, all complementary the time, we say that the nucleotide sequence molecular display goes out " complementary fully " to each nucleotide in the sequence of reading with 5 ' to 3 ' direction with each nucleotide of other sequence of reading with 3 ' to 5 ' direction.To show and contrast the identical sequence of reverse complementary sequence of nucleotide sequence with the nucleotide sequence of contrast nucleotide sequence complementation.These terms and description have good detailed description in the art, are that those of ordinary skills are understandable.

" comparison window " used herein refers to, the notion segment of at least 6 continuous positions, common about 50 to about 100, more commonly, about 100 to about 150 continuous positions, wherein, two sequences is optimised after the alignment, and a sequence is compared with the control sequence with same quantity continuous position.Than control sequence (do not comprise add or disappearance), comparison window can comprise about 20% or interpolation still less or disappearance (that is, breach), is used for optimization alignment two sequences.Those skilled in the art will be with reference to Wisconsin Genetics SoftwarePackage Release 7.0, Genetics Computer Group, 575 Science DriveMadison, Wis., be used for the detailed method of sequence alignment in USA) or with reference to Ausubel et al. (1998) going through about sequence analysis.

Target gene of the present invention obtains from insect cell, and perhaps it is a foreign gene, for example, and from the exogenic heredity sequence of virus, fungi, insect or nematode etc." acquisition " refers to that sequence is all or part of from the naturally occurring nucleotide sequence of the genomic target gene of insect cell; As fruit gene is structural gene, especially, is coupled with the part of naturally occurring nucleotide sequence of the mRNA of the poly-adenosineization of one-level cap, montage, and described mRNA is that the naturally occurring dna sequence dna of finding in the cell is expressed; Perhaps and all or part of sequence of the RNA of nonstructural gene, it includes but not limited to tRNA, catalysis RNA, rRNA, Microrna etc.The nucleotide sequence of natural RNA makes if the sequence that obtains is based on, show about 80% to about 100% sequence homogeny with native sequences, and can hybridize with native sequences under rigorous hybridization conditions, sequence obtains from these naturally occurring RNA sequences so.In one embodiment, target gene comprises any sequence among SEQ ID NO:1 to the SEQ ID NO:143 shown in the sequence table or nucleotide sequence or its complementary series shown in any sequence among SEQ ID NO:169 to the SEQ ID NO:174.The dosage that transports that depends on specific target gene and dsRNA molecule, this method can be so that all or part of loss of the function of target gene, perhaps marginal any containment level of wanting.

The present invention also provides artificial DNA sequence, it can be expressed in cell or microorganism, and, it can suppress the expression of target gene in insect cell, tissue or the organ, wherein, artificial DNA sequence comprises the dsDNA molecule of one or more different IPs nucleotide sequences of encoding at least, wherein, positive sense nucleotide sequence and antisense base sequences that in the different IPs nucleotide sequence each all comprises intervening sequence and connected, the described intervening sequence dsRNA molecule of the present invention of encoding.Intervening sequence has constituted the part of positive sense nucleotide sequence and antisense base sequences, and it will be formed in the dsRNA molecule between justice and the antisense sequences.Positive sense nucleotide sequence is identical with nucleotide sequence or derivatives thereof or its complementary series height of target gene with antisense base sequences.The dsDNA molecule operationally is positioned under the control of promoter sequence, and described promoter sequence plays a role in host's cell, tissue or organ, expresses dsDNA, produces the dsRNA molecule.In one embodiment, artificial DNA sequence can obtain from the nucleotide sequence shown in SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table or SEQ ID NO:169 to the SEQ ID NO:174.

The present invention also provides artificial DNA sequence, is used for expressing at plant cell, and, along with DNA is expressed as RNA and is absorbed by the target pest, can obtain containment to the expression of target gene in harmful insect cell, tissue or the organ.DsRNA comprises one or more structural gene sequences at least, wherein, positive sense nucleotide sequence and antisense base sequences that every kind of structural gene sequence all comprises intervening sequence and connected, described interval preface forms in complementary and antisense sequences and encircles.Positive sense nucleotide sequence is identical with nucleotide sequence or derivatives thereof or its complementary series height of target gene with antisense base sequences.One or more structural gene sequences operationally are positioned under the control of one or more promoter sequences, wherein at least a protokaryon or eucaryote, particularly insect cell, tissue or organ in be exercisable.In one embodiment, artificial DNA sequence comprises the sequence of about SEQ IDNO:1 to the SEQ ID NO:143 shown in the sequence table or about SEQ ID NO:169 to SEQ ID NO:174.

Term used herein, " gene that non-natural exists ", " coded sequence that non-natural exists ", " artificial sequence " or " composite coding sequence " that are used to transcribe dsRNA of the present invention or siRNA or its fragment refer to, separate and those of the means preparation handled with the heredity that relates to any kind of, described means can be prepared the coded sequence of transcribing dsRNA of the present invention or siRNA or its fragment.This comprises coded sequence is separated from its naturally occurring state, coded sequence is handled, this is to insert, lack or replace by (1) nucleotide, (2) segment is inserted, is lacked or replaces, (3) chemosynthesis, for example deoxynucleoside phosphoramidite chemical method etc., locus specificity sudden change, to brachymemma or any other manipulation or the separating method of coded sequence.

According to this respect of the present invention, the gene order or its fragment that are used for the non-natural existence of WCR control can be cloned between the exercisable two kinds of tissue-specific promoters of transgenic plant cells, two kinds of root-specific promoters for example, described gene order or its fragment can be expressed herein, in transgenic plant cells, produce mRNA, thereby form the dsRNA molecule.The dsRNA molecule that contains in the plant tissue is absorbed by insect, thereby the expectation that obtains target gene is expressed suppresses.

The present invention also provides a kind of method, is used to obtain to comprise the nucleic acid of following nucleotide sequence, and described nucleotide sequence can be produced dsRNA of the present invention or siRNA.A kind of preferred embodiment in, the method that is used to obtain nucleic acid of the present invention comprises: (a) go to survey cDNA or gDNA library with hybridization probe, described probe comprises all or part of from the nucleotide sequence of targeted insect or its homologue; (b) identify can with the dna clone of hybridization probe hybridization; (c) isolate the dna clone of identifying in the step (b); And (d) checked order to being included in the cDNA or the gDNA fragment of separating DCRP in the step (c), wherein, the nucleic acid molecules that is checked order can the transcribe rna nucleotide sequence or its homologue whole or most.

In another preferred embodiment, the method that is used to obtain nucleic acid fragment (nucleotide sequence that wherein comprises the overwhelming majority that is used for production dsRNA of the present invention or siRNA) of the present invention comprises the steps: (a) synthetic article one and second Oligonucleolide primers, and they are with corresponding from the part of one of nucleotide sequence of targeted insect; And the article one and the second Oligonucleolide primers that (b) use step (a), the cDNA or the gDNA that exist in the amplification cloning vector insert, wherein, and the overwhelming majority of the nucleic acid molecules energy transcript invention dsRNA that amplification obtains or the overwhelming majority of siRNA.

In to practice of the present invention, target gene can be from corn rootworm (CRW), and for example WCR or SCR obtain, perhaps from causing crop plants to be compromised and any insect species of subsequently the underproduction obtains.It is considered herein that some kinds of standards can be used to select preferred target gene.Described gene is such gene: its protein product has circulating rate fast, makes dsRNA suppress to cause the quick reduction of protein level.In some embodiments, it is favourable selecting for use a small amount of drop of expression can cause the gene to the illeffects of insect.If think target wide spectrum insect species, to be chosen in the gene of high conservative between these species so.On the contrary, in order to bring specificity, In some embodiments of the present invention, select to contain between various insect species or between insect and other biology, guard the gene in the low zone of degree.In some embodiments, selecting not have the gene of the known homologue of other biology is that people want.

Term used herein " from ... obtain " refer to, can from specific special source or the special nucleotide sequence that obtains of species, though need not be directly from these special source or species.

In one embodiment, select the gene of in the insect digestive tract, expressing for use.The gene that target is expressed in digestive tract has been avoided the needs at the inner dsRNA of distribution of insect.Being used for target gene of the present invention can comprise, for example, and with those (Dow et al., 1997, J.Exp.Biol., 200:237-245 of the nucleotide sequence height homology of the known digestive tract expressing gene of coding plasma membrane proton V-ATPase protein component; Dow, Bioenerg.Biomemb., 1999,31:75-83).This protein complexes is unique energy supplier of epithelial cell example transhipment, is used for the alkalization of midgut inner chamber.V-ATPase also expresses in Ma Shi (Malpighian) pipe, described malpighian tube be the insect hindgut grow body (outgrowth), its with the similar mode of mammal kidney organ, in fluid balance and detoxifcation, play a role to xenobiontics.

In another embodiment, select the very important function of gene that relates in insect growth, growth and the breeding for use.Exemplary gene includes but not limited to, CHD3 gene and 'beta '-tubulin gene.CHD3 gene code among the Drosophila melanogaster has the albumen of ATP dependent form DNA helicase activity, and its chromatin that relates in the nuclear assembles/separate assembling.Similarly sequence also is found in the multiple biology, for example Arabidopsis thaliana, Caenorhabditis elegans and Saccharomyces cerevisiae.The albumen that beta-microtubule protein gene family coding is relevant with microcosmic, described albumen is the component part of cytoskeleton.Correlated series also is found in the multiple biology, for example Caenorhabditis elegans and ManducaSexta.

Being used for other target gene of the present invention can comprise, for example, and those of in survival, growth, growth, breeding and propagation, playing an important role.These target genes can be one of the following: lethal knocks out sudden change among household's gene, transcription factor and insect specific gene or the Drosophila.The target gene of Shi Yonging can also be from those of other biology in the present invention, for example, from nematode (for example C.elegans).In addition, being used for nucleotide sequence of the present invention also can be from following plant, virus, bacterium or fungal gene, and the function of described gene has been established in document, and its nucleotide sequence is shared the similitude of height with target gene in the insect genes group.A method according to the present present invention, for WCR control, target sequence can obtain from target WCR insect substantially.Coding and the D.v.virgifera albumen of known protein homology or its fragment, can from sequence table, find from some exemplary goal sequences in WCR cDNA library.

Nucleic acid molecules from the coding known protein homologue of D.virgifera is known (Andersen et al., US Patent Application Serial No.10/205,189).

Though the described sequence main reference of Andersen et al. WCR, in practice of the present invention, the preferred dna segment that uses with following sequence, described sequence with need controlled target pest in the corresponding sequence of gene or coded sequence have about at least 80% homogeny, perhaps about at least 90% homogeny, perhaps at least 95% homogeny, perhaps at least 98% homogeny, perhaps about at least 100% homogeny.Comparatively useless with the homogeny of target sequence less than about 80% sequence.Suppress to be specific to one or more genes of pest, the corresponding dsRNA of the sequence of described gene.Irrelevant expression of gene is unaffected.This species specificity allows pest species selectivity target in addition, thereby to being exposed to other biological not influence of the present composition.

Be used for dna segment length of the present invention for about at least 19 to about 23 nucleotide, perhaps about 23 to about 100 nucleotide, but are less than about 2000 nucleotide.

The invention is not restricted to specific gene as herein described, it also comprises following any gene, can apply illeffects to harmful insect to the inhibition of described gene.

So a lot of in the insect of the potential target controlled by the present invention, the information of the phenotype that obtains about the sequence of most of genes with from the sudden change to specific gene may be limited.Therefore, the inventor proposes, select suitable gene from harmful insect and be used for process of the present invention, can can be to model organism (for example Drosophila) by using, some other insect species, perhaps in addition the information that the research of corresponding gene obtains in the nematode species, fungal species, plant species (corresponding gene in these species is analyzed) carry out.In some cases, may by use from, for example sequence or the gene name of Drosophila, other insect, nematode, fungi or plant (wherein said gene is therefrom cloned), the garbled data storehouse, for example GenBank obtains the sequence of targeted insect corresponding gene.In case obtained sequence, can use increase gene segment in the insect of selecting suitably of PCR, be used for the present invention.

In order to obtain dna segment, design the PCR primer based on the sequence of in other insect that WCR or gene are therefrom cloned, finding from corresponding gene in the insect species.Primer is designed to: the dna segment of the sufficient length that can increase is used for the present invention.DNA (genomic DNA or cDNA) preparation comes the DNA amplification segment from insect species with the PCR primer.Amplification condition is selected to be: even can not accurately mate under the situation of target sequence at primer, amplification also can be carried out.Perhaps, can use WCR gene or other known insect genes,, clone gene (or its part) from the gDNA or the cDNA library of preparation from harmful insect species as probe.The technology that is used for implementing PCR and clones from the library is known.Based on the gene order that from WCR or other insect species, cloned in the past, from the target harmful insect, do all one can the further details of method of dna segment, provide to some extent in an embodiment.Persons of ordinary skill in the art will recognize that multiple different technology can be used for from the harmful insect species, isolating with before the corresponding gene segment of gene that separates from other species kind.

Classify based on the feed mode, may cause the damaged insect of plant to belong to three major types usually, this three class is respectively to belong to Coleoptem, Lepidoptera, Diptera, Orthoptem, Heteroptera, Ctenophalides, Arachnidiae and Hymenoptera purpose chewing type, suctorial type and boring formula insect.The chewing type insect eats the tissue of plant, and for example root, leaf, flower, bud and spray cause big infringement.Example from this big caste comprises beetle and larva thereof.WCR and SCR belong to the chewing type insect.Their larva is taken food on the root of plant, especially, on the root of corn plant, its adult blade of mainly taking food.From WCR or SCR or can be used as target from the gene of any species in the above-mentioned order and be used to carry out the present invention.

Have been found that the present invention can be used for protecting seed and plant to keep out agriculture widely pest, comprises insect, mite, fungi, yeast, mould, bacterium, nematode, weeds and parasitism and saprophyte etc.

When insect was target pest of the present invention, this type of pest included but not limited to, from the Lepidoptera purpose, for example,

Acleris spp., Adoxophyes spp., Aegeria spp., Agrotis spp., Alabamaargillaceae, Amylois spp., Anticarsia gemmatalis, Archips spp, Argyrotaenia spp., Autographa spp., Busseola fiisca, Cadra cautella, Carposina nipponensis, Chilo spp., Choristoneura spp., Clysiaambiguella, Cnaphalocrocis spp., Cnephasia spp., Cochylis spp., Coleophora spp., Crocidolomia binotalis, Cryptophlebia leucotreta, Cydia spp., Diatraea spp., Diparopsis castanea, Earias spp., Ephestiaspp., Eucosma spp., Eupoecilia ambiguella, Euproctis spp., Euxoa spp., Grapholita spp., Hedya nubiferana, Heliothis spp., Hellula undalis, Hyplumtria cunea, Keiferia lycopersicella, Leucoptera scitella, Lithocollethis spp., Lobesia botrana, Lymantria spp., Lyonetia spp., Malacosoma spp., Mamestra brassicae, Manduca sexta, Operophteraspp., Ostrinia Nubilalis, Pammene spp., Pandemis spp., Panolisflammea, Pectinophora gossypiella, Phthorimaea operculella, Pierisrapae, Pieris spp., Plutella xylostella, Prays spp., Scirpophaga spp., Sesamia spp., Sparganothis spp., Spodoptera spp., Synanthedon spp., Thaumetopoea spp., Tortrix spp., Trichoplusiani and Yponomeuta spp.;

From the Coleoptera purpose, for example,

Agriotes spp., Anthonomus spp., Atomaria linearis, Chaetocnematibialis, Cosmopolites spp., Curculio spp., Dermestes spp., Diabroticaspp., Epilachna spp., Eremnus spp., Leptinotarsa decemlineata, Lissorhoptrus spp., Melolontha spp., Orycaephilus spp., Otiorhynchusspp., Phlyctinus spp., Popillia spp., Psylliodes spp., Rhizopertha spp., Scarabeidae, Sitophilus spp., Sitotroga spp., Tenebrio spp., Triboliumspp. with Trogoderma spp.;

From the Orthoptera purpose, for example,

Blatta spp., Blattella spp., Gryllotalpa spp., Leucophaea maderae, Locusta spp., Periplanetassp. and Schistocerca spp.;

From the Isoptera purpose, for example,

Reticulitemes?ssp；

From the Psocoptera purpose, for example,

Liposcelis?spp.；

From the Anoplura purpose, for example,

Haematopinus spp., Linognathus spp., Pediculus spp., Pemphigusspp. and Phylloxera spp.;

From the Mallophaga purpose, for example,

Damalinea spp. and Trichodectes spp.;

From the Thysanoptera purpose, for example,

Franklinella spp., Hercinothrips spp., Taeniothrips spp., Thripspalmi, Thrips tabaci and Scirtothrips aurantii;

From the Heteroptera purpose, for example,

Cimex spp., Distantiella theobroma, Dysdercus spp., Euchistusspp., Eurygaster spp., Leptocorisa spp., Nezara spp., Piesma spp., Rhodnius spp., Sahlbergella singularis, Scotinophara spp., Triatomaspp., the spp. of Miridae family (for example Lygus hesperus and Lygus lineoloris), spp. of Lygaeidae family (for example Blissus leucopterus) and the spp. of Pentatomidae family;

From the Homoptera purpose, for example

Aleurothrixus floccosus, Aleyrodes brassicae, Aonidiella spp., Aphididae, Aphis spp., Aspidiotus spp., Bemisia tabaci, Ceroplasterspp., Chrysomphalus aonidium, Chrysomphalus dictyospermi, Coccushesperidum, Empoasca spp., Eriosoma larigerum, Erythroneura spp., Gascardia spp., Laodelphax spp., Lacanium corrii, Lepidosaphes spp., Macrosiphus spp., Myzus spp., Nehotettix spp., Nilaparvata spp., Paratoria spp., Pemphigus spp., Planococcus spp., Pseudaulacaspisspp., Pseudococcus spp., Psylla ssp., Pulvinaria aethiopica, Quadraspidiotus spp., Rhopalosiphum spp., Saissetia spp., Scaphoideusspp., Schizaphis spp., Sitobion spp., Trialeurodes vaporariorum, Triozaerytreae and Unaspis citri;

From the Hymenoptera purpose, for example,

Acromynnex, Atta spp., Cephus spp., Diprion spp., Diprionidae, Gilpinia polytoma, Hoplocampa spp., Lasius sppp., Monomoriumpharaonis, Neodiprion spp, Solenopsis spp. and Vespa ssp.;

From the Diptera purpose, for example,

Aedes spp., Antherigona soccata, Bibio hortulanus, Calliphoraerythrocephala, Ceratitis spp., Chrysomyia spp., Culex spp., Cuterebraspp., Dacus spp., Drosophila melanogaster, Fannia spp., Gastrophilusspp., Glossina spp., Hypoderma spp., Hyppobosca spp., Liriomysa spp., Lucilia spp., Melanagromyza spp., Musca ssp., Oestrus spp., Orseoliaspp., Oscinella frit, Pegomyia hyoscyami, Phorbia spp., Rhagoletispomonella, Sciara spp., Stomoxys spp., Tabanus spp., Tannia spp. and Tipula spp.;

From the Siphonaptera purpose, for example,

Ceratophyllus spp. and Xenopsylla cheopis, and

From the Thysanura purpose, for example,

Lepisma?saccharina。

Have been found that, when harmful insect is Diabrotica spp., especially, when harmful biology is a Diabrotica virgifera virgifera (Western corn rootworm, WCR), Diabroticabarberi (Northern corn rootworm, NCR), Diabrotica virgifera zeae (zea mexicana rootworm, MCR), Diabrotica balteata (Brazilian corn rootworm, BZR) or Brazilian corn rootworm complex (BCR, form by Diabrotica viridula and Diabroticaspeciosa) or Diabrotica undecimpunctata howardii (Southern corn rootworm, SCR) time, the present invention is particularly useful.

The present invention also is effective in the insect species that control can be pierced through plant cell and be organized and therefrom suck fluid especially, it includes but not limited to, fleahopper (plant bug) in smelly stinkbug (species of Pentatomidae family) and the Miridae family, for example western fleahopper (westerntarnished plant bug, Lygus hesperus species), fleahopper (tarnished plant bug, Lygus lineolaris species) and white peas or beans fleahopper (pale legume bug, Lygus elisus).

To the improvement of method disclosed herein, unexpectedly be particularly useful in the lepidopterous crop pest of control.

The invention provides through stable dsRNA or siRNA molecule, be used to control insect infestations.DsRNA or siRNA molecule comprise double-stranded through the polymerization ribonucleotide, and it can comprise the modification to phosphate sugar backbone or nucleosides.Modification in the RNA structure can be coupled with tail, suppresses to allow specificity heredity.

In one embodiment, can modify the dsRNA molecule, can produce the siRNA molecule by enzyme method.SiRNA can be at the effectively negative accent effect of mediation of some target genes in some insects.This kind of enzyme method can be finished (Elbashir et al., 2002, Methods, 26 (2): 199-213 by utilize the RNAse III enzyme or the DICER enzyme that exist in insect, vertebrate, fungi or the plant cell in eucaryotic RNA i approach; Hamilton andBaulcombe, 1999, Science 286:950-952).This method also can utilize the reorganization DICER or the RNAse III that are incorporated in the targeted insect cell by recombinant DNA technology to carry out, and this is that those skilled in the art are easy to know.Naturally be present in the dsRNA chain that DICER enzyme in the insect or by the recombinant DNA technology manufacturing and RNAse III can will be bigger and be cut into less oligonucleotides.The DICER enzyme can be cut into the siRNA segment with the dsRNA molecule specifically, and wherein, each siRNA segment is that about 19-25 nucleotide is long, and RNAse III enzyme is cut into the dsRNA molecule siRNA of 12-15 base-pair usually.3 ' suspension and 5 ' phosphoric acid and the 3 ' C-terminal that has 2 to 3 nucleotide by the siRNA molecule of above-mentioned any enzyme generation.SiRNA that produces by RNAse III enzyme and identical by the Dicer manufacturing in eucaryotic RNA i approach, therefore, then can be by target, and after loose by interior the degraded of intracellular rna degradation mechanism, be separated into single stranded RNA, and the RNA sequence hybridization of transcribing with target gene.What this method was can effectively degrade or remove the nucleotide sequence coded RNA sequence of target gene in the insect.The result is exactly by the silence of the nucleotide sequence of special target in the insect.The details of enzyme method is described can (2002, Nature finds in 418:244-251) at Hannon.

Utilize that of the present invention to suppress target gene through the stabilizing dsrna technology be sequence-specific, because suppress by target at heredity with RNA two body region corresponding nucleotide sequences.The RNA that contains the nucleotide sequence identical with the part of target gene is optimized for inhibition.The RNA sequence that relative target sequence has insertion, disappearance and simple point mutation also has been found inhibitory action.At aspect of performance of the present invention, preferably, the part of inhibition dsRNA and target gene is shared about at least 80% sequence homogeny, perhaps be higher than about 90% sequence homogeny, perhaps be higher than about 95% sequence homogeny, perhaps be higher than about 99% sequence homogeny, perhaps even about 100% sequence homogeny.Perhaps, two body region of RNA can functionally be defined as: can with the nucleotide sequence of the part of target gene transcript hybridization.The sequence less than total length that shows higher autoploidy can be equivalent to (compensate) long sequence that less autoploidy is but only arranged.The length of identical nucleotide sequence can be about at least 25,50,100,200,300,400,500 or about at least 1000 bases.Usually, should use the sequence above 20-1100 nucleotide, be preferred though surpass the sequence of about 200-300 nucleotide, and the sequence that surpasses about 500-1000 nucleotide is especially preferred, and this depends on the size of target gene.The present invention has following advantage: it can stand sequence variant, and described variant may cause owing to genetic mutation, bacterial strain polymorphy or evolutionary divergence.With respect to the one-level transcription product or the mRNA through processing fully of target gene, the nucleic acid molecules of introducing may not need absolute homology, may not need total length.Therefore, those skilled in the art need recognize that as disclosed herein, 100% sequence homogeny between RNA and the target gene is also nonessential for putting into practice the present invention.

The dsRNA molecule can be interior or external synthetic by body.DsRNA can be formed by the RNA chain of wall scroll self complementation, perhaps can be formed by the RNA chain of two complementations.The endogenous RNA polymerase of cell can mediate in the body transcribes, and perhaps Ke Long RNA polymer can be used in the body or in-vitro transcription.Can come target to suppress by following method: the specific transcriptional in organ, tissue or cell type; The stimulation of environmental condition (for example, infect, coerce, temperature, chemical inducer); And/or transcribe at the engineering that developmental stage or age carry out.The RNA chain can yes or no poly-adenosineization; The RNA chain can or can not be translated as polypeptide by the translating equipment of cell.

RNA of the present invention, dsRNA, siRNA or miRNA are produced by chemical method or enzyme method by those skilled in the art, and this is by manually or automatically reacting or carrying out in another organism.Also can make RNA by organic synthesis partially or completely; Can synthesize or any ribonucleotide of organic synthesis introducing by vitro enzyme through modifying.Can synthesize RNA by intracellular rna polymerase or phage rna polymerase (for example, T3, T7, SP6).Expression construct use and manufacturing is (sees, for example, WO 97/32016, U.S. Patent number 5,593,874,5,698,425,5,712,135,5,789,214 and 5,804,693) known in the art.If by chemosynthesis or synthetic, can before introducing cell, carry out purifying to RNA by vitro enzyme.For example, can from mixture, be purified into RNA by with solvent or resin extraction, precipitation, electrophoresis, chromatogram or its combination.Perhaps, can or only carry out at purifying not using RNA under the situation of minimal purifying, to avoid because the loss that sample processing causes.RNA can be dried with storage, perhaps is dissolved in the aqueous solution.Solution can contain buffer and salt, to promote the stable and/or annealing of disome chain.

For transcribing from transgenosis body or expression construct in vivo, can use regulation and control zones (for example, promotor, enhancer, silencer and poly-adenosineization) to transcribe (or many) RNA chain.Therefore, in one embodiment, the nucleotide sequence that is used for making the RNA molecule can operationally link to each other with one or more promoter sequence that has function at microorganism, fungi or plant host cell.Ideally, nucleotide sequence is placed under the control of endogenesis promoter, and described endogenesis promoter is in the host genome usually.Be in the nucleotide sequence of the present invention under the promoter sequence control that is operably connected, flank can also have extra sequence, and described extra sequence can advantageously influence the stability of its transcript of transcribing and/or obtaining.This type of sequence is usually located at the upstream of the promotor that is operably connected, and/or the downstream of expression construct 3 ' end, can be present in the downstream of promotor upstream and expression construct 3 ' end simultaneously, though only be to have sequence also to be comprised on this type of.

In another embodiment, nucleotide sequence of the present invention can comprise the reverse repetition of being separated by " intervening sequence ".Intervening sequence can be the zone that comprises following any nucleotide sequence, and if necessary, described nucleotide sequence can promote that secondary structure forms between every section repetition.In one embodiment of the invention, intervening sequence is to be used for the justice of mRNA or the part of antisense coded sequence.Perhaps, intervening sequence can comprise can with the covalently bound nucleotide of nucleic acid molecules or any combination of its homologue.Intervening sequence can comprise the nucleotide sequence of length for about at least 10-100 nucleotide, and perhaps length is about at least 100-200 nucleotide, and length is about at least 200-400 nucleotide, and perhaps length is about at least 400-500 nucleotide.

With regard to purpose of the present invention, dsRNA or siRNA molecule can obtain from CRW, and this is to realize by the target CRW gene order that obtains from corn rootworm gDNA or cDNA library or its part are carried out polymerase chain (PCR) amplification.Can prepare the WCR larva with the known method of those of ordinary skills, can extract DNA/RNA.The larva of different sizes can be used for purpose of the present invention from the 1st age to the CRW that grows up to fully, carry out DNA/RNA and extract.Genomic DNA or cDNA library can be used to pcr amplification, to produce dsRNA or siRNA.

Can use the method that obtains easily in this area then, target gene is carried out pcr amplification and order-checking.Those skilled in the art can be changed the PCR condition, form to guarantee optimum PCR product.PCR product through checking can be used as template, is used for transcribing in the body, has the justice and the antisense RNA of the Min. promotor of being included with generation.

Of the present inventionly turn over the famous person and propose, the nucleotide sequence that any insect species from Bugdom is identified and is purified into can be used for the present invention, with control WCR and other targeted insect.In one aspect of the invention, can obtain nucleic acid from species from the coleoptera species.Especially, the chrysomelid worm that can be subordinated to Diabrotica genus (coleoptera, Chrysomelidae) obtains nucleic acid, more particularly, can organize from virgifera and obtain nucleic acid of the present invention.The most especially, nucleic acid of the present invention can obtain from Diabrotica virgifera virgifera LeConte, and it is commonly called WCR.Can be used for through the nucleic acid that separates, for example identify target gene, and make up following recombinant vector that described carrier can be produced stable dsRNA of process of the present invention or siRNA, is used for protective plant and keeps out the WCR insect infestations.

Therefore, in one embodiment, the present invention comprises the nucleotide sequence through separation and purifying from WCR or Lygus, and it can be used as insect-controlling agent.Through separating and the nucleotide sequence of purifying comprises SEQ ID NO:1 to the SEQ IDNO:143 that lists in the sequence table or the sequence shown in SEQ ID NO:169 to the SEQ ID NO:174.

From WCR or other insect, can be used for nucleic acid of the present invention and also can comprise through separating and highly purified Unigenes and EST nucleic acid molecules or its nucleic acid fragment molecule.The EST nucleic acid molecules can coded polypeptide marking area, perhaps in fact, the major part of polypeptide.Perhaps, described fragment can comprise littler oligonucleotides, and described oligonucleotides has about 15 to about 250 nucleotide residues, and more preferably, about 15 to about 30 nucleotide residues.Perhaps, being used for nucleic acid molecules of the present invention can be from the cDNA library of WCR, lygus or any other no vertebra pest species.

Phrase used herein " highly purified nucleic acid ", " artificial sequence ", " through separating and highly purified nucleic acid " or " through separating and highly purified nucleotide sequence " refer to following nucleic acid, it no longer is attended by in the material that its native state follows some, perhaps any all different in its structure and the naturally occurring nucleic acid.The example of highly purified nucleic acid comprises: (1) DNA, and it has the partial sequence of naturally occurring genomic DNA molecule, but two coded sequences that its flank does not have this molecular moiety flank in the naturally occurring biological gene group of this dna molecular to exist; (2) comprised nucleic acid among carrier into or protokaryon or the eukaryotic gene group DNA, the means of including are that the molecule that obtains is all different with any naturally occurring carrier or genomic DNA; (3) independent molecule, for example cDNA, genomic fragment, the fragment or the restriction fragment that produce by polymerase chain reaction (PCR) (PCR); (4) recombinant DNA; And (5) synthetic DNA.Highly purified nucleic acid also can be made up of one or more cDNA, genomic DNA or synthetic DNA.

Can be used to obtain other nucleic acid molecules from the nucleic acid molecules of WCR, Lygus or other no vertebra pest species and its fragment, be used for the present invention, dsRNA and the siRNA molecule wanted with generation from other species.This type of nucleic acid molecules comprises following nucleic acid molecules, the complete coded sequence of described nucleic acid molecule encoding protein, and the promotor of this quasi-molecule and flanking sequence.In addition, this type of nucleic acid molecules comprises: encoding gene family member's nucleic acid molecules.Use above-mentioned nucleic acid molecules or its fragment to go to screen, can must obtain this quasi-molecule easily from D.v.virgifera or the cDNA or the gDNA library that obtain from Lygushesperus.The method that is used to make this type of library is well known in the art.

Can be used to obtain other nucleic acid molecules from the nucleic acid molecules of WCR or Lygus and its fragment, for example the nucleic acid homologue is used for the present invention, dsRNA and the siRNA molecule wanted with generation.This type of homologue comprises: the nucleic acid molecules of whole or other species of partly encoding, plant or other biological protein homology thing.Use above-mentioned nucleic acid molecules or its fragment to go to screen EST, cDNA or gDNA library, can easily obtain this quasi-molecule.The method that is used to make this type of library is well known in the art.The nucleotide sequence of this type of homologue molecule can be different with nucleotide sequence or its complementary series found in one or more sequences among SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table disclosed herein or SEQ ID NO:169 to the SEQ ID NO:174, because do not need complete complementation for stable hybridization.These nucleic acid molecules also comprise, though can may lack the molecule of complete complementarity with the nucleic acid molecules specific hybrid.In a kind of special embodiment, the method that is used for 3 ' or 5 ' RACE can be used for obtaining this type of sequence (Frohman, M.A.et at, Proc.Natl.Acad.ScL (U.S.A.) 85:8998-9002 (1988); Ohara, O.et at, Proc.Natl.Acad.ScL (U.S.A.) 86:5613-5611 (1989)).Usually, any kind of in above-mentioned nucleic acid molecules or the fragment all can be used to produce following dsRNA or siRNA, and described RNA is applicable to meals of the present invention, Spray Mixing thing or recombinant DNA construction body.

Phrase used herein " coded sequence ", " structure nucleotide sequence " or " structure nucleic acid molecules " refer to, are positioned over suitable regulating and controlling sequence and control following time, can be translated into the nucleotide sequence of polypeptide, and this is undertaken by mRNA usually.The border of coded sequence is to be determined by 5 ' terminal translation initiation codon and 3 ' terminal translation stop codon.Coded sequence can include but not limited to, genomic DNA, cDNA, EST and recombinant nucleotide sequence.

Term " recombinant DNA " or " recombinant nucleotide sequence " refer to, contain the DNA that genetic engineering is modified, and described modification is to be undertaken by the manipulation of mutagenesis, Restriction Enzyme etc.

The fragment of above-mentioned nucleic acid molecules or nucleic acid molecules or from other nucleic acid molecules of WCR can be under certain conditions specifically with other making nucleic acid molecular hybridization.If two molecular energies form antiparallel double-strandednucleic acid structure, just say two nucleic acid molecules specific hybrid mutually herein.If two nucleic acid molecules shows complete complementarity, we just say that a nucleic acid molecules is the complementary series of another nucleic acid molecules.If under traditional at least " low rigorous degree " condition, two molecular energies allow them to remain the state of mutual annealing with the hybridization mutually of enough stability, and we just say that these two molecules are " Min. complementations ".Similarly, if under traditional at least " high rigorous degree " condition, two molecular energies allow them to remain the state of mutual annealing with the hybridization mutually of enough stability, and we just say that these two molecules are complementary.Traditional rigorous condition is at Sambrook, et al. and Haymes, et al.In:Nucleic AcidHybridization, A Practical Approach, IRL Press, Washington, DC (1985). in describe to some extent.

Therefore, have to deviate from complete complementation to allow, as long as thisly deviate from the ability complete obiteration that can not make molecule form duplex structure.Therefore,, only need sequence enough complementary, can under used specific solvent and salinity, form stable duplex structure and get final product for the fragment that makes nucleic acid molecules or nucleic acid molecules is used as primer or probe.

Can promote the suitable rigorous condition of DNA hybridization to be, for example, be carried out in the 6.0x sodium chloride/sodium citrate (SSC) at about 45 ℃, then go to wash with 2.0 x SSC at 50 ℃, this is well known by persons skilled in the art, perhaps can be at Current Protocols in MolecularBiology, John Wiley ﹠amp; Sons, N.Y. (1989) finds among the 6.3.1-6.3.6.For example, the salinity in the cleaning step can be selected from: following 50 ℃ of low rigorous degree, about 2.0 x SSC, following 50 ℃ of paramount rigorous degree, about 0.2 x SSc.In addition, the temperature in the cleaning step can be from hanging down about 65 ℃ under the paramount rigorous degree of room temperature (about 22 ℃) increase under the rigorous degree.Temperature and salt can all change, and perhaps, it is constant that temperature or salinity can keep, and other variable changes.

Be used for nucleic acid of the present invention can with one or more nucleic acid molecules or its complementary series specific hybrid under medium rigorous condition from WCR, for example, about 2.0 x SSC and about 65 ℃.Being used for nucleic acid of the present invention will comprise: under the rigorous degree condition of height, can with those nucleic acid molecules of one or more specific hybrids in disclosed nucleic acid molecules among SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table or SEQ ID NO:169 to the SEQ ID NO:174 or its complementary series.Preferably, be used for nucleic acid molecules of the present invention will show with shown in SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table or SEQ ID NO:169 to the SEQ ID NO:174 or as disclosed herein one or more nucleic acid molecules have about at least 80%, perhaps about at least 90%, perhaps about at least 95%, perhaps about at least 98%, perhaps even about 100% sequence homogeny; Perhaps, being used for nucleotide sequence of the present invention will show with one or more nucleic acid molecules shown in, SEQ ID NO:1 to the SEQ ID NO:143 shown in sequence table isolated from the genomic DNA of harmful insect or SEQ ID NO:169 to the SEQ ID NO:174 and have about at least 80%, perhaps about at least 90%, perhaps about at least 95%, perhaps about at least 98%, perhaps even about 100% sequence homogeny.

Can be used for separating Diabrotica albumen homology thing or its cDNA fragment, gDNA and the nucleic acid of coding from the nucleic acid of WCR whole or most from same species or other species.About separate and identify the detailed description of the technology of nucleic acid of the present invention from cDNA and gDNA library, be disclosed among the embodiment.

Nucleic acid of the present invention can also be synthesized wholly or in part by methods known in the art, especially when the sequence of plant preference need be provided.Therefore nucleic acid of the present invention all or part of can be to use the codon of host's preference of selecting for use to synthesize.The codon of species preference can pass through, and for example, codon the most used from expressed proteins the specific host species is determined.Other modification to nucleotide sequence can cause mutant to have the activity of slight change.

A part of the present invention provides a kind of system that transports, and is used for transporting insect-controlling agent to insect.DsRNA that process of the present invention is stable or siRNA molecule can be introduced directly into the cell of insect, perhaps be incorporated into extracellular chamber, void space, lymphatic system, digestive system, be incorporated into the circulatory system of insect, this is undertaken by orally ingestible or utilizable other means of those skilled in the art.Be used for comprising: with the direct mixture of the food of RNA and insect by the method for oral introducing, and following engineering method, wherein, the species that are used as food have passed through engineered, expressed dsRNA or siRNA, it is fed raise then to be influenced insect.In one embodiment, for example, dsRNA or siRNA can pass through microbial expression, and microorganism can be applied to plant surface or by physical means, for example inject introducing root, stem.In another embodiment, can carry out genetically engineeredly to plant, make its expression be enough to kill the dsRNA or the siRNA of the amount of known insect that can infection plant.

Especially, in WCR, put into practice when of the present invention, the midgut that be incorporated into through stable dsRNA or siRNA in the insect bodies can be obtained the desirable inhibition to target gene.As indicated above, dsRNA or siRNA molecule can be comprised into meals or are covered on the meals, can be absorbed by insect.Under any circumstance, dsRNA of the present invention is provided in the meals of target pest.Target pest of the present invention will show about 4.5 to about 9.5 or about 5 to about 8.5 or about 6 to about 8 or about 6.5 to about 7.7 or about 7.0 digestive tract pH.The digestive tract of target pest is defined as the following position in the pest in this article, in this position, the food that pest absorbed is exposed to the environment of energy favorable for absorption dsRNA molecule of the present invention, thereby and can not meet with extremely to making the hydrogen bond division between the dsRNA two strands form the pH of single chain molecule.

In addition, with regard to the purpose of insect infestations in the controlling plant, the dsRNA that insect is controlled usefulness by spray applications is transported to the means that plant surface provides another kind of protective plant.In this case, can be fermented with the bacterium that produces and accumulate dsRNA by engineered, fermented product is filled a prescription to using compatible spray product with common agricultural.Described prescription can comprise: efficient blade covers required suitable sicker and wetting agent, and is used to protect dsRNA to avoid the UV protectant of UV infringement.Examples of such additives is commonly used in the biological insecticide industry, also well known to a person skilled in the art.Similarly, the prescription that is used for the soil application can comprise following granular recipe, and it is used as the bait of soil harmful insect (for example, corn rootworm) larva.

Also can predict, the dsRNA that the available mode consistent with the conventional agriculture practice filled a prescription and produced by chemistry or enzymatic synthesis is used as being spray product, with the control insect infestations.Described prescription can comprise: efficient blade covers required suitable sicker and wetting agent, and is used to protect dsRNA to avoid the UV protectant of UV infringement.Examples of such additives is commonly used in the biological insecticide industry, also well known to a person skilled in the art.This type of application can with other insecticide of spraying (yes or no based on biology) application combination, with keep out insect feed infringement aspect improve protection to plant.

The present inventor proposes, and the bacterial isolates of producing insecticidal protein can be used to produce the dsRNA that is used for insect control purpose.These bacterial strains show the insect control character of raising.Multiple different bacterial host can be used to produce insect control dsRNA.Exemplary bacterium can comprise E.coli, B.thuringiensis, Pseudomonassp., Photorhabdus sp., Xenorhabdus sp., Serratia entomophila and relevant Serratia sp., B.sphaericus, B.cereus, B.laterosponis, B.popilliae, Clostridiumbifermentans and other Clostridium species, or other forms the Gram-positive bacteria of spore.

The invention still further relates to and be used for the recombinant DNA construction body of expressing in microorganism.Can use methods known in the art, the exogenous nucleic acid that therefrom can transcribe out target RNA is introduced microbial host cell, for example, bacterial cell or fungal cell.

Nucleotide sequence of the present invention can be introduced in the protokaryon and eucaryon host of wide scope, produces through stable dsRNA or siRNA molecule.Term " microorganism " comprises protokaryon and eukaryotic microorganisms species, for example bacterium and fungi.Fungi comprises yeast and a fungi etc. is arranged.Illustrative prokaryotes, existing Gram-negative also has gram-positive, comprises Enterobacteriaceae, for example Escherichia, Erwinia, Shigella, Salmonella and Proteus; Bacillaceae; Rhizobiceae, for example Rhizobium; Spirillaceae, for example photobacteria, Zymomonas, Serratia, Aeromonas, Vibrio, Desulfovibrio, Spirillum; Lactobacillaceae; Pseudomonadaceae, for example Pseudomonas and Acetobacter; Azotobacteraceae, Actinomycetales and Nitrobacteraceae.Eucaryote comprises fungi, for example Phycomycetes and Ascomycetes, and it comprises yeast, for example, Saccharomyces and Schizosaccharomyces; And the Basidiomycetes yeast, for example, Rhodotorula, Aureobasidium, Sporobolomyces etc.

With regard to regard to the purpose of insect protective plant, a large amount of microorganisms of known blade face (surface of plant leaf) that inhabits the important crop of multiple difference and/or rhizosphere (soil around the plant root) also can be to be used for recombinant precursor disclosed herein is handled, bred propagation, preserves, transports and/or the desirable host cell of mutagenesis.These microorganisms comprise bacterium, algae and fungi.What have special interest is microorganism, for example, bacterium, for example following genus: Bacillus (comprises following kind and subspecies: B.thuringiensis kurstaki HD-I, B.thuringiensis kurstaki HD-73, B.thuringiensis sotto, B.thuringiensisberliner, B.thuringiensis thuringiensis, B.thuringiensis tolworthi, B.thuringiensis dendrolimus, B.thuringiensis alesti, B.thuringiensisgalleriae, B.thuringiensis aizawai, B.thuringiensis subtoxicus, B.thuringiensis entomocidus, B.thuringiensis tenebrionis and B.thuringiensis san diego); Pseudomonas, Erwinia, Serratia, Klebsiella, Zanthomonas, Streptomyces, Rhizobium, Rhodopseudomonas, Methylophilius, Agrobacterium, Acetobacter, Lactobacillus, Arthrobacter, Azotobacter, Leuconostoc and Alcaligenes; Fungi, particularly yeast, for example, following genus: Saccharomyces, Cryptococcus, Kluyveromyces, Sporobolomyces, Rhodotorula and Aureobasidium.What have special interest is this type of plant bacterial species on every side, Pseudomonassyringae for example, Pseudomonas fluorescens, Serratia marcescens, Acetobacterxylinum, Agrobacterium tumefaciens, Rhodobacter sphaeroides, Xanthomonas campestris, Rhizobium melioti, Alcaligenes eutrophus and Azotobacter vinlandii; And the yeast species around the plant, for example, Rhodotorularubra, R.glutinis, R.marina, R.aurantiaca, Cryptococcus albidus, C.diffluens, C.laurentii, Saccharomyces rosei, S.pretoriensis, S.cerevisiae, Sporobolomyces roseus, S.odorus, Kluyveromyces veronae and Aureobasidium pollulans.

The bacterium recombinant DNA carrier can be a cyclic plasmid linear or sealing.Carrier system can be single carrier or plasmid, or two or more carriers or plasmid, and they contain the total DNA that will be introduced in the bacterial host genome together.In addition, bacteria carrier can be an expression vector.Nucleic acid molecules shown in SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table or SEQID NO:169 to SEQ ID NO:174 or its fragment can, for example, be fit to be inserted in the carrier, described carrier is under the control of suitable promotor, described promotor plays a role in one or more microbial hosts, to drive the coded sequence connected or the expression of other dna sequence dna.For this purpose, a lot of carriers all are obtainable, will depend primarily on band to the selection of suitable carrier and be inserted into the size of the nucleic acid in the carrier and the particular host cell that will transform with carrier.Every kind of carrier all contains various ingredients, and this depends on its function (DNA amplification or expressible dna) and the particular host cell compatible with it.Being used for carrier component that bacterium transforms generally includes but is not limited to one or more of following component: burst, origin of replication, one or more selectable marker genes and the inducible promoter that allows foreign DNA to express.

Expression and cloning vector contain the selection gene usually, and it is also referred to as selected marker.What this gene code was grown on selective medium survives or the necessary albumen of growing through transformed host cell.The typical following albumen of gene code of selecting, described albumen energy: (a) give to antibiotic or other toxin, for example, the resistance of ampicillin, neomycin, methotrexate (MTX) or tetracycline, (b) supply auxotrophy, or (c) provide the crucial nutrients that can't from complex medium, obtain, for example, for Bacilli, the gene of encoding D-alanine racemase.These can be produced the albumen of giving drug resistance by heterologous protein or its fragment success cell transformed, thus can survival in selecting processing.

The expression vector that is used to produce mRNA also can contain following inducible promoter, described promotor can be by the host bacteria bio-identification, and be operably connected with following nucleic acid, described nucleic acid for example, the nucleic acid of encoding D .v.virgifera mRNA or its interesting fragment.The inducible promoter that is suitable for bacterial host comprises the beta-lactamase promotor, E.coli bacteriophage lambda PL and PR promotor, and E.coli galactose promotor, arabinose promotor, alkaline phosphatase promoter, tryptophan (trp) promotor and lactose operon promotor and variant and hybrid promoters, for example, tac promotor.But other known bacteria-induction type promotor also is suitable.

When mentioning regulating and controlling sequence and structure nucleotide sequence, term " is operably connected " and refers to, regulating and controlling sequence causes the expression of the structure nucleotide sequence that links to each other to be regulated and control." regulating and controlling sequence " or " control element " refers to be positioned at the nucleotide sequence of structure nucleotide sequence upstream (5 ' non-coding sequence), centre or downstream (3 ' non-translated sequence), and it can have influence on opportunity and the level or the quantity of the transcribing of dependency structure nucleotide sequence, RNA processing or stability or translation.Regulating and controlling sequence can comprise promotor, translation homing sequence, intron, enhancer, loop-stem structure, the sub-binding sequence of containment and poly-adenosine recognition sequence etc.

Perhaps, expression vector can be integrated into bacterial genomes with integration vector.Typically integration vector contains and allows at least a sequence of the bacterial chromosome homology of vector integration.Integration looks like that in carrier DNA and the bacterial chromosome reorganization between the homologous dna causes.For example, use the integration vector that makes up from the DNA of multiple Bacillus bacterial strain can be integrated into Bacillus chromosome (EP 0,127,328).Integration vector also can comprise bacteriophage or transposons sequence.Suicide type carrier also is known in the art.

Structure to the suitable carrier that contains one or more elements of listing above utilizes the recombinant DNA technology of standard to carry out.To being cut, add tail, and be connected to the required plasmid desirable form of generation again through plasmid or the dna fragmentation that separates.The example of obtainable bacterial expression vector includes but not limited to, multi-functional E.coli clone and expression vector, for example, Bluescript ^TM(Stratagene, La Jolla, CA), wherein, for example, D.v.virgifera albumen or its fragment can be connected into carrier, described connection be with meet be used for beta galactosidase amino terminal Met and subsequently the mode of the reading frame of seven residues carry out, produce hybridization albumen thus; The pIN carrier (Van Heeke and Schuster, 1989, J.Biol.Chem.264:5503-5509) etc.

Typically, the yeast recombinant precursor comprises one or more in the following component: promoter sequence, fusion partner sequence, homing sequence, translation termination sequence, selected marker.These elements can be combined into expression cassette, and expression cassette can be held in the replicon, extra-chromosomal element (for example, plasmid) for example, and it can be stablized and remains among the host (for example yeast or bacterium).Replicon can have two cover dubbing systems, allows it to be held in thus, for example, is used in the yeast expressing, and is used for clone and amplification among the prokaryotes host.The example of this type of yeast-bacterium shuttle vector comprises YEp24 (Botstein et al., 1979, Gene, 8:17-24), pCl/1 (Brake et al., 1984, Proc.Natl.Acad.Sci USA, 81:4642-4646) and YRpl7 (Stinchcomb et al., 1982, J.MoI.Biol., 158:157).In addition, replicon can be the plasmid of high or low copy number.High copy number plasmid will have about 5 copy numbers to about 200 scopes usually, typically, and about 10 to about 150.It is about at least 10 that the host of containing high copy number plasmid will preferably have, more preferably about at least 20 copies.

Useful yeast initiating sequence can obtain by the gene of enzyme from encoding metabolic pathway.The example of this genoid comprises alcohol dehydrogenase (ADH) (EP 0 284044), enolase, glucokinase, glucose-6-phosphate isomerase, glyceraldehyde-3-phosphate dehydrogenase (GAP or GAPDH), hexokinase, phosphofructokinase, 3-phosphoglycerate mutase and pyruvate kinase (PyK) (EP 0 3215447).The yeast PHO5 gene of coding acid phosphatase also provides useful promoter sequence (Myanohara et al., Proc.Natl.Acad.Sci.USA, 80:1,1983).In addition, natural non-existent synthetic promoter also can be used as Yeast promoter and plays a role.The example of this type of hybrid promoters comprises the ADH regulating and controlling sequence (U.S. Patent number 4,876,197 and 4,880,734) that links to each other with GAP transcriptional activation zone.Other example of hybrid promoters comprises, by the regional promotor of forming (EP0 164556) of the transcriptional activation of carbohydrate-splitting enzyme gene (for example GAP or PyK) on ADH2, GAL4, GAL10 or the PHO5 gene regulation combined sequence.In addition, Yeast promoter can comprise: have and combine with the yeast rna polymerase and naturally occurring promotor initial ability of transcribing, non-yeast source.

(for example, those of coding carbohydrate-splitting enzyme) example is well known by persons skilled in the art for transcription terminator and other terminator sequence that can be discerned by yeast.

Perhaps, expression construct can be integrated into the yeast genes group with integration vector.Typically, integration vector contains at least a sequence with the yeast chromosomal homology that allows vector integration, and preferably contains the two kind homologous sequences of flank in the table construct.Integration look like that the reorganization between the homologous dna causes in carrier and the yeast chromosomal (Orr-Weaver et al., 1983, Methods in Enzymol., 101:228-245).Integration vector can be at the specific gene seat in the yeast, and this is by selecting suitable homologous sequence to comprise that into carrier is realized.Described Orr-Weaver et al. sees above.One or more expression construct can be integrated, possibly, the level of the recombinant protein that influence produces (Rine et al., 1983, Proc.Natl.Acad.Sci.USA, 80:6750).The chromosome sequence that comprises in the carrier can be used as single segment and is present in the carrier, this can cause the integration of whole carrier, perhaps it can be used as two segments existence, adjacent segment homology in described two segments and the chromosome, the expression construct of flank in carrier, it can cause only is the stable integration of expression construct.

The present invention also proposes, and nucleotide sequence of the present invention is transformed into plant, makes one or more dsRNA molecular energies suppress horizontal expression with pest.Use the obtainable method in this area, can easily prepare conversion carrier.Conversion carrier comprises one or more following nucleotide sequence, described sequence can be transcribed into the RNA molecule, and with one or more nucleotide sequence height homology and/or complementations of insect genes group coding, make: when insect absorbs from the RNA that one or more nucleotide sequence molecules are transcribed, can be born accent at least a expression in each nucleotide sequence in the insect genes group.

Conversion carrier also can be represented the dsDNA construct, and in addition, it also can be taken as recombinant molecule, insect-controlling agent, genetic molecule or chimeric (chimeric) genetic constructs.Mosaic heredity construct of the present invention can comprise, for example, encode one or more antisense transcripts, one or more just transcripts, above-mentioned every kind one or more nucleotide sequence, wherein, from its all or part of homology of all or part of and following RNA molecule of transcript, described RNA molecule comprises RNA sequence nucleotide sequence coded in the insect genes group.

In one embodiment, plant conversion carrier is through the dna molecular of separation and purifying, wherein comprises the startup word that operationally links to each other with one or more nucleotide sequences of the present invention.Nucleotide sequence is selected from the group that is made of SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table or SEQ ID NO:169 to SEQ ID NO:174.Nucleotide sequence comprises following segment, and the RNA's that exists in its coding target pest rna transcription basis is all or part of, also comprises all or part of reverse repetition of target pest RNA.The dna molecular that comprises expression vector also can contain functional intron sequences (its be positioned the upstream of coded sequence or even among coded sequence), described molecule can also contain five casts aside (5 ') untranslated homing sequence (promptly, UTR or 5 '-UTR), it is positioned between promotor and the translation initiation site.

Plant conversion carrier can contain from the sequence more than a kind of gene, allows thus to produce more than a kind of dsRNA, is used for suppressing two or more expression of gene of target pest cell.One of ordinary skill in the art will readily recognize that the dna segment one-tenth unitary composite capable of being combined dna segment that has corresponding to the sequence of the sequence that exists in the different genes, be used for expressing genetically modified plants.Perhaps, can be modified the plasmid of the present invention that contains at least a dna segment, this is undertaken by extra dna segment is inserted between enhancer and promotor and the terminator sequence in proper order.Be used for suppressing in the insect-controlling agent of the present invention of several genes in design, treat that suppressor can obtain from same insect species, to strengthen the efficient of insect-controlling agent.In some embodiments, gene can obtain from different insects, to widen effective insect scope of reagent.When at containment or at expressing and during the combination target several genes of containment, can be according to Fillatti, number of patent application US 2004-0029283 elaboration is made polycistron DNA element with disclosed.

When going to transform under the situation of plant with nucleotide sequence of the present invention, to select for use to show the following promotor of following ability, described promotor can drive the expression of coded sequence in this specific plant species.The promotor that has function in different plant species is well known in the art.The example that is used in the promotor of express polypeptide in the plant is, Odell et al. (1985, Nature313:810-812) described induction type, virus, synthetic or constitutive promoter, and/or by the promotor from time regulation and control, space regulation and control and space-time regulation and control.Preferred promotor comprises the CaMV35S promotor and the FMV35S promotor of enhancing.With regard to purpose of the present invention, for example, for the optimum control at the species of root feed, the highest level that preferably obtains these genes in plant root is expressed.A large amount of root strengthens promotors to be identified, their be known in the art (Lu et al., 2000, J.Plant Phys., 156 (2): 277-283; U.S. Patent number 5,837,848 and 6,489,542).Typically, recombinant DNA carrier of the present invention or construct will comprise selected marker, and it can give the selection phenotype on plant cell.Selected marker also can be used for selecting the plant or the plant cell of the exogenous nucleic acid that contains code book invention polypeptide or albumen.Mark can encode biocide resistance, antibiont resistance (for example, card receive mycin, G418 bleomycin, hygromycin etc.) or Herbicid resistant (for example, glyphosate etc.).The example of selected marker includes but not limited to, coding card is received the neo gene of mycin resistance, can select at using card to receive mycin, G418 etc.; The bar gene of coding bialaphos resistance; The mutant epsp synthase gene, its glyphosate resistance of encoding; Nitrilase gene, it gives the resistance to Brominal; Mutant acetolactic acid sy nthase gene (ALS), it gives the resistance to imidazolone or sulphur urea; And the DHFR gene of anti-methopterin.

Recombinant vector of the present invention or construct also can comprise selection markers.Selection markers can be used to monitor and express.Exemplary selection markers comprises, beta-glucuronidase or uidA gene (GUS), its known enzyme (Jefferson, 1987, Plant Mol.Biol, Rep.5:387-405 that multiple chromophoric substrate is arranged that encode; Jefferson et al, 1987, EMBO is J.6:3901-3907); R-locus gene, the product (Dellaporta et al, 1988, Stadler Symposium11:263-282) that its coding can be regulated and control the generation of anthocyania pigment in the plant tissue (redness); Beta-lactamase gene (Sutcliffe et al., 1978, Proc.Natl.Acad.Sci 75:3737-3741), the known enzyme that multiple chromophoric substrate (for example, PADAC, color development cynnematin) arranged of this gene code; Luciferase genes (Ow et al., 1986, Science254:856-859); The xylE gene (Zukowsky et al., 1983, Proc.Natl.Acad.Sci50:1101-1105), and its coding catechol dioxygenase, described enzyme can transform the catechol of color development; Alpha-amylase gene (Ikatu et al., 1990, Bio/Technol.8:241-242); Tyrosinase cdna (Katz et al., 1983, J.Gen.Microbiol.129:2703-2714), its coding can be oxidized to tyrosine the enzyme of DOPA and DOPA quinone, and DOPA quinone polymerization subsequently (condense) is a melanin; Alpha-galactosidase, the α-galactose substrate of its energy catalysis color development.

Usually, preferably in Plant Genome non-specific position introduce functional recombinant DNA.Under special circumstances, can insert the recombinant DNA construction body by site-directed integration.Have the known multiple fixed point recombination system that can make implant have function, it comprises United States Patent (USP) 4,959,317 disclosed cre-lox and United States Patent (USP) 5,527,695 disclosed FLP-FRT.

In the practice, in any single transformation experiment, DNA only is introduced in the target cell of little percentage.The gene of coding selected marker is used to provide the efficient system that is used for identifying these cells that are stabilized conversion, and described conversion is by receiving the transgenosis DNA construct and its genome that is integrated into them being realized.Preferred marker gene provides the selected marker of giving the resistance of selective reagent (for example, antibiotic or weed killer herbicide).Any weed killer herbicide that plant of the present invention can have its resistance all is the useful reagent that is used for selected marker.May be exposed to selective reagent by cell transformed.In the population of survivaling cell, will be following cell, wherein, usually, resistance is given gene and is integrated, and enough allows the horizontal expression of cell survival.But pair cell is further tested, with the stable integration of checking foreign DNA.Normally used selected marker comprises and giving those of antibiotic resistance, for example card is received mycin (nptII), hygromycin B (aph IV) and gentamicin (aac3 and aacC4), perhaps to those of Herbicid resistant/tolerance, for example to careless ammonium phosphine (bar or pat), glyphosate (EPSPS) and AMPA (phnO).The example of this type of selected marker is described in United States Patent (USP) 5,550318,5,633, in 435,5,780,708 and 6,118,047.Provide the selection markers that transformant is carried out visual evaluation also can use, for example, express coloured or fluorescin () gene or express the gene or the uidA gene (GUS) of beta-glucuronidase for example, luciferase or green fluorescent protein (GFP), known its has multiple chromophoric substrate.

Preferred plant conversion carrier comprise Ti-plasmids from Agrobacterium tumrfaciens (for example, U.S. Patent number 4,536,475,4,693,977,4,886,937,5,501,967 and EP 0 122 791).Agrobacterium rhizogens plasmid (or " Ri ") also can use, and they are known in the art.Other preferred plant conversion carrier comprises Herrera-Estrella (1983, Nature 303:209-213), Bevan (1983, Nature304:184-187), Klee (1985, Bio/Technol.3:637-642 and EP 0 120516 disclosed those.

Be used for comprising any method in a large amount of means known in the art by introduce method and composition that the recombinant DNA construction body transforms plant to Plant Genome.A kind of method that is used to make up through plant transformed is the microinjection blast technique, as United States Patent (USP) 5,015, and 580,5,550,318,5,538,880,6,153,812,6,160,208,6,288,312 and 6,399,861 is described.The another kind of method that is used to make up through transforming plant is the conversion of Agrobacterium mediation, as United States Patent (USP) 5,159, and 135,5,824,877,5,591,616 and 6,384,301 is described.Perhaps, can use other non-Agrobacterium species, for example, Rhizobium and show other prokaryotic of following ability, their can infection plant's cell, heterologous nucleotide sequence is introduced the genome of infected plant cell.

Can DNA construct of the present invention be introduced target plant by well known to a person skilled in the art multiple traditional transformation technology.With regard to the purpose of the conversion of Agrobacterium mediation, suitable plant conversion carrier comprises the carrier that obtains from the Ti-plasmids of Agrobacterium tumrfaciens.Except that the plant conversion carrier of Agrobacterium mediation, other method also can be used to DNA construct of the present invention is inserted in the plant cell.These class methods can include but not limited to, for example, use liposome, and electroporation increases the absorption of dissociative DNA, bombard transport and use virus or the pollen that carry out dissociative DNA by microinjection and transform.

Can make up other genetic elements with of the present invention through any nucleic acid in the nucleic acid that separates by permanent or expedient, for example promotor, intron, enhancer and untranslated homing sequence etc. are incorporated in the plant cell.Can make coding coleoptera species RNA, or from the RNA of boring formula and suctorial type insect species, perhaps any nucleic acid molecules of D.v.virgifera RNA or Lygus Hesperus RNA preferably, and be introduced into plant cell by the means that allow in plant cell, to produce the dsRNA molecule, one or more specific dsRNA of insect amount extremely are provided in the meals of target harmful insect.

Term " transgenic plant cells " or " genetically modified plants " refer to, contain the plant cell or the plant of exogenous nucleic acid, and described exogenous nucleic acid can obtain from WCR, or obtain from different insect species or any other non-insect species.Genetically modified plants also are used for comprising the offspring (descendants (decedent), descendant etc.) of any generation of this type of transgenosis, the perhaps seed of any generation of all these type of genetically modified plants, wherein, described offspring or the seed that comprises the dna sequence dna of encode RNA of the present invention, sRNA, dsRNA, siRNA or its fragment also is importance of the present invention.

Typically, the genetically modified plants of using the Agrobacterium method for transformation to form contain the single simple recombinant DNA sequence that is inserted in the chromosome, and it is called as transgenic event.These type of genetically modified plants can be called as: about the exogenous array that inserts, heterozygosis.The genetically modified plants of isozygotying for the transgenosis body can obtain by following method: independent separate (independent segregant) genetically modified plants that will contain single exogenous gene sequence, for example, the F0 plant and himself carries out sexual mating (selfing), to produce the F1 seed.In the F1 seed that produces 1/4th will be for the transgenosis body heterozygosis.Make the F1 seed sprouting, just produced the plant that can be checked by heterozygosity, typically, use SNP test or heat amplification test to carry out, described test allows the difference (that is zygosity test) between heterozygote and the homozygote.With heterozygosis plant and himself or another kind of heterozygosis plant hybridization, only produce the heterozygosis offspring.

Except plant directly being transformed, can hybridize with second plant species that lacks this construct by first plant species that will have the recombinant DNA construction body and prepare genetically modified plants with the recombinant DNA construction body.For example, the recombinant DNA that is used for the gene containment can be introduced in the first plant species strain, the influence that described strain can be transformed, generation can with the genetically modified plants of the second plant species incross, penetrate into the second plant species strain with the recombinant DNA that will be used for gene containment.

Can be by putting into practice the genetically modified plants that the present invention makes, include but not limited to alfalfa, dill, apple, apricot, artichoke, rocket salad, asparagus, avocado, banana, barley, beans, beet (beet), blackberry, blueberry, blueberry, cabbage, brussels sprouts, cabbage, leaf mustard, muskmelon, carrot, cassava, cauliflower, celery, cherry, coriander, oranges and tangerines, the little oranges and tangerines of Ke Laimenshi, coffee, corn, cotton, cucumber, pesudotsuga taxifolia, eggplant, hare's-lettuce, wide leaf lettuce, eucalyptus, fennel, fig, cucurbit, grape, shaddock, Hami melon, yam bean, Chinese grooseberry, lettuce, leek, lemon, bitter orange, torch pine, mango, melon, mushroom, nut, oat, okra, onion, tangerine, decorate and use plant, pawpaw, parsley, pea, peach, peanut, pears, pepper, persimmon, pine tree, pineapple, plantain, Lee, pomegranate, white poplar, potato, pumpkin (pumpkin), Wen Bai, pine, witloof, radish, raspberry, paddy rice, naked barley, Chinese sorghum, the south pine, soybean, spinach, pumpkin (squash), strawberry, beet (sugarbeet), sugarcane, sunflower, Ipomoea batatas, storax, mandarin orange, tea, tobacco, tomato, turf, vining plant, watermelon, wheat, Chinese yam and Xiao Hu's melon plant.

In practice, the present invention can with other insect control proterties combination in the plant, be used to increase proterties with what obtain to want to the control of insect infestations.With utilizing the insect control and the combination of different binding modes, the genetically modified plants of protecting at insect can be provided, it has outstanding lasting stability than the plant of using single insect control proterties, reduces because develop the probability that resistance in the field.

In the past many decades, the insect mechanism of killing of B.thuringiensis crystalline protein has been carried out extensive studies.Show that only after picked-up albumen, albumin crystal albumen just can be poisonous to the larva form of insect.In the lepidoptera larva, alkaline pH in the insect midgut and proteolytic enzyme meeting soluble protein make the poisonous component of insect is discharged thus.These toxic components destroy midgut epithelial cells, cause insect to stop feed, and final, cause insect death.Former at this point thereby speech, verified B.thuringiensis toxin be from being effectively in the process of handling multiple harmful insect, and be environmentally safe insecticide.Coleoptera and hemipteran, and most likely, diptera, lygus bug and other boring formula and suctorial type insect have shown the enteron aisle pH of little acid, so it is inoperative to above-mentioned pest to be effective in the Bt toxin of keeping out the lepidoptera larva.The enteron aisle pH of the little acid of these insects is also believed composition of the present invention more friendly, do not desiring to be restricted under the situation of particular theory, seem, the alkaline pH of lepidoptera larva enteron aisle is reason (the Fire et al. U.S. Patent number 6 that the attempt failure of dsRNA effect is showed in attempt before, 506,559; Mesa et al. patent publication No. US2003/0150017; Rajagopal et al., 2002, J.Biol.Chem.277:46849-46851; Tabara et al., 1998, Science 282:430-431).Therefore we believe that dsRNA method disclosed herein should preferentially be used for controlling plant and the composition of coleoptera, diptera, Hemiptera, lygus bug, boring formula and suctorial type insect.Method and composition shown in this paper is particularly useful at the gene of containing to come in the following insect of target, and described insect shows about 4.5 to about 9.5, about 5.0 to about 9.0, about 5.5 to about 8.5, about 6.0 to about 8.0, about 6.5 to about 7.7 or about 6.8 to about 7.6 or about 7.0 enteron aisle pH.But, show about 7.5 to about 11.5, or about 8.0 to about 11.0, or the insect of about 9.0 to about 10.0 enteron aisle pH and other pest species, for example the lepidopterid larva also falls within the scope of the present invention.When in the larva meals, providing when being specific to the dsRNA that suppresses lepidoptera larva gene with one or more Bt albumen, this is especially correct, when providing with threshold value or the level that is higher than threshold value, Bt albumen can be according to conventional route to this lepidoptera larva toxigenicity.Have the existence of one or more Bt toxin of toxicity for insect species of the same race, will effectively reduce enteron aisle pH, provide stable environment, to apply their containment effects to the harmful insect target gene at double stranded rna molecule.

The dsRNA construct that the process of one or more generation dsRNA molecules of the present invention is stable makes up with one or more insecticidal proteins in the meals of target harmful insect, and it will be useful making dsRNA and insecticidal protein toxic to same harmful insect.Insecticidal protein can obtain from B.thuringiensis, also can be from other biological acquisition that can produce insecticidal protein known in the art, for example, the bacteria paragenesis body of entomopathogenic nematode (for example, Photorhabdus sp., Xenorhabdus sp.), Serratia entomophila and relevant Serratia sp., B.sphaericus, B.cereus, B.laterosporus, B.popilliae, Clostridium bifermentans and can show insecticidal matter other form the Gram-positive bacteria of spore.Similarly, also propose, the stable dsRNA construct of two or more different processes that produces dsRNA molecule of the present invention can be provided in single plant species together, to guarantee the lasting stability of insect control phenotype.The same gene of these dsRNA molecular energy targets is used for silence, and perhaps, the different gene of target is used for silence.Two or more different dsRNA can make up in same plant, and every kind of dsRNA has toxicity to different harmful insects, do not have which kind of dsRNA toxic to same insect species.

Can predict, some combination through stable dsRNA construct and one or more insects control protein gene will produce synergy, can strengthen the insect control phenotype of genetically modified plants.When the insect biologic test that utilizes artificial meals or whole plants tissue to carry out can be used for determine using dsRNA and insect control albumen about larva dead or growth inhibiting dose response.Those skilled in the art can be checked the mixture of dsRNA molecule and insect protein in biologic test; to identify active combination; described combination is to have synergitic and be (Tabashnik, 1992) that people want at the application in the insect protective plant (deployment).Reported the concertedness (summary is referring to Schnepf et al., 1998) of killing harmful insect between the different insect control albumen.Can predict, have concertedness between some dsRNA and between some dsRNA and some insect control albumen.

Can predict, the combination of dsRNA will disclose the beyond thought toxicity at some harmful insect.Rajagopol et al (2002, J Biol Chem.277:46849-46851) report is fed the larva of raising to lepidoptera pest S.litura with dsRNA, for allowing the gene silencing of coding midgut aminopeptidase not act on.What deserves to be mentioned is that the alkaline pH environment of typical lepidoptera midgut is friendly environment for dsRNA, because the sex change of RNA disome under alkaline pH will be supposed to can cause degrading rapidly.Be inserted into the hole that the B.thuringiensis toxin protein in the midgut epithelium film forms, caused midgut pH neutralization (summary is seen Gill, 1995, Mem.Inst.Osaldo Cruz, Rio de Janeiro, 90:69-74).Therefore, only can in lepidoptera midgut epithelium film, form temporary transient ion channel and can not cause dead B.thuringiensis toxin to be enough to midgut pH is reduced to the level that more helps absorbing by midgut epithelial cell dsRNA.As an example, known Cry1Ac albumen is at the beet armyworm, Spodoptera exigua be not effective toxin (Chambers et al, 1991, J.Bacteriol.173:3966-3976).But the temporary transient reduction of the midgut pH that Cry1Ac albumen causes will be useful on the stable dsRNA of picked-up altogether, make them be useful on the target gene of reticent S.exigua, and the means of this harmful insect of beyond thought control are provided thus.Employing can be upset any albumen of lepidopterid midgut epithelial cells ion regulation and control, no matter whether it can kill insect, can observe this effect, this also is useful to coleoptera, diptera, Hemiptera, lygus bug and other boring formula and suctorial type harmful insect etc.

Some insecticidal proteins from B.thuringiensis, Cyt albumen for example, the temporary transient opening that can cause sensitive insect larva midgut epithelium film, this is owing to the formation in structural hole or because (the Butko that the generality class abstergent activity of albumen causes, 2003, Appl.Environ.Microbiol.69:2415-2422).This type of opening even can assist the dsRNA molecule pass midgut epithelial cell under the protein concentration of suboptimization dead concerning causing.Can predict, can cause any albumen of temporary transient opening in the insect epithelial membrane, no matter whether can kill insect, can both assist the dsRNA molecule to enter insect cell, promote the cell silence.

The nucleotide sequence or its fragment or its complementary series that provide among SEQ ID NO:1 to SEQ ID NO:143 shown in the sequence table or SEQ IDNO:169 to the SEQ ID NO:174 can " be provided " in multiple medium, to assist use.This type of medium also can provide its subgroup, and the form of this subgroup allows those skilled in the art that sequence is checked.

The agricultural product goods that contain one or more sequences of the present invention, and the agricultural product goods of making from the recombinant plant that contains one or more nucleotide sequences of the present invention or seed as embodiments of the present invention by particularly including.The agricultural product goods that contain one or more sequences of the present invention include but not limited to; meat, oil, grain that pulverize or whole or plant seed; the any food product that perhaps comprises any meat, oil, following that pulverize or whole grain, described grain are to contain the recombinant plant of one or more sequences of the present invention or seed.In one or more agricultural product that this paper comprises or agricultural product goods, the detection of one or more sequences of the present invention is proved, agricultural product or agricultural product goods are made of genetically modified plants, described genetically modified plants are designed to express one or more nucleotide sequences of the present invention, are used for controlling by the gene containment method of using the dsRNA mediation purpose of insect infestations.

In a kind of application of present embodiment, nucleotide sequence of the present invention can be recorded on the computer-readable medium." computer-readable medium " used herein refers to: the expression medium that exists conscientiously, can pass through calculator direct reading and visit.This type of medium includes but not limited to: magnetic-based storage media, floppy disk for example, hard disk, storage medium and tape; Optical storage medium, for example CD-ROM; Electronic storage medium, for example RAM and ROM; The computer document of optical character identification form, and the crossbred of mentioned kind, for example, magnetic/optical storage medium.It will be readily apparent to those skilled in the art that any known computer-readable medium can be used to make following product at present, described product comprises the nucleotide sequence of the present invention that is recorded on the computer-readable medium.

" record " used herein refers to, is used for the method for storage information on computer-readable medium.Those skilled in the art can easily adopt any at present known method to come recorded information on computer-readable medium, comprise the medium of nucleotide sequence information of the present invention with generation.To those skilled in the art, multiple different data store organisation is obtainable, is used to make the computer-readable medium of the nucleotide sequence of minute book invention thereon.Selection to the data storage medium usually will be based on selecting the means that visit the information of being stored for use.In addition, multiple different data processor program and form can be used for nucleotide sequence of the present invention is stored on the computer-readable medium.Sequence information can be showed in the word processing text document, with the software that can obtain by commercial sources, for example WordPerfect and Microsoft Word format it, perhaps it can be shown as the form of ASCII text document, be stored in the database application, for example DB2, Sybase, Oracle etc.Those skilled in the art can must adopt any amount of data processor structured format (for example, text document or database) easily, to obtain to record the computer-readable medium of nucleotide sequence information of the present invention thereon.

The computer software of the sequence information that provides in permission those skilled in the art access computer computer-readable recording medium is that the public is obtainable.In the Sybase system, carry out BLAST (Altschulet al., J.Mol.Biol.215:403-410 (1990)) and BLAZE (Brutlag, et al, Comp.Chem.17:203-207 (1993)) software of searching algorithm can be used to identify the open reading frame (ORF) in the sequence, for example, provided herein, contain and from the Unigene and the EST of the autoploidy of other biological ORF or protein.This type of ORF is the fragment of coded protein in the sequence of the present invention, can be used for producing commercial important protein matter, for example, be used for that amino acid is synthetic, metabolism, transcribe, the enzyme of translation, RNA processing, nucleic acid and protein degradation, protein modification and dna replication dna, restriction, modification, reorganization and reparation.

The present invention also provides the system that contains sequence information as herein described, especially, and the computer based system.This type systematic is designed to: can identify the commercially important fragment in the nucleic acid molecules of the present invention." computer based system " used herein refers to be used to analyze hardware device, software equipment and the data storage device of nucleotide information of the present invention.The Min. hardware device of computer based of the present invention system comprises central processor unit (CPU), input equipment, output equipment and data storage device.Those skilled in the art can easily instruct, and anyly in the present obtainable computer based system all are suitable for the present invention.

The most preferably length of target sequence is about 10 to about 100 amino acid, or about 23 to about 300 nucleotide residues.

" object construction primitive (motif) " used herein or " target primitive " refer to, any sequence or the combined sequence rationally selected, and wherein, the 3-d modelling that forms when the based target primitive is folding is selected one or more sequences.Plurality of target primitive known in the art.Protein target primitive includes but not limited to, enzyme active sites and burst.The target set nucleic acid primitive includes but not limited to, promoter sequence, cis-acting elements, hairpin structure and inducible expression element (protein binding sequence).

Embodiment

The inventor has identified the method that is used to control no vertebra pest invasion and attack in this article, and this is undertaken by double stranded ribonucleic acid molecule is provided in the pest meals.Surprisingly, the inventor discloses, when being absorbed by pest, double stranded ribonucleic acid molecule can play a role, and suppresses the biological function of pest, cause in the following characteristics one or more: the pest feed reduces, the pest survival rate reduces, pest death, and differentiation and the growth of pest are suppressed, the reduction or the disappearance of the sexual propagation ability of pest, muscle forms, the formation of juvenile hormone, the regulation and control of juvenile hormone, ion regulation and control and transhipment, the maintenance of cell membrane gesture, amino acid bio is synthetic, amino acid degradation, sperm forms, pheromones synthetic, pheromones sensing, the formation of feeler (antennae formation), wing forms, the formation of leg, grow and differentiation the formation of ovum, the larva maturation, the formation of digestibility enzyme, synthesizing of hemolymph, the maintenance of hemolymph, neurotransmission, cell division, energy metabolism, breathe and apoptosis, and any component of eukaryotic cytoskeletal structure, for example, exciting albumen and tubulin.Any or any combination can cause the effective inhibition to the pest invasion and attack in these characteristics, under the situation to the harmful biology of plant, to the inhibition of plant invasion and attack.For example, when being used as when offering the dietary composition of one or more double stranded ribonucleic acid molecules plant, that contain the amount that is enough to suppress pest with local mode, be used as seed treatment, use as the soil around the plant, when perhaps the recombinant DNA molecules that exists in plant cell by plant was produced, the biological attack harmful to plant can unexpectedly reduce dramatically.When being applied to list kind pest, the embodiment shown in this paper is used to set forth the present invention.But, those skilled in the art will recognize that, method among the embodiment, prescription and idea are not made the usefulness of restriction, its institute that can be used for consuming following food source has or not vertebra pest species, or within it portion some key characters of playing a role relevant with containment with pest, described food source is can be by prescription for containing the pest inhibitor of q.s, and it is made of at least a or multiple double stranded rna molecule.

Embodiment 1

Present embodiment has been described the evaluation to following nucleotide sequence, when described nucleotide sequence is provided in the corn rootworm meals with the form of double stranded rna molecule, is useful on the control corn rootworm.

From whole larva and make up corn rootworm cDNA library from the midgut segment of cutting (LIB 149, LIB 150, LD33027, LIB3373), obtain nucleotide sequence information and (see that Andersen et al. is filed in the U.S. Patent Application Serial Number 10/205 on July 24th, 2002,189, its integral body is incorporated into this paper by reference especially).In addition, from being in different developmental phases and the whole larva of different time each developmental stage, come the construction cDNA library, with the quantity of maximization from the different est sequences of Diabrotica species.Library LIB5444 and LIB5462 are constructed in the mRNA storehouse that is obtained by the Western corn rootworm larva from first age (1 gram) and the 3rd age (2.9 gram) respectively.By being inserted in the liquid nitrogen, that the insect that obtains is freezing rapidly.Remaining in-20 ℃ mortar and the pestle grinding insect, temperature keeps by in refrigeration on the dry ice and/or add liquid nitrogen ground to fine powder up to tissue and realize in mortar.Use

Reagent (Invitrogen) according to manufacturers instruction, extracts RNA.(Dynal Inc. NY), according to manufacturers instruction, isolates Poly A+RNA from total RNA preparation to use Dynabeads Oligo dT.Use SuperScript ^TMPlasmid System (Invitrogen) comes the construction cDNA library from Poly A+RNA.Using chromatogram that cDNA is carried out size separates.The fourth stage and level V segment are collected, and be connected into pSPORT1 carrier (Life Technologies Ind., Gaithersburg MD) between Sal1 and the Not1 restriction enzyme enzyme recognition site, transforms into E.coli DH10B electroreception attitude cell by electroporation.The first instar larvae library has produced about 420,000 colony forming units.The third-instar larvae library has produced about 2.78 x10 ⁶Individual colony forming unit.Wash bacterium colony from flat board, evenly mix, pour the Tris-EDTA buffer solution again into by simple concussion from LIB 149, LIB150.In the material that washes half is loaded into 10% glycerine, divides and puts into freezing tubule, is stored in-70 ℃.Second half is used to produce plasmid DNA with Quiagen trace purification column or its product of equal value.Divide the threading micro-centrifuge tube with purified plasmid DNA, be stored in-20 ℃.

Indivedual amplifications are from the bacterium colony of Diabrotica virgifera cDNA library LIB5444 and LIB5462 in the high viscosity medium.Under 37 ℃, 500ml LB medium (contains the 0.3%SeaPrep agarose

With the 50mg/l carbenicillin) in the stirring flat board placed separately, mixing is from about 200,000 colony forming units of LIB5444 with from 600,000 colony forming units of LIB5462, in water/ice bath, cooled off 1 hour rapidly then, make bacterial clump evenly suspend.At 30 ℃ the library through inoculation was cultivated 42 hours then.After the incubation, pair cell carries out 5 minutes mixing on the stirring flat board.Then in the centrifugal bottle with media transfer to two 250ml.10,000xg handled 10 minutes, the precipitum cell.From bottle, shift out medium, cell is suspended in again in the LB medium of 20ml altogether, wherein contain the carbenicillin of 50mg/l.Add methyl-sulfoxide to 10%, so that cell is remained freezing state.Increased in two kinds of libraries, to every milliliter 10 ⁸Finally tiring of individual colony forming unit.The sample of combination Diabrotica virgifera cDNA library LIB5444 and LIB5462, in through aseptic distillation and deionized water, it is adjusted to the DNA concentration of about 1.25 micrograms of every microlitre, divides and put into 25 freezing tubules, each freezing tubule contains the DNA of about 8.75 micrograms.Applicant/inventor on June 10th, 2004 with these sample preservations to being positioned at 10801 University Boulevard, Manassas, the American Type Culture Colleciton (ATCC) of VirginiaUSA ZIP 20110-2209, it is called as LIB5444/62.ATCC provides the preservation receipt to the applicant, and it specifies the ATCC preserving number is PTA-6072.

Substantially produce the method in corn rootworm cDNA library according to mentioned above being used to, preparation corn rootworm HMW cDNA library, i.e. LIB5496 and LIB5498.Make up library LIB5496 and LIB5498 from the mRNA storehouse that (1 gram) Western corn rootworm larva obtains by first age (1 gram) and the 3rd age respectively.In brief, rapid freezing insect by milling, becomes fine powder with freezing insect in mortar and pestle in liquid nitrogen.Use Reagent (Invitrogen) according to manufacturers instruction, extracts RNA.(Dynal Inc. NY), according to manufacturers instruction, isolates Poly A+RNA from total RNA preparation to use Dynabeads Oligo dT.Use SuperScript ^TMPlasmid System (Invitrogen) makes up HMW cDNA library from the Poly A+RNA of 20 micrograms.On 1% Ago-Gel in TAE, cDNA is carried out size separate.Collect the cDNA in 1Kb to the 10Kb scope, connect between the Sal1 and Not1 restriction site of pSPORT1 carrier into, transform into E.coli DH10B electroreception attitude cell by electroporation.LIB5496 has produced about 3.5 x 10 ⁶Individual colony forming unit.LIB5498 has produced about 1.0 x 10 ⁶Individual colony forming unit.Indivedual amplifications are from the bacterium colony of corn rootworm HMW cDNA library LIB5496 and LIB5498 in the high viscosity medium.Under 37 ℃, 500ml LB medium (contains 0.3% SeaPrep agarose

With the 50mg/l carbenicillin) in the stirring flat board placed separately, mix about 600,000 colony forming units from LIB5496 and LIB5498, cooling 1 hour rapidly in water/ice bath then makes bacterial clump evenly suspend.At 30 ℃ the library through inoculation was cultivated 42 hours then.After the incubation, pair cell carries out 5 minutes mixing on the stirring flat board.Then in the centrifugal bottle with media transfer to two 250ml.10,000xg handled 10 minutes, the precipitum cell.From bottle, shift out medium, cell is suspended in again in the LB medium of 20ml altogether, wherein contain the carbenicillin of 50mg/l.Add methyl-sulfoxide to 10%, so that cell is remained freezing state.Increased in two kinds of libraries, to every milliliter 10 ⁸Finally tiring of individual colony forming unit.Obtain the cDNA sequence information of insertion from corn rootworm species specificity plasmid library.

Andersen et al. corn rootworm library and produce about 18,415 independent est sequences from the additional sequences in LIB5444 and LIB5462 library is initial, it is by about 1.0x 10 ⁷Individual nucleotide residue constitutes.The average length of est sequence is about 586 nucleotide residues.These est sequences are used to the bioinformatics algorithm, obtained the assembling of contig (contig) sequence, this is called as the UNIGENE sequence in this article, can not be called as singlet (singleton) in this article by the individual est sequence of overlapping homogeny and the assembling of other est sequence.Then LIB5444 and LIB5462 library are carried out the more order-checking of the degree of depth, obtain extra individual est sequence.Will be from the library, be that the est sequence that LIB149, LIB150, LIB3027, LIB3373, LIB5444, LIB5462, LIB5496 and LIB5503 obtain is showed in the sequence table, from SEQ ID NO:1 to SEQ ID NO:143 and SEQID NO:169 to SEQ ID NO:174.

If possible, will separate the est sequence that obtains from CRW cDNA library and be assembled into the UNIGENE group, the Unigene sequence of these assemblings is showed in the sequence shown in the sequence table.UNIGENE be gene location bunch, it forms overlapping in single est sequence carries sequence homogeny zone, to form bigger sequence.Every nucleotide sequence shown in the sequence table is analyzed, identified the existence of open reading frame.The amino acid sequence information that to infer from open reading frame and the known amino acid sequence information that can obtain from public database relatively, to infer the degree of amino acid sequence and these known amino acid sequence homogenies or similitude.If any, use the biological function relevant, add following note for the amino acid sequence of inferring from cDNA library nucleotide sequence information with known amino acid sequence in the public database.Note provides protein (may express from the specific gene that the provides specific cDNA sequence) function information of hint property, but this and indecisive result.Annotation information based on hint property, some cDNA sequence is accredited as: coding may relate to the albumen of some biological functions in the corn rootworm cell, described function is very important to life, be necessary perhaps, may relate to perhaps that cell is complete, cell maintenance, fertility etc. the health of guaranteeing cell and survival.

Isolate some cDNA sequences from this cDNA sequence subgroup that may encoding proteins, may cause the morbidity or the death of CRW or other invertebral living creature species cell to their inhibition.Then these sequences are used for the dsrna construct molecule, comprise into CRW meals.

It is right to design hot amplimer based on the cDNA sequence of reporting in the CRW cDNA library.Primer to or be built as a pair of nucleotide sequence, each right member of primer shows the complete complementarity with justice or antisense sequences.Make up some primers to sequence, make each member of this centering show the sequence that contains T7 phage rna polymerase promotor at its 5 ' end, as nucleotide site 1 among the SEQ ID NO:5 for example to shown in the nucleotide site 23.Preferably, use genomic DNA, increase for the first time to carrying out high-fidelity, produce first amplicon with the first kind of primer that lacks the T7 promotor as template.Preferably, cDNA or mRNA sequence are used as template, are used for the dsRNA molecule that synthetic the present invention uses, because eukaryotic gene group sequence is considered to contain non-existent sequence in the mature rna molecule in this area.To be used as template the hot amplified reaction for the second time from the first amplicon sample of high-fidelity amplified reaction generation for the first time then, with the second pair of primer that contains the T7 promoter sequence to producing second amplicon, wherein, contain in 5 ' end of every chain of second amplicon or wherein be embedded with the T7 promotor.Obtain the complete nucleotide sequence of second amplicon with both direction, itself and nucleotide sequence at the cDNA report are compared, if present, point out the difference between the two sequences.Usually, use genomic DNA as the sequence of template preparation be used to obtain the significance level containment as the further use of dsRNA molecule and inconsistent, because the variation of non-existent genome sequence in mRNA or cDNA sequence is arranged.

Typically, the in-vitro transcription reaction contains the about 1 linearisation dna profiling to about 2 micrograms, from the T7 polymeric enzyme reaction buffer solution of 10X concentrate, the t7 rna polymerase of ribonucleotide ATP, CTP, GTP and UTP (wherein concentration be every kind 50 to 100mM) and 1 unit.According to manufacturers instruction, carry out the RNA polymerase reaction in about 37 ℃ of incubation a period of times (several minutes to a few hours), this depends on used RNA polymerase.Usually, reaction carries out about 2 to about 6 hours, is used to transcribe the template sequence that reaches about 400 nucleotide most, and reaches 20 hours, is used to transcribe the template sequence of length greater than about 400 nucleotide.Reaction is heated to 65 ℃, 15 minutes, to stop rna transcription.The precipitated rna transcription product is washed in ethanol, and the air drying is suspended in it in water that does not contain RNAse again, to concentration be every milliliter of about 1 microgram.Utilize most of transcript of reverse T7 promotor strategy (being summarized as mentioned) to produce double-stranded RNA in the responsive transcription in vivo, but, by purified RNA is heated to 65 ℃, slowly cools to room temperature then and just obtained the double-stranded RNA of high yield to guarantee the correct annealing of justice and antisense RNA segment.At 37 ℃ the double-stranded RNA product is carried out one hour incubation with DNAse I and RNAse then, to remove any DNA or the single stranded RNA that exists in the mixture.According to manufacturers instruction (AMBION MEGASCRIPT RNAiKIT), purifying double-stranded RNA product on pillar is suspended in 10mMTris-HCl buffer solution (pH7.5) again with it or does not contain in the water of RNAse, to the concentration of every microlitre 0.1 to 1.0 microgram.

The double-stranded RNA sample is directly joined in each hole of containing the insect meals of above pointing out, perhaps before joining the insect meals, it is modified.To the modification of double-stranded RNA according to manufacturer provide at RNAse III (AMBION CORPORATION, Austin, Texas) or DICER (specification California) carries out for STRATAGENE, La Jolla.RNAse III has produced the disome of 21 and 22 nucleotide to the digestion of double-stranded RNA, it contains 5 ' phosphorylation end and has the 3 ' C-terminal that 2-3 base hangs, be similar to disome short interfering rna (siRNA) fragment of about 21-26 base-pair, this is Hamilton et.al. (Science, 1999,286:950-952) with Elbashir et.al. (Genes ﹠amp; Development, 2001, dicer enzyme that 15:188-200) identify, in the eucaryon approach is made.This short interfering rna disome of collecting is further purified, sample is analyzed, to measure integrality and the efficient that disome forms with polyacrylamide gel electrophoresis.Come the purity and the quantity of working sample then under the wavelength of 250 nanometers by spectrophotometric method, untapped sample is stored in-20 ℃, is used for further use.

The biologic test that the sample of siRNA or total length double-stranded RNA (dsRNA) is used to use the target pest of selected quantity to carry out.According to following flow process, the various dose of dsRNA or siRNA is applied on the artificial meals of corn rootworm as overlapping.From CropCharacteristics, Inc., Farmington, Minnesota obtains the ovum of Diabroticavirgifera virgifera (WCR).In soil, in 24 ℃, 60% relative moisture, fully down dark, the WCR ovum of non-resting stage is carried out about 13 days cultivation.At the 13rd day, the soil that will contain the WCR ovum was placed in the sieve between #30 and the #60 order, uses high pressure garden water pipe flush away soil.The surface of ovum carried out desinsection (disinfest) in three minutes by bubble in LYSOL, give a baby a bath on the third day after its birth time, wash once, washes extra three times with sterilization again with 10% formalin solution with aqua sterilisa.The ovum of handling in this way is suspended in the sterilization coffee strainer, at 27 ℃, 60% relative moisture, down dark fully, hatching is spent the night.

Substantially according to Pleau et al. (Entomologia Experimentalis et Applicata, 2002,105:1-11) the described insect meals of making have wherein been made following change.The SERVA agar of 9.4 grams are suspended in 540 milliliters of purified water, stir and disperse fully until agar.Water/agar is mixed and heated to boils,, topple over into WARING blender then to dissolve agar fully.Blender is remained low speed, and join the corn root of 62.7 gram BIO-SERVDIET mixtures (F9757), 3.75 gram freeze-drying, 1.25 milliliters of non-polluted edible pigment and 0.6 milliliter of formalin in the agar mixture of heat this moment.Be 9.0 by adding 10% potassium hydroxide storage liquid with the mixture pH regulator then.On magnetic heat of stirring flat board, with the magnetic splash bar that uses sterilization NALGENE coating, continue to be mixed with the liquid dietary of high speed to about 600 ml volumes, it is remained about 48 ℃ to about 60 ℃, and it is separated into 200 microlitre aliquots in each hole of titer plate at the bottom of FALCOM 96 hole circles.In the biological exhausting cupboard (biohood) of sterilization, make the meals in the flat board solidify and the air drying.

Use running fire type micropipettor, get the test specimen of 30 (30) microlitre volumes, wherein contain the control reagent or the double-stranded RNA of varying number, it is covered insect meals surface in each hole.After the application test sample, the insect meals are allowed to keep reaching one and a half hours (one half hour) in the biological exhausting cupboard of sterilization, so that diffusion of reagents is advanced meals, and allow the meals dry tack free.In each hole, put into a WCR newborn larvae with paintbrush.Use the MYLAR seal plate then, ventilate with insect needle.At every kind of dosage, 12-72 insect larvae to be tested, quantity depends on experimental scheme.At 27 ℃, 60% relative moisture and complete dark are carried out 12-14 days cultivation to the biologic test flat board down.Time point at 12-14 days is to the following quantity record in addition of survival larva of every kind of dosage.Use suitable microbalance,, measure the larva quality at the larva of every survival.Use

4 statistical softwares (SAS Institue, 1995) analyze data, use Dunnet ' s to check and carry out complete factorial ANOVA, with the effect (P＜0.05) of seeking processing than untreated control.Carry out Tukey-Kramer (post hoc) check afterwards, come relatively more all processing (P＜0.05).

Following nucleotide sequence is initial as obtained (the Andersen et al. of cDNA sequence that identifies in corn rootworm midgut cDNA library, the same), use it for the dsrna construct molecule, be used for upchecking feeding and raise the inhibition effect of double stranded rna molecule the pest biological function at the pest meals.

The Chd3 homologous sequence

Identify the CHD gene of coming out in multiple eucaryote, its corresponding albumen is considered to play a role as the chromatin reconstruct factor.Term CHD from three kinds of sequence homology domain: chromo (the modification person of chromosome organization) domain, the SNF2-relational coiling found in the CHD albumen mould/ATPase domain and DNA binding structural domain, all believed for every kind and can be given different chromatin related activity.Based on the whether existence of another kind of sequence homology domain (PHD Zinc finger domain, typically, relevant with the chromosome related activity), CHD albumen is divided into two classes.The CHD3 associated protein has the PHD Zinc finger domain, but the CHD1 associated protein is not then.Experiment is observed and has been hinted the effect of CHD3 albumen in containment is transcribed, and it has been shown as in some species and has contained the composition of histone as the complex of subunit.The deacetylation of histone is with to transcribe inactivation relevant; so CHD3 albumen is implied to be: utilize character as the composition of histidine deacetylase complex; can be as transcribing containment agent play a role (Ogas et al., 1999, PNAS 96:13839-13844).Therefore, the containment synthetic to CHD3 albumen can be used as useful target, at the inhibition to no vertebra pest with double chain RNA mediate.

The corresponding CRW midgut of SEQ ID NO:4 cDNA nucleotide sequence, its amino acid sequence translation is noted as: with Drosophila melanogaster CHD3 amino acid sequence (GenBank numbers AF007780) homology.SEQ ID NO:5 and SEQ ID NO:40609 correspond respectively to: forward and reverse genome amplification primer (be primer to), described primer are used to produce the amplicon from crw genomic dna, the cDNA that produces from CRW mRNA storehouse or from class libraries from then on.The sequence of this type of amplicon is corresponding to the part of the CRW gene of encoding D .melanogaster CHD3 amino acid sequence homologous body.SEQ ID NO:5 contains T7 polymerase promoter sequence (nucleotide 1-23) at its 5 ' end, the CRW genome primer sequence (forcibly being appointed as the forward primer sequence) shown in the nucleotide of 24-45 position links to each other among described promoter sequence and the SEQ ID NO:5, its corresponding to the 31st shown in the SEQID NO:4 to the 52nd nucleotide.SEQ ID NO:6 contains the T7 polymerase promoter sequence at its 5 ' end, shown in the nucleotide of 1-23 position.The T7 promoter sequence links to each other with the cdna reverse group primer sequence of mandatory appointment at its 3 ' end, and it is corresponding to the 24-44 position nucleotide shown in the SEQID NO:6, and the reverse complementary sequence of described sequence is shown in 298-319 position nucleotide among the SEQ ID NO:4.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:5 and SEQ ID NO:6 form, generation comprises the amplicon of 335 base-pairs of the nucleotide sequence shown in the SEQ ID NO:7, it is corresponding to the part of the following albumen of coding in the CRW genome, and described albumen shows the homogeny with Drosophila melanogaster CHD3 amino acid sequence about 66%.The nucleotide of the 1-23 position shown in the SEQ ID NO:7 and the nucleotide reverse complementary sequence of 314-335 position are corresponding to the terminal arbitrarily T7 promoter sequence of amplicon.The genome nucleotide that the amplification shown in 313 nucleotide of the 24th nucleotide to the obtains among the SEQID NO:7 is in fact corresponding to the cDNA nucleotide sequence that is in the news shown in 319 nucleotide of the 31st nucleotide to the among the SEQ ID NO:4, just except following difference: among the SEQID NO:4 the 63rd, 87,117,177,198,213,219-220,246, it is respectively T that 249 and 261 nucleotide is reported as, T, G, G, G, T, T, T, C, C and A, and the relevant position when comparing with SEQ ID NO:7 is the 56th, 80,110,170,191,206,212-213,239,242 and 254 nucleotide contain C, C, A, A, A, C, A, C, G, A and G.This difference is corresponding to the cDNA sequence and about 4% the difference the nucleotide sequence composition between the amplicon sequence that the genomic DNA template produces of report in the past, and this may consistent less than 99% accuracy (aforementioned Andersen et al.) with the cDNA sequence of reporting in the past.

The amplicons cloned that shows the sequence of corresponding SEQ ID NO:7 is advanced the plasmid vector that can duplicate in E.coli, reclaim the plasmid DNA of q.s, transcribe to allow carrying out external t7 rna polymerase from terminal arbitrarily embedding convergence (convergent) T7 promotor of cloned sequence.Produce double-stranded RNA, carry out biologic test; Article one, the RNA segment by about the 24th nucleotide among the SEQ ID NO:7 at least the sequence shown in about the 313rd nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:7), other RNA segment is about the 313rd nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:7, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:4.

In biologic test, be parallel to the CHD3 sequence, other nucleotide sequence that obtains from CRW is also checked, the nucleotide sequence that comprises the CRW equivalent that is noted as the following albumen of to encode, described albumen for example, the beta-tubulin, 40kDa V-ATPase protein subunit, elongation factors albumen EF1 α and EF1 α 48D, 26S proteosome subunit p28 albumen, juvenile hormone EH albumen, rely on the chloride channel albumen that expands, Robison ester 1-apodehydrogenase, actin 42A albumen, ADP-ribosylation factor 1 albumen, transcription factor IIB, chitinase protein and ubiquitin are in conjunction with (conjugating) enzyme.

Beta-tubulin homologous sequence

Tubulin is the important structure component of various kinds of cell inner structure in all eukaryotics, is mainly used in the formation microtubule.The inhibition that microtubule forms in the pair cell can cause catastrophic effect, comprises, and to the interference that the mitosis spindle forms, the obstruction of pair cell division etc.Therefore, the containment that tubulin is formed can be the useful target of the inhibition of double chain RNA mediate.

The beta-tubulin correlated series that obtains from CRW is identified, to be used for the present invention.SEQ ID NO:18 is corresponding to CRW midgut cDNA nucleotide sequence, its amino acid sequence translation is noted as: with Manduca sexta beta-1-tubulin amino acid sequence homeologous, and with Drosophila melanogaster beta-1-tubulin amino acid sequence (GenBank numbering be respectively AF030547 and M20419) homeologous.SEQ IDNO:19 and SEQ ID NO:20 correspond respectively to forward and reverse genome amplification primer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon is all or part of corresponding to the CRW gene of coding beta-tubulin.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:19 and SEQ ID NO:20, respectively at 1-23 position nucleotide.24-44 position nucleotide correspondence shown in the SEQ ID NO:19 is in the 96-116 position nucleotide shown in the SEQ ID NO:18.The reverse complementary sequence of the 24-44 position nucleotide correspondence sequence shown in the nucleotide of 428-448 position in SEQ ID:18 shown in the SEQ ID NO:20.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:19 and SEQ ID NO:20 form, produced the amplicon of 339 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:21, it is in fact corresponding to the following genomic part of CRW of coding, described albumen shown with Drosophila melanogaster and Manduca sexta in the height homogeny of the beta-tubulin homologue that exists.Nucleotide sequence shown in the SEQ ID NO:21 is in fact corresponding to the nucleotide sequence shown in the nucleotide of 96-448 position among the SEQ ID NO:18.Do not observe sequence difference between the corresponding sequence in genome amplification subsequence and cDNA sequence.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:21 is advanced plasmid vector, reclaim the plasmid DNA of q.s, transcribe to allow carrying out external t7 rna polymerase from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:21 at least the sequence shown in about the 376th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:21), reverse complemental RNA segment, or antisense strand is about the 376th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:21, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:18.

40kDa V-ATPase homologous sequence

Energy metabolism in the eucaryote system Central Asia organelle is unusual important function.The vacuole atp synthase participates in the ATP that keeps enough levels in the vacuole.Therefore, the vacuole atp synthase can be the target of the inhibition of double chain RNA mediate.

From the nucleotide sequence of the following albumen of CRW acquisition coding, described albumen shows the similitude with 40kDa V-ATPase.The amino acid sequence translation of SEQ ID NO:32 shows the autoploidy with Manduca sexta 40-kDa V-ATPase subunit amino acid sequence (GenBank numbers X98825).SEQ ID NO:33 and SEQ ID NO:34 correspond respectively to forward and reverse genome amplification primer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding 40kDa V-ATPase all or part of.But, use nucleotide sequence and the cDNA sequence that be in the news SEQ ID NO:32 shown in and inconsistent of crw genomic dna as the amplicon of template acquisition.

SEQ ID NO:33 and SEQ ID NO:34 represent the primer of heat amplification.Every primer all contains the T7 promoter sequence of 23 nucleotide, respectively at 1-23 position nucleotide.24-40 position nucleotide correspondence shown in the SEQ ID NO:33 is in the 95-111 position nucleotide shown in the SEQ ID NO:32.The reverse complementary sequence of the 24-43 position nucleotide correspondence sequence shown in the nucleotide of 362-381 position in SEQ ID:32 shown in the SEQ ID NO:34.In with the amplified reaction of crw genomic dna as template, use the primer of forming by SEQ IDNO:33 and SEQ ID NO:34 right, produced the amplicon of 291 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:35.Based on Martinez/Needleman-Wunsch DNA comparison, 268 nucleotide of the 24th nucleotide to the have only shown about 50% autoploidy with the nucleotide sequence shown in the SEQ ID NO:32 among the SEQ ID NO:35.Amplicon sequence and the sequence that be in the news SEQ ID NO:32 shown in and inconsistent of the hot amplimer that use is selected for use to obtaining.Preferably, use the cDNA of CRW mRNA storehouse or class libraries acquisition from then on to make amplicon.

Make following amplicon, described amplicon shows corresponding to the sequence of about the 95th nucleotide among the SEQ ID NO:32 to about the 381st nucleotide, it is cloned into plasmid vector, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 85th nucleotide among the SEQ ID NO:32 at least the sequence shown in about the 381st nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:32), reverse complemental RNA segment, or antisense strand is about the 381st nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 95th nucleotide at least among the SEQ ID NO:32, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:32.

EF1 α homologous sequence

It is very important for metabolism to transcribe extension and transcription factor, and they can be the favo(u)rable targets that is used for the inhibition of double chain RNA mediate.

Identified at least two CRW cDNA sequences and be used for the present invention, their quilts and the homologue that once was the energy code extension factor 1 alpha (EF1 α).

The amino acid translation of the singlet CRW cDNA sequence as shown in SEQ ID NO:36 has shown the autoploidy with Drosophila melanogaster EF-1-alpha amino acid sequence (GenBank numbers X06870).Also from CRW cDNA midgut library, identified other sequence that is predicted to be coding EF1 α homologous protein.Compare these sequences, produce the UNIGENE sequence, shown in SEQ ID NO:40, it is predicted to be and can be coded in the EF1 α albumen homology thing that is called as 48D herein.Some of the sequence that comprises in this singlet are predicted to be the following amino acid sequence of encoding, described amino acid sequence shows the autoploidy with multiple EF1 α homologous protein sequence, it includes but not limited to, Bombyx mori EF1 α (GenBank numbers D13338), Alternia species EF1 α (GenBank numbers X03704), Spragueia leo EF1 α (GenBank numbers U85680), ApismelliferaEF1 α (GenBank numbers AF015267), Anisakis simplex EF1 α (GenBank numbers AJ250539), Papaipema species EF1 α (GenBank numbers AF151628), Ephedrus persicae EF1 α (GenBank numbers Z83663), Papilio garamasEF1 α (GenBank numbers AF044833), Alysia lucicola EF1 α (GenBank numbers Z83667), Braco species EF1 α (GenBank numbers Z83669), Histeromerus mystacinus EF1 α (GenBank numbers Z83666) and Caenorhabditis elegans EF1 α (GenBank numbers U41534).

A CRW cDNA sequence that is predicted to be the part of coding EF1 α homologue is called as the B2 sequence in this article, and it is showed among the SEQ ID NO:36.SEQ ID NO:37 and SEQ ID NO:38 correspond respectively to forward and reverse genome amplification primer (is that primer is right, with reference to the corresponding or reverse complementary sequence shown in the SEQ ID NO:36), described primer is used for from crw genomic dna, from CRW mRNA storehouse or the cDNA that produces from class libraries thus make amplicon.The sequence of this type of amplicon is all or part of corresponding to the CRW gene of coding EF1 α homologous protein.But, when the cDNA sequence of the nucleotide sequence of the amplicon that obtains during as template with crw genomic dna and the report shown in the SEQ ID NO:36 and inconsistent.

SEQ ID NO:37 and SEQ ID NO:38 representative are used for the sequence of hot amplimer.They each all contain the T7 promoter sequence of 23 nucleotide, respectively at 1-23 position nucleotide.24-44 position nucleotide correspondence shown in the SEQ ID NO:37 is in the 8-29 position nucleotide shown in the SEQ ID NO:36.The reverse complementary sequence of the 24-42 position nucleotide correspondence sequence shown in the nucleotide of 310-328 position in SEQ ID:36 shown in the SEQ ID NO:38.In with the amplified reaction of crw genomic dna as template, use the primer of forming by SEQ IDNO:37 and SEQ ID NO:38 right, produced the amplicon of 933 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:39.328 nucleotide of the 8th nucleotide to the shown in nucleotide sequence shown in the SEQ ID NO:39 and the SEQ ID NO:36 are also inconsistent.Preferably, with the cDNA of CRW mRNA storehouse or class libraries acquisition from then on, for example, SEQ ID NO:36 makes amplicon.

Use CRW mRNA storehouse, or the cDNA of class libraries preparation from then on, make following amplicon, described amplicon shows corresponding to the sequence of about the 8th nucleotide among the SEQ ID NO:36 to about the 328th nucleotide, and it is cloned into plasmid vector.Reclaim the plasmid DNA of q.s, transcribe to allow carrying out external t7 rna polymerase from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 8th nucleotide among the SEQ ID NO:36 at least the sequence shown in about the 328th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ IDNO:36), reverse complemental RNA segment, or antisense strand is about the 328th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 8th nucleotide at least among the SEQ ID NO:36, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:36.

The primer that goes to be designed for the following crw genomic dna sequence of amplification with the sequence shown in the SEQ ID NO:40 is right, described sequential coding EF1 α 48D homologous protein sequence.SEQID NO:41 and SEQ ID NO:42 be corresponding forward and cdna reverse group amplimer (that is, primer to) respectively.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:41 and SEQ ID NO:42, respectively at 1-23 position nucleotide.24-41 position nucleotide correspondence shown in the SEQ ID NO:41 is in the 61-79 position nucleotide shown in the SEQ ID NO:40.The reverse complementary sequence of the 24-45 position nucleotide correspondence sequence shown in the nucleotide of 562-583 position in SEQ ID:40 shown in the SEQ ID NO:42.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:41 and SEQ IDNO:42 form, produced the amplicon of 569 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:43, its height is corresponding to the genomic part of CRW of the following albumen of coding, described albumen show with Drosophila melanogaster in the EF1 α albumen that also exists have the height homogeny.Corresponding to the nucleotide sequence shown in about 546 nucleotide among the SEQ ID NO:43 with the nucleotide sequence height shown in the about 61-583 position nucleotide shown in the SEQ ID NO:40 from about the 24th nucleotide.Do not observe sequence difference between the corresponding sequence in genome amplification subsequence and cDNA.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:43 is advanced plasmid vector.Reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:43 at least the sequence shown in about the 546th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:43), reverse complemental RNA segment, or antisense strand is about the 546th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:43, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:43.

26S proteosome subunit p28 homologous sequence

The 26S proteosome is big, dependency ATP, multimeric protein enzyme, and they are high conservative in all eucaryotes.It has general function in selectivity is removed the process of multiple short-lived albumen, described albumen was connected with the ubiquitin conjugation before this, was degraded by 26S protease complex then.The ubiquitin approach has important effect in the control of cell cycle, described control realizes by the specificity of multiple modulin is degraded, described albumen comprises the mitotic cell cyclin and to the kinase whose inhibitor of cyclin dependent, for example, the p27 of mammalian cell.Therefore, to the synthetic containment of 26S proteosome and to its form the selected objective target that subunit and degree containment can be the inhibition of double chain RNA mediate (Smith et al., PlantPhys.1997,113:281-291).

The cDNA sequence that obtains from CRW midgut library is accredited as and 26S proteosome subunit amino acid sequence homeologous, and it is used to the present invention.SEQ ID NO:44 is in fact corresponding to CRW midgut cDNA nucleotide sequence.The amino acid sequence translation of SEQ ID NO:44 has shown the autoploidy with 26S proteosome subunit p28 albumen (GenBank numbers AB009619).SEQ ID NO:45 and SEQ ID NO:46 correspond respectively to forward and reverse genome amplification primer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The amplicon that produces with this approach should show following sequence, the following CRW gene of described sequential coding all or part of, the homologue of described gene code 26S proteosome protein subunit.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:45 and SEQ ID NO:46, respectively at 1-23 position nucleotide.24-46 position nucleotide correspondence shown in the SEQ ID NO:45 is in the 130-152 position nucleotide shown in the SEQ ID NO:34.The reverse complementary sequence of the 24-41 position nucleotide correspondence sequence shown in the nucleotide of 423-440 position in SEQ ID:44 shown in the SEQ ID NO:46.In with the amplified reaction of crw genomic dna as template, use the primer of forming by SEQ ID NO:45 and SEQ ID NO:46 right, produced the amplicon of 1113 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:47.Sequence shown in sequence shown in the SEQ ID NO:47 and the SEQ IDNO:44 is also uncorrelated, therefore with the cDNA sequence that is in the news shown in the SEQ ID NO:44 and inconsistent.Preferably, use the cDNA of CRW mRNA storehouse or class libraries acquisition thus to make amplicon.

Manufacturing shows the amplicon of following sequence, and it is cloned into plasmid vector, described sequence corresponding to about the 130th nucleotide of SEQ ID NO:44 to about the 440th nucleotide, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 130th nucleotide among the SEQ ID NO:44 at least the sequence shown in about the 440th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:44), reverse complemental RNA segment, or antisense strand is about the 440th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 110th nucleotide at least among the SEQ ID NO:44, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:44.

Juvenile hormone EH albumen

Corpus allatum hormone is controlled the biological process of multiple necessity in the insect life cycle and is regulated and control, and described process is including but not limited to metamorphosis, breeding and diapause.In suitable, juvenile hormone (JH) concentration is required in harmful insect larva (particularly lepidoptera and coleoptera larva) form hemolymph and reaches peak value, and it must be degraded then, with the effect of middle finger hormone response.The enzyme that relates in the process of reduction juvenile hormone concentration plays a role by two main paties of metabolic degradation.Article one, approach relates to juvenile hormone esterase (JHE), and its energy hydrolysis methyl esters provides corresponding acid.Second kind of approach utilizes juvenile hormone EH (JHEH), to obtain the hydrolysis to epoxides, causes glycol to form.The contribution of JHE in the JH degraded understood well, finds that it is indeclinable between lepidoptera and coleoptera species.The inhibition of JH esterase and serious metamorphosis are changed relevant, include but not limited to, larva entanglement (larval wandering), pupate to postpone and the growth of lopsided intermediate state.On the contrary, people to the effect understanding of JHEH in the JH metabolism still less, and, it has demonstrated between species and can change, but recent research is at following evidence, described evidence hint JHEH may be main path (the Brandon J.Fetterolf of JH metabolism, Doctoral Dissertation, North Carolina State University (Feb.10,2002) Synthesis and Analysis of Mechanism Based Inhibitors of JuvenileHormone Epoxide Hydrolase from Insect Trichoplusia ni).At any time, contain that with gene technology can be to be used for the useful target that the pest of double chain RNA mediate suppresses to the interference of any JH degradation pathway.

The corpus allatum hormone EH sequence that obtains from CRW is identified, used it for the present invention.SEQ ID NO:48 is in fact corresponding to CRW midgut cDNA nucleotide sequence.The amino acid sequence translation of SEQ ID NO:48 predicted with Manduca sexta in the autoploidy of juvenile hormone EH (GenBank numbers U46682).SEQID NO:49 and SEQ ID NO:50 correspond respectively to forward and reverse amplimer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding JHEH homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:49 and SEQ ID NO:50, respectively at 1-23 position nucleotide.24-42 position nucleotide correspondence shown in the SEQ ID NO:49 is in the 7-26 position nucleotide shown in the SEQ ID NO:48.The reverse complementary sequence of the 24-44 position nucleotide correspondence sequence shown in the nucleotide of 360-380 position in SEQ ID:48 shown in the SEQ ID NO:50.In with the amplified reaction of crw genomic dna as template, use the primer of forming by SEQ ID NO:49 and SEQ ID NO:50 right, produced the amplicon of 95 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:52.The sequence of amplicon is not corresponding with the cDNA sequence shown in the SEQ ID NO:48.Preferably, use the cDNA of CRW mRNA storehouse or class libraries acquisition thus to make amplicon as the template nucleotide sequence in the amplified reaction.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:48 is advanced plasmid vector, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 7th nucleotide among the SEQ ID NO:48 at least the sequence shown in about the 380th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:48), reverse complemental RNA segment, or antisense strand is about the 380th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 7th nucleotide at least among the SEQ ID NO:48, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAseIII, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:48.

Rely on the chloride channel albumen homology sequence that expands

Relying on the chloride channel albumen that expands is assumed to be: play the part of pivotal player in eucaryon zooblast system osmotic adjustment.Therefore, the nucleotide sequence that shows the ability that can express following amino acid sequence can be to be used for carrying out the useful target that RNA suppresses pest, and described amino acid sequence is the autoploidy that shows the chloride channel albumen that expands with the dependence that identified in the past.

Infer the amino acid sequence homologous thing that relies on the chloride channel (SDCC) that expands from CRW cDNA library, use it for the present invention.SEQ ID NO:53 is in fact corresponding to CRW midgut cDNA nucleotide sequence.The amino acid sequence of SEQ ID NO:53 is confirmed as: with SDCC albumen (GenBank the numbers Y08484) homology among the zebra fish Danio rerio.SEQ ID NO:54 and SEQ ID NO:55 correspond respectively to forward and reverse hot amplimer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding SDCC homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:54 and SEQ ID NO:55, respectively at 1-23 position nucleotide.24-43 position nucleotide correspondence shown in the SEQ ID NO:54 is in the 78-97 position nucleotide shown in the SEQ ID NO:53.The reverse complementary sequence of the 24-41 position nucleotide correspondence sequence shown in the nucleotide of 332-349 position in SEQ ID:53 shown in the SEQ ID NO:55.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:54 and SEQ ID NO:55 form, produced the amplicon of 318 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:56, its genomic part of CRW with the following albumen of coding is highly corresponding, and described albumen has shown the height homogeny with SDCC albumen.Among the SEQ ID NO:56 among the nucleotide sequence of about the 24th nucleotide shown in about the 295th nucleotide and the SEQ IDNO:53 nucleotide sequence height shown in the nucleotide of 78-349 position corresponding.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:56 is advanced plasmid vector, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:56 at least the sequence shown in about the 295th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:56), reverse complemental RNA segment, or antisense strand is about the 295th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:56, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:56.

Robison ester 1-apodehydrogenase homologous sequence

Robison ester 1-apodehydrogenase (G6PD) catalysis Robison ester follows the oxidised form with nicotinamide adenine dinucleotide phosphoric acid (NADP+) to be reduced to NADPH to 6-phosphoglucose acid esters simultaneously.NADPH is as known in the art as the essential co-factor in a variety of eucaryote synthetic reactions, and it is its reduction form that known its can keep glutathione.The glutathione that is reduced plays a role as the street cleaner of dangerous oxidative metabolism product in eucaryote, and, under the assistance of glutathione peroxidase, change harmful hydrogen peroxide into water (Beutler et al, 1991, N.Engl.J.Med.324:169-174).Therefore, G6PD can be the selected objective target of the inhibition in no vertebra pest of double chain RNA mediate.

Infer the homologous amino acid sequence of Robison ester 1-apodehydrogenase (G6PD) from CRW cDNA library, use it for the present invention.SEQ ID NO:57 is in fact corresponding to CRW midgut cDNA nucleotide sequence.The amino acid sequence of SEQ ID NO:57 is confirmed as: show with bar fin fish species in the autoploidy of G6PD albumen (GenBank numbers U72484).SEQ ID NO:58 and SEQ ID NO:59 correspond respectively to forward and reverse genome amplification primer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding G6PD homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:58 and SEQ ID NO:59, respectively at 1-23 position nucleotide.24-46 position nucleotide correspondence shown in the SEQ ID NO:58 is in the 113-136 position nucleotide shown in the SEQ ID NO:57.The reverse complementary sequence of the 24-45 position nucleotide correspondence sequence shown in the nucleotide of 373-394 position in SEQ ID:57 shown in the SEQ ID NO:59.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:58 and SEQ IDNO:59 form, produced the amplicon of 328 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:60, its genomic part of CRW with the following albumen of coding is highly corresponding, and described albumen has shown the autoploidy with G6PD albumen.Among the SEQID NO:60 among the nucleotide sequence of about the 24th nucleotide shown in about the 305th nucleotide and the SEQ ID NO:57 nucleotide sequence height shown in the nucleotide of 113-394 position corresponding.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:60 is advanced plasmid vector, reclaim the plasmid DNA of q.s, transcribe to allow carrying out external t7 rna polymerase from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:60 at least the sequence shown in about the 305th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:60), reverse complemental RNA segment, or antisense strand is about the 305th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:60, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:60.

Actin 42A albumen homology sequence

Actin is an eukaryotic protein ubiquitous, high conservative, and it is cellular activity and motion needed (Lovato et al., 2001, Insect MoI.Biol.20:333-340).Identified a large amount of CRW cDNA sequences, they are predicted to be may encode actin or show the albumen of the amino acid sequence structure relevant with actin.Therefore, the gene of coding actin homologue can be the useful target of the inhibition of double chain RNA mediate in the pest cell.

One UNIGENE bunch (bunch 156_1) identifying in corn rootworm midgut cDNA library is made of many singlet est sequences, and wherein every all is predicted to be all or part of of actin homologous protein of encoding.These singlet are aligned to bunch, have obtained the consensus sequence shown in the SEQ IDNO:61, it is predicted to be the actin homologue of encoding.Homology actin sequence in the note group includes but not limited to Drosophila melanogaster actin 3 fragments, Helicoverpa armigera cell fibrinolysin (cytoplasmin) actin A3a (GenBank numbers X97614), Drosophila melanogaster actin (GenBank numbers X06383), hemichordata Saccoglossus kowalevskii actin mRNA sequence and Strongylocentrotus purpuratus actin (GenBank numbers X05739).

SEQ ID NO:62 and SEQ ID NO:63 correspond respectively to forward and reverse genome amplification primer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding actin homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:62 and SEQ ID NO:63, respectively at 1-23 position nucleotide.24-45 position nucleotide correspondence shown in the SEQ ID NO:62 is in the 14-35 position nucleotide shown in the SEQ ID NO:61.The reverse complementary sequence of the 24-45 position nucleotide correspondence sequence shown in the nucleotide of 449-470 position in SEQ ID:61 shown in the SEQ ID NO:63.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:62 and SEQ ID NO:63 form, produced the amplicon of 503 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:64, its genomic part of CRW with the following albumen of coding is highly corresponding, and described albumen has shown the autoploidy with actin.Among the SEQ ID NO:64 among the nucleotide sequence of about the 24th nucleotide shown in about the 480th nucleotide and the SEQ ID NO:61 nucleotide sequence height shown in the nucleotide of 14-470 position corresponding.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:64 is advanced plasmid vector, reclaim the plasmid DNA of q.s, transcribe to allow carrying out external t7 rna polymerase from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:64 at least the sequence shown in about the 480th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:64), reverse complemental RNA segment, or antisense strand is about the 480th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:64, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:64.

ADP-ribosylation factor 1 homologous sequence

ADP ribosylation factor 1 has been shown as in cell very important, because they embody complete effect in the process of dna damage reparation, carcinogenic, cell death and genome stability.Therefore, may in no vertebra pest species, optionally disturb transcribing of ADP-ribosylation factor with the inhibition of double chain RNA mediate.

Identified a large amount of CRW cDNA sequences, they are predicted to be: coding shows the amino acid sequence with the autoploidy of ADP-ribosylation factor.Especially, one UNIGENE bunch (bunch 88_1) is made of about 30 (30) bar EST singlet, and wherein every all is predicted to be all or part of of actin homologous protein of encoding.These singlet are aligned to bunch, have obtained the consensus sequence shown in the SEQ ID NO:65.The amino acid sequence translation that comprises the singlet CRW cDNA sequence of this bunch has been predicted following amino acid sequence, and described amino acid sequence shows the autoploidy with ADP-ribosylation factor homologue.The ADF-ribosylation factor protein sequence that shows the remarkable autoploidy of the amino acid sequence of inferring with ORF from SEQ ID NO:65 includes but not limited to Drosophila melanogaster ADP-ribosylation factor (GenBank numbers Y10618), Drosophilia obscura ADP-ribosylation factor (GenBank numbers AF025798), Anopheles gambiae ADP-ribosylation factor (GenBank numbers L11617) and Australian sheep calliphorid (Lycilia cuprina) ADP-ribosylation factor (GenBank numbers AF218587).

SEQ ID NO:66 and SEQ ID NO:67 correspond respectively to forward and reverse amplimer (be primer to), and described primer is used for from crw genomic dna, make amplicon from the CRWmRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding ADP-ribosylation factor homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:66 and SEQ ID NO:67, respectively at 1-23 position nucleotide.24-42 position nucleotide correspondence shown in the SEQ ID NO:66 is in the 70-88 position nucleotide shown in the SEQ ID NO:65.The reverse complementary sequence of the 24-40 position nucleotide correspondence sequence shown in the nucleotide of 352-368 position in SEQ ID:65 shown in the SEQ ID NO:67.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:66 and SEQ IDNO:67 form, produced the amplicon of 345 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:68, its genomic part of CRW with the following albumen of coding is highly corresponding, and described albumen has shown the autoploidy with the ADP-ribosylation factor protein.Among the SEQ ID NO:68 among the nucleotide sequence of about the 24th nucleotide shown in about the 322nd nucleotide and the SEQ ID NO:65 nucleotide sequence height shown in the nucleotide of 70-368 position corresponding.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:68 is advanced plasmid vector, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:68 at least the sequence shown in about the 322nd nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:68), reverse complemental RNA segment, or antisense strand is about the 322nd nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:68, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:68.

Transcription factor IIB albumen homology sequence

As mentioned before, transcribe extend and the translation termination factor extremely important for metabolism, can be the favo(u)rable target of the inhibition of double chain RNA mediate, be used to control or eliminate the invasion and attack of no vertebra pest.

Identified a kind of CRW cDNA sequence, it is predicted to be the following amino acid sequence of encoding, and described amino acid sequence has shown the autoploidy with transcription factor IIB albumen.SEQID NO:69 is used as and makes up the right basis of primer, and described primer is to being used to amplify the sequence of the following mRNA of coding from the CRW genome, and described mRNA has formed the basis at this cDNA sequence.

SEQ ID NO:70 and SEQ ID NO:71 correspond respectively to forward and reverse hot amplimer (be primer to), and described primer is used for from crw genomic dna, make amplicon from the CRWmRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of encoding transcription factor IIB homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:70 and SEQ ID NO:71, respectively at 1-23 position nucleotide.24-44 position nucleotide correspondence shown in the SEQ ID NO:70 is in the 4-24 position nucleotide shown in the SEQ ID NO:69.The reverse complementary sequence of the 24-44 position nucleotide correspondence sequence shown in the nucleotide of 409-429 position in SEQ ID:69 shown in the SEQ ID NO:71.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:70 and SEQ ID NO:71 form, produced the amplicon of 472 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:72, its genomic part of CRW with the following albumen of coding is highly corresponding, and described albumen has shown the autoploidy with transcription factor IIB albumen.Among the SEQID NO:72 among the nucleotide sequence of about the 24th nucleotide shown in about the 449th nucleotide and the SEQ ID NO:69 nucleotide sequence height shown in the nucleotide of 4-429 position corresponding.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:72 is advanced plasmid vector, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:72 at least the sequence shown in about the 449th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:72), reverse complemental RNA segment, or antisense strand is about the 449th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:72, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:72.

Chitinase protein

Chitin is β (1 → 4) homopolymer of N-acetylglucosamine, and it is found in the insect ectoskeleton.Chitin forms from the UDP-N-acetylglucosamine in the reaction of chitin synthase catalysis.Chitin is structural homopolysaccharide, in the structure to this hyperbranched and crosslinked structure, relates to a lot of enzyme steps.Chitin gives insect shape, rigidity and support, and the internal is provided, for example the support that adhered to of muscle.Chitin also should be degraded to a certain degree, with the step that relates in the regulation and control insect molting process.Therefore, it is believed that, double chain RNA mediate, to the inhibition of albumen in these approach, will can be used as the means that the no vertebra pest of control attacks.

From having identified amino acid sequence information to showing with the translation chitinase protein autoploidy, corn rootworm midgut cDNA library sequence.From alignment, produced a chitinase consensus sequence (UNIGENE bunch of number 716_1 to two singlet est sequences; SEQ IDNO:73).From alignment, produced second kind of chitinase consensus sequence (UNIGENE bunch of number 1238_1 to four singlet sequences; SEQ ID NO:77).The amino acid sequence translation that obtains from the ORF of these UNIGENE is noted as: horseradish ape chrysomelid (mustardbeetle) (Phaedon cochleariae) chitinase amino acid sequence (GenBank numbers Y18011).SEQ ID NO:73 and SEQ ID NO:77 are used as and make up the right basis of primer, are used for the genome from CRW, from CRW mRNA storehouse, or the cDNA sequence amplification two sequences from obtaining by this class mRNA storehouse.The nucleotide sequence of this type of amplicon should be corresponding to the gene of chitinase encoding homologous protein all or part of.

SEQ ID NO:74 and SEQ ID NO:75 correspond respectively to forward and reverse hot amplimer (be primer to), and described primer is used for from crw genomic dna, make amplicon from the CRWmRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of the chitinase encoding homologous protein shown in SEQ ID NO:73 all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:74 and SEQ ID NO:75, respectively at 1-23 position nucleotide.24-42 position nucleotide correspondence shown in the SEQID NO:74 is in the 1-19 position nucleotide shown in the SEQ ID NO:73.The reverse complementary sequence of the 24-47 position nucleotide correspondence sequence shown in the nucleotide of 470-493 position in SEQ ID:73 shown in the SEQ ID NO:75.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:74 and SEQ ID NO:75 form, produced the amplicon of 472 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:76, its genomic part of CRW with the following albumen of coding is highly corresponding, and described albumen has shown the autoploidy with chitinase protein.Among the SEQ ID NO:76 among the nucleotide sequence of about the 24th nucleotide shown in about the 516th nucleotide and the SEQ ID NO:76 nucleotide sequence height shown in the nucleotide of 1-493 position corresponding.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:76 is advanced plasmid vector, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:76 at least the sequence shown in about the 516th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:76), reverse complemental RNA segment, or antisense strand is about the 516th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:76, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:76.

SEQ ID NO:78 and SEQ ID NO:79 correspond respectively to forward and reverse genome amplification primer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of the chitinase encoding homologous protein shown in SEQ ID NO:77 all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:78 and SEQ ID NO:79, respectively at 1-23 position nucleotide.24-44 position nucleotide correspondence shown in the SEQ ID NO:78 is in the 64-84 position nucleotide shown in the SEQ ID NO:77.The reverse complementary sequence of the 24-44 position nucleotide correspondence sequence shown in the nucleotide of 779-799 position in SEQ ID:77 shown in the SEQ ID NO:79.In with the amplified reaction of crw genomic dna as template, use the primer of forming by SEQ IDNO:78 and SEQ ID NO:79 right, produced the amplicon of 912 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:80.The comparison of cDNA sequence shown in the SEQ ID NO:77 and amplicon sequence discloses, and has substantial difference between two sequences, and about 32% sequence homogeny is only arranged.Preferably, use primer right, for example the primer shown in the SEQ ID NO:78 box 79 is right, and mRNA or cDNA make amplicon as template, and is inconsistent to avoid this type of.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:77 is advanced plasmid vector, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 64th nucleotide among the SEQ ID NO:77 at least the sequence shown in about the 799th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:77), reverse complemental RNA segment, or antisense strand is about the 799th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 64th nucleotide at least among the SEQ ID NO:77, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:77.

The ubiquitin binding enzyme homologous sequence

The ubiquitin approach has important effect in the control of cell cycle, this is to realize that by the specificity of a large amount of modulins is degraded described albumen comprises the mitotic cell cyclin, or to the kinase whose inhibitor of cyclin dependent, for example, the p27 of mammalian cell.Therefore, the gene of coding ubiquitin and related component can be the selected objective target of the inhibition of double chain RNA mediate (Smith et al., Plant Phys.1997,113:281-29).The proteolysis approach that relies on ubiquitin is one of main path of the interior albumen selective destruction of pair cell in the eucaryote.Ubiquitin is regulated with the enzyme that combining of substrate is subjected to obviously to be the diversity arrangement.Proteoclastic target can be that step between the peptide is regulated and control by many subunits 26S proteasome degradation at the ubiquitinization of substrate and its also.The complexity of ubiquitin system has hinted its central role for albumen circulation in the eukaryotic regulation and control, and involves other albumen in the approach, comprises ubiquitin kinase, ubiquitin binding enzyme, uiquitin-protease ligase and 26S proteosome subunit component.Therefore, it is believed that the inhibition to this pathway protein of RNA mediation will can be used as the means of the no vertebra pest invasion and attack of control and use.

Identified following CRW cDNA library sequence, it is predicted to be the following amino acid sequence of encoding, and described amino acid sequence has shown the autoploidy with ubiquitin binding enzyme.SEQ IDNO:81 is used as and makes up the right basis of primer, and described primer is to being used to make amplicon, and described amplicon comprises all or part of from the ubiquitin binding enzyme of corn rootworm.

SEQ ID NO:82 and SEQ ID NO:83 correspond respectively to forward and reverse genome amplification primer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding ubiquitin binding enzyme homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:82 and SEQ ID NO:83, respectively at 1-23 position nucleotide.24-42 position nucleotide correspondence shown in the SEQ ID NO:82 is in the 16-34 position nucleotide shown in the SEQ ID NO:81.The reverse complementary sequence of the 24-42 position nucleotide correspondence sequence shown in the nucleotide of 295-313 position in SEQ ID:81 shown in the SEQ ID NO:83.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:82 and SEQ IDNO:83 form, produced the amplicon of 344 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:84, its genomic part of CRW with the following albumen of coding is highly corresponding, and described albumen has shown the autoploidy with ubiquitin binding enzyme.Among the SEQID NO:84 among the nucleotide sequence of about the 24th nucleotide shown in about the 321st nucleotide and the SEQ ID NO:81 nucleotide sequence height shown in the nucleotide of 16-313 position corresponding.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:84 is advanced plasmid vector, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:84 at least the sequence shown in about the 253rd nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:84), reverse complemental RNA segment, or antisense strand is about the 253rd nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:84, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:84.

The glyceraldehyde-3-phosphate dehydrogenase homologous sequence

The sugar decomposition approach is important approach very in most of biologies, and it relates to from degradation of glucose and produces metabolisable energy.In the second stage of sugar decomposition approach, an important enzyme is glyceraldehyde-3-phosphate dehydrogenase (G3PDH), and under the situation that has NAD+ and inorganic phosphate, the phase can be oxidized to glycerol 3-phosphate-phosphoric acid by the catalysis glyceraldehyde 3-phosphate, forms NADH thereupon.The important component of this reaction is that energy is by the formation storage of NADH.The encode gene of the enzyme relevant with the sugar decomposition approach, and especially, be coded in and have the gene that relates to the enzyme in the step that can be used for forming the energy reserve thing, can become the useful especially target of in no vertebra pest thing, carrying out the inhibition of double chain RNA mediate.

Identified following CRW cDNA library sequence, it is predicted to be the following amino acid sequence of encoding, and described amino acid sequence has shown the autoploidy with glyceraldehyde-3-phosphate dehydrogenase (G3PDH) albumen.From the overlap of three singlet est sequences assemble out shown in the SEQ ID NO:85 bunch consensus sequence.The amino acid sequence of ORF has shown with the G3PDH amino acid sequence (GenBank numbers AF126158) that obtains from Crytococcus curvatus G3PDH gene and from the autoploidy of the G3PDH Argine Monohydrochloride sequence (GenBank numbers AF025809) of Drosophila pseudoobscura among the nucleotide sequence SEQ ID NO:85.Therefore, the amino acid sequence translation of the sequence shown in the SEQ ID NO:85 is predicted to be the part of CRW G3PDH zymoprotein.Nucleotide sequence shown in the SEQ ID NO:85 is used as and makes up the right basis of hot amplimer, and described primer is to being used to make amplicon, the sequence of described amplicon coding CRW G3PDH enzyme sequence.

SEQ ID NO:86 and SEQ ID NO:87 correspond respectively to forward and reverse hot amplimer (be primer to), and described primer is used for from crw genomic dna, make amplicon from the CRWmRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding G3PDH homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:86 and SEQ ID NO:87, respectively at 1-23 position nucleotide.24-45 position nucleotide correspondence shown in the SEQ ID NO:86 is in the 103-124 position nucleotide shown in the SEQ ID NO:85.The reverse complementary sequence of the 24-45 position nucleotide correspondence sequence shown in the nucleotide of 573-594 position in SEQ ID:85 shown in the SEQ IDNO:87.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:86 and SEQ ID NO:87 form, produced the amplicon of 538 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:88, its genomic part of CRW with the following albumen of coding is highly corresponding, and described albumen has shown the autoploidy with ubiquitin binding enzyme.Among the SEQ ID NO:88 among the nucleotide sequence of about the 24th nucleotide shown in about the 515th nucleotide and the SEQ ID NO:85 nucleotide sequence height shown in the nucleotide of 103-594 position corresponding.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:88 is advanced plasmid vector, reclaim the plasmid DNA of q.s, transcribe to allow carrying out external t7 rna polymerase from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:88 at least the sequence shown in about the 515th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:88), reverse complemental RNA segment, or antisense strand is about the 515th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:84, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:88.

Ubiquitin B homologous sequence

As mentioned above, the ubiquitin protein degradation pathway has important effect in the control of cell cycle, this is to realize by the specificity of a large amount of modulins is degraded, described albumen comprises the mitotic cell cyclin, or to the kinase whose inhibitor of cyclin dependent, for example, the p27 of mammalian cell.Therefore, the gene of coding ubiquitin and related component can be the selected objective target that is used for the inhibition of double chain RNA mediate (Smith et al., Plant Phys.1997,113:281-291).

Identified following CRW cDNA library sequence, it is predicted to be the following amino acid sequence of encoding, and described amino acid sequence has shown the autoploidy with ubiquitin B albumen.Assemble out the consensus sequence of UNIGENE bunch shown in the SEQ ID NO:89 from the overlap of four singlet est sequences.The amino acid sequence translation of nucleotide sequence SEQ ID NO:89 shown with from the polymerization ubiquitin amino acid sequence (GenBank numbers AF034789) of Amoeba proteus with from the autoploidy of the ubiquitin protein sequence (GenBank numbers M22428) of Drosophila melanogaster.Therefore, the amino acid sequence translation of the sequence shown in the SEQ ID NO:89 is believed the ubiquitin B that can encode.SEQ ID NO:89 is used as and makes up the right basis of primer that is used for hot amplified reaction, and described primer is to being used for all or part of nucleotide sequence of amplification coding corn rootworm ubiquitin B amino acid sequence.

SEQ ID NO:90 and SEQ ID NO:91 correspond respectively to forward and reverse hot amplimer (be primer to), and described primer is used for from crw genomic dna, make amplicon from the CRWmRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding ubiquitin B homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:90 and SEQ ID NO:91, respectively at 1-23 position nucleotide.24-40 position nucleotide correspondence shown in the SEQ ID NO:90 is in the 62-78 position nucleotide shown in the SEQ ID NO:89.The reverse complementary sequence of the 24-47 position nucleotide correspondence sequence shown in the nucleotide of 399-422 position in SEQ ID:89 shown in the SEQ IDNO:91.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:90 and SEQ ID NO:91 form, produced the amplicon of 407 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:92, its genomic part of CRW with the following albumen of coding is highly corresponding, and described albumen has shown the autoploidy with ubiquitin binding enzyme.Among the SEQ ID NO:92 among the nucleotide sequence of about the 24th nucleotide shown in about the 384th nucleotide and the SEQ ID NO:89 nucleotide sequence height shown in the nucleotide of 62-422 position corresponding.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:92 is advanced plasmid vector, reclaim the plasmid DNA of q.s, to allow carrying out external T7 rna polymerase transcribe from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 24th nucleotide among the SEQ ID NO:92 at least the sequence shown in about the 384th nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:92), reverse complemental RNA segment, or antisense strand is about the 384th nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 24th nucleotide at least among the SEQ ID NO:92, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:92.

The juvenile hormone esterase homologue

As indicated above, corpus allatum hormone is controlled the biological process of multiple necessity in the insect life cycle and is regulated and control, and it includes but not limited to, metamorphosis, breeding and diapause.Use gene to contain the effective target of the pest control that technology interference synthetic to JH or degradation pathway may be a double chain RNA mediate.

The corpus allatum hormone esterase homologous sequence that obtains from CRW is identified, used it for the present invention.SEQ ID NO:93 height is corresponding to CRW midgut cDNA nucleotide sequence.The amino acid sequence translation of SEQ ID NO:93 has been predicted the autoploidy with juvenile hormone esterase (JHE).SEQ ID NO:94 and SEQ ID NO:95 correspond respectively to forward and reverse amplimer (be primer to), and described primer is used for from crw genomic dna, make amplicon from CRW mRNA storehouse or from the cDNA that class libraries thus produces.The sequence of this type of amplicon should be corresponding to the CRW gene of coding JHE homologous protein all or part of.Each contains the T7 promoter sequence of 23 nucleotide SEQ ID NO:94 and SEQ ID NO:95, respectively at 1-23 position nucleotide.24-45 position nucleotide correspondence shown in the SEQ ID NO:94 is in the 58-79 position nucleotide shown in the SEQ ID NO:93.The reverse complementary sequence of the 24-46 position nucleotide correspondence sequence shown in the nucleotide of 338-360 position in SEQ ID:93 shown in the SEQ IDNO:95.In with the amplified reaction of crw genomic dna as template, use is right by the primer that SEQ ID NO:94 and SEQ ID NO:95 form, the amplicon that has produced 348 base-pairs that comprise the nucleotide sequence shown in the SEQ ID NO:170 preferably, use CRW mRNA storehouse or from then on the cDNA that obtains of class libraries as the template nucleotide sequence in the amplified reaction.

The amplicons cloned that shows corresponding to the sequence of SEQ ID NO:170 is advanced plasmid vector, reclaim the plasmid DNA of q.s, transcribe to allow carrying out external t7 rna polymerase from the terminal arbitrarily embedding convergence T7 promotor of cloned sequence.Produce double-stranded RNA, sample is carried out biologic test; , a RNA segment, positive-sense strand, by about the 45th nucleotide among the SEQ ID NO:170 at least the sequence shown in about the 302nd nucleotide constitute that (difference is, there is the uracil residue in each position that is shown as thymidine in SEQ ID NO:96), reverse complemental RNA segment, or antisense strand is about the 302nd nucleotide essence reverse complementary sequence of the nucleotide sequence shown in about the 45th nucleotide at least among the SEQ ID NO:170, wherein, uracil suitably replaces thymidine.Remove to handle the sample of double-stranded RNA (dsRNA) with DICER or RNAse III, to produce the siRNA (siRNA) of q.s.The sample that will contain per 1,000,000 siRNA or dsRNA 0.15 part is used for previously described CRW meals biologic test, and larva was allowed to take food 13 days.Than contrast, the CRW larva that feed contains the meals of dsRNA has shown conspicuous growth inhibition and lethality, and described dsRNA is all or part of corresponding to the sequence shown in the SEQ ID NO:170.

Using from the parallel biologic test that the siRNA of double stranded rna molecule generation carries out, ten in the double stranded rna molecule listed above are checked.(its every kind all corresponding to following amino acid sequence with double-stranded RNA sequence sample or from the next siRNA sample of double-stranded RNA sequence sample preparation, described amino acid sequence is noted as selected target gene homologue, and they comprise: 40kDa V-ATPase homologue, the EF-1-alpha homologue, 26S proteosome subunit p28 homologue, juvenile hormone EH homologue, the CHD3 homologue, beta-tubulin homologue, two kinds of chitinase homologues, transcription factor IIB homologue and juvenile hormone esterase homologue (correspond respectively to SEQ ID NO:35, SEQ IDNO:39, SEQ ID NO:47, SEQ ID NO:52, SEQ ID NO:7, SEQID NO:21, SEQ ID NO:76, SEQ ID NO:80, SEQ ID NO:72 and SEQ ID NO:06)) be applied to insect meals (solution that 30 microlitres is contained the double-stranded RNA sample that is adjusted to suitable concn joins in the microtitre version hole of containing every hole 200 microlitre insect meals) with the concentration of about per 1,000,010 parts.Every kind of sample uses 18 holes altogether.The RNA sample diffusion is advanced after the meals, and single first instar larvae is only joined in each hole.As indicated above, biologic test was cultivated about 13 days, monitor M ﹠ M every day.Amino acid sequence variant Cry3Bb1 is killed the insect crystalline protein (at English et al. (U.S. Patent number 6,642,030) be named as insecticidal protein 11231 in) be used as positive control, be used to observe especially at the insect biologically active extremely that is harmful to corn rootworm.Described according to English etal., Cry3Bb is used for meals, difference is that the concentration of Cry3Bb is adjusted to per 1,000,000 200-300 parts in the meals.Only the independent control sample of handling with buffer solution or water is also comprised into test.The double-stranded RNA control sample and from the siRNA control sample that the double-stranded RNA control sample produces be used as extra recessiveness contrast included (

RNAi Kit, AMBION, Austin, Texas).

The initial evaluation and test that the double stranded rna molecule that use obtains from above-mentioned ten sequences carries out shows, the larva of the meals that contain following double-stranded RNA of being allowed to take food has shown significant lethality than contrast, and described double-stranded RNA is corresponding to 40kDa V-ATPase homologue (SEQID NO:35), CHD3 homologue (SEQ ID NO:7) and beta-tubulin homologue (SEQ ID NO:31).Based on such result, carry out extra biologic test, to check little interference double-stranded RNA particle whether more effective than total length double stranded rna molecule.

Alpha tubulin homologous sequence

Eukaryotic cells utilizes the cytoskeletal structure element usually, and they are not only important in as machinery mount, and are also important in the maintenance of pair cell shape.Half pliable and tough microfibril makes cell to move, and helps them to separate in mitosis (division of cytoplasm), and, in vertebrate and invertebrate, be used for contraction of muscle.Relatively harder microtubule is made of alpha and beta tubulin, and they have important effect in following process: a cover highway that rises as transhipment vesica and cell plays a role, and is used for separating chromosome during mitosis (nuclear division).Pliable and tough intermediate filament provides the extra at least intensity for whole cell result.Also known, cytoskeleton participates in passing cytoplasmic signal process.Consider these functions, we believe, any interference of pair cell skeleton or even all may cause the disease consequence of pair cell to the minor alteration of its integrality.

Identified at least a CRW cDNA library sequence, it is accredited as to encode and shows amino acid sequence with the autoploidy of following albumen, described albumen is called as the alpha tubulin in this article, more specifically, refers to the SEQ ID NO:163 shown in the sequence table in this article.The amino acid sequence translation of the sequence shown in SEQ ID NO:163 is believed can encode alpha tubulin or its fragment.SEQ ID NO:63 is used as the basis that makes up following sequence, and described sequence is predicted to be: be expressed among the E.coli or in plant the time, can be formed double-stranded RNA by the plant function promoter expression by T7.The sequence that is used as the basis that is used for this type of double-stranded RNA coded sequence is 1010 nucleotide of the 58th nucleotide to the of the SEQ ID NO:97 shown in the sequence table.This sequence can be used as the RNA developed by molecule, is purified, and tests in external feeding test, to measure the inhibition to corn rootworm.

T7 rna polymerase promoter is introduced in the upstream of the nucleotide sequence shown in 1010 nucleotide of the 58th nucleotide to the of SEQ ID NO:97, and (pIC17527) produces RNA from this construct.Adopt three parts of repeat samples, in external feeding test, this type of RNA is checked at corn rootworm, described check is carried out at beta tubulin positive control (mentioned above), 200ppm Cry3Bb and the contrast that is not subject to processing, and measures average mortality.The control sample that is not subject to processing has shown the lethality less than about 3-5%, and all other sample surveys have shown about 20 to about 55% lethality.The Cry3Bb sample has shown about 20 to about 36% lethality, and pIC17527 sample (15ppm) then shows about 38 to about 45% lethality.D8 (the beta tubulin the as mentioned) sample that is similarly about 15ppm shows about 38 to about 52% lethality.Based on these results, alpha tubulin construct is placed under the control of plant function promotor, is used for the maize transformation plant, at the ability of opposing corn rootworm invasion and attack, the transformation event that produces from described conversion is checked.

Be converted from the root of R0 milpa with the nucleotide sequence district shown in the SEQ ID NO:97.In brief, the sequence of coding dsRNA construct among the above-mentioned SEQ ID NO:97 at 5 ' end and link to each other by being operatively connected the sequence that constitutes in the e35S promotor of corn hsp70 intron, is held 3 ' to link to each other with poly-adenosine sequence with NOS3 ' tanscription termination.This expression cassette is positioned over the downstream that careless glycosides phosphine is selected box.Then these boxes that link to each other are placed into Agrobacterium tumefaciens Plant Transformation function carrier, new support is named as pMON72829 (alpha tubulin dsRNA construct), is used for the maize transformation tissue, makes it have careless glycosides phosphine tolerance, the selection incident shifts soil.The velamen of R0 plant is fed and is raised to western corn rootworm larva (WCR, Diabrotica virifera).With the MS0D medium that contains antibiotic and careless glycosides phosphine the transgenic corns root is transferred on the culture dish, carried out external selection.Make in each ware every root be subjected to the invasion and attack of two WCR larvas with thin head brush.Seal these wares with Parafilm, prevent the larva escape.Test is carried out under complete dark in 60% the RHPercival incubator at 27 ℃.Pollution and larva quality are monitored.After root tissue feed six days, larva is transferred in the WCR meals in 96 orifice plates.Larva be allowed to take food this meals eight days make that total test is that fortnight is long.To the larva quality and the in addition record of surviving, be used for analyzing.A kind of analysis is carried out on larva qualitative data and Dunnett ' s check basis, is used for seeking the significance,statistical that compares with LH244 (unconverted negative control).The WCR larva is two kinds of incidents on the feed, after ZM_S125922 and the ZM_S125938, than the growth of the larva of feed negative control plant, obviously hypoevolutism (α=0.05) (p＜0.02).The larva of feed negative control plant has shown about 0.6 to about 0.8mg average larva quality, and the larva of feed transgenosis root has then shown about 0.1 to about 0.2mg average larva quality.

After reaching suitable size, the transfer-gen plant (R0) that uses pMON72829 to produce is planted in 10 inches bottles that contain Metromix soil.When plant reaches the V4 vegetative stage, make about 1000 Western corn rootworms (WCR, Diabrotica virifera) ovum attack into root area.Same genotypic non-transgenic corn is attacked at similar vegetative stage, to be used as negative control.Ovum is carried out preincubate, make and in 24 hours of invasion and attack, to hatch.Larva was allowed in root system system 3 weeks of feed.Remove plant from soil, it is cleaned, make and to be evaluated and tested root at the larva feed.Use Node InjuryScale (NIS) in addition classification of root damage, wherein 0, not damage of expression, a joint of 1 expression root has been lacked in 1.5 inches, and 2 expressions, two joints are short, and 3 expressions, 3 joints are short.Because the plant that is used to evaluate and test be transform after directly from tissue culture, also because transformation event is unique,, can not obtain statistics so only evaluate and test the individual plant plant at every kind of incident this moment.All plant in the test have all shown the sign of larva feed, and this shows and has obtained successful invasion and attack.Negative control plant root presents moderate to major injury, and average out to about 1.9 on the Node InjuryScale.To being checked from the individual plants of eight kinds of different transgenic events.The root of three strains provides the outstanding control to the larva feed in these genetically modified plants, and Node Injury Scale is average about 0.2 or littler.Root from two strains in the genetically modified plants has shown moderate feed damage, and other transgenosis five of three strains does not show the control to the larva feed.These data show, are expressed in the genetically modified plants and this plant when being provided in the corn rootworm meals, and the double chain nucleotide sequence that coding can form the RNA sequence of dsRNA can provide the protection at the invasion and attack of corn rootworm pest fully.

About other effect that lacks consistent observable lethality or select the sequence (comprising EF1alpha, 26S proteosome subunit and multiple other cDNA sequence) of carrying out the gene containment for use, a kind of explanation may be, for these genes, what express is the homologue that exists in the gene group of the following albumen of coding, described albumen has similar function, but show enough big sequence difference, make and use when selecting these sequences of containing that the RNAi approach can not play a role and contain homologue.

Embodiment 2

Present embodiment has been described significant pest and has been suppressed, and this is to raise the meals that contain from the double-stranded RNA sequence of this pest acquisition and realize by feeding to no vertebra pest.

By using, prepare the artificial meals that are enough to raise the corn rootworm larva from the sample of the double-stranded RNA sequence of six kinds of different corn rootworm cDNA library sequences acquisitions.The corn rootworm larva is by the fair feed meals a few days, than the corn rootworm of the control diet that only is allowed to take food, lethality, the incidence of disease and hypoevolutism monitored.The nucleotide sequence that is used for meals is to obtain from the sequence shown in SEQ ID NO:35, SEQ ID NO:29, SEQ ID NO:47, SEQ IDNO:52, SEQ ID NO:7 and the SEQ ID NO:31, they every kind corresponding to the nucleotide sequence that obtains from corn rootworm cDNA library, their deduction amino acid sequence translation corresponds respectively to and is noted as 40kDa V-ATPase homologue, EF1 α homologue, 26S proteosome subunit homologue, juvenile hormone epoxide hydroxylase enzyme homologue, CHD3 homologue and 'beta '-tubulin homologue.

According to mentioned above, produce double-stranded RNA corresponding to these sequences.Produce siRNA by using RNAse III enzyme that the dsRNA of correspondence is cut, known this enzyme can be cut into dsRNA the dsRNA fragment of 12-15bp, and described fragment contains 3 ' suspension and 5 ' phosphoric acid and 3 ' C-terminal of 2-3 nucleotide.The siRNA of Chan Shenging shows and the identical character of siRNA of using Dicer enzyme (related in the eucaryotic RNA i approach) generation with technical ability by this way.

According to mentioned above, dsRNA and siRNA are gone up sample in the CRW meals with about 0.15ppm.According to mentioned above,, 12 single corn rootworm larva is checked assessment result after 13 days separately at every kind of dsRNA or siRNA sample.

Than the contrast that is not subject to processing (UTC), feed contains the remarkable reduction (p＜0.05) of having observed the larva quality in the larva of meals of the following dsRNA sequence of 0.15ppm, and described dsRNA sequence is shown in SEQ ID NO:35, SEQ ID NO:52, SEQ ID NO:7 and the SEQ ID NO:31.The remarkable reduction (p＜0.05) of larva quality also is provided corresponding to the siRNA of the sequence of SEQ ID NO:35, SEQ ID NO:39, SEQ ID NO:47 and SEQ ID NO:7.But, is the larva sample size but is not enough to determine to set up: cause the larva quality the result of change at random than dsRNA or the siRNA that contrast at utmost reduces actually? or clear and definite result to the inhibition of some biological functions in the rootworm larva based on double chain RNA mediate? therefore, record a demerit based on these, with bigger larva sample size, the RNA sequence corresponding to SEQ ID NO:35, SEQ ID NO:39, SEQ ID NO:7 and SEQ ID NO:31 is evaluated and tested again.

At each of four kinds of RNA sequences in the evaluation and test, with dsRNA or siRNA sample application in each of 72 holes.Arrive the meals surface and allow sample to immerse and permission meals dry tack free by the 30 microlitre volume applications that will contain RNA, according to mentioned above, the dsRNA of sample 0.15ppm or siRNA on each hole.Single larva is joined in each hole, cultivated 13 days.The evaluation and test larval mortality and the incidence of disease, the quality of mensuration survival larva.Biologic test the results are shown in the table 1.

Table 1. biologic test result

All siRNA samples all are every hole 0.15ppm

UTC-10mM?TrisHCl?pH7.5

The STE-standard error

In the dsRNA biologic test, 1-phage dsRNA, EPICENTERTECHNOLOGIES, Madison, Wisconsin; In the siRNA biologic test,

RNAi Kit, AMBION, Austin, Texas

The 2-Cry3Bb variant is 300ppm in the dsRNA biologic test, is 200ppm in the siRNA biologic test.

Use Tukey ' s HSD method, all samples is compared mutually, but not only compare with any single contrast.It is slow that every kind of dsRNA that is verified or siRNA have observed significant larvae development, and this is that average quality by the contrast that is not subject to processing than the survival larva reduces and judges.Even more important ground, double-chain small disturbance RNA sample have shown the lethality that causes certain level and the ability of the incidence of disease (based on the larva quality that reduces), and this level is the same effective with positive control sample Cry3Bb variant 11231 at least.The above results shows, any double stranded rna molecule that the mRNA sequence that exists from the corn rootworm cell obtains when offering corn rootworm in the meals of corn rootworm, all is effective in and suppresses the invasion and attack of harmful corn rootworm to plant species.

Embodiment 3

Present embodiment has been described and be used for the nucleotide sequence of expressing at plant cell and the effect that this type of nucleotide sequence is provided in the corn rootworm meals.

Remove to make up the nucleotide sequence of coding with the CHD3 coded sequence that obtains from corn rootworm cDNA library through stable double-stranded RNA.It is right that coding CHD3 amino acid sequence directly is used to make up primer to a cDNA sequence homologue or a homologue part, shown in the SEQ ID NO:171, and described primer wherein uses corn rootworm genomic templates DNA to being used for hot amplified reaction.Primer shown in SEQ ID NO:5 and the SEQ ID NO:6 is to energy amplifying doulbe-chain genome amplification, and wherein a chain shows the sequence shown in the SEQ ID NO:7.Produce three nucleotide sequence segments from the nucleotide sequence shown in the SEQID NO:7.Use the nucleotide sequence shown in the SEQID NO:7 as template, right with the hot amplimer that shows the sequence shown in SEQ ID NO:8 and the SEQ ID NO:9 in hot amplified reaction, produced article one nucleotide fragment (SEQ ID NO:174).Use the nucleotide sequence shown in the SEQ ID NO:7 as template, right with the hot amplimer that shows the sequence shown in SEQ ID NO:11 and the SEQ ID NO:12 in hot amplified reaction, produced second nucleotide fragment (SEQ ID NO:13).Use the nucleotide sequence shown in the SEQ ID NO:7 as template, right with the hot amplimer that shows the sequence shown in SEQ ID NO:14 and the SEQ IDNO:15 in hot amplified reaction, produced the 3rd nucleotide fragment (SEQID NO:16).Article one, 3 ' of one of sheet chain rupture end is complementary with the 3 ' end of one of second sheet chain rupture, thereby in containing the hot amplified reaction of these two segments, the hybridization of the end of these complementations divides other 3 ' end to carry out polymerase-mediated extension to allow two chains from them.3 ' end of another chain of second segment is complementary with the 3 ' end of one of the 3rd silver chain rupture, thereby in containing the hot amplified reaction of these two segments, the end hybridization of these complementations divides other 3 ' end to carry out polymerase-mediated extension to allow two chains from them.Containing all these segments and their complementary seriess, be in the hot amplified reaction of article one, second and the 3rd segment, with the hot amplimer sequence shown in SEQ ID NO:8 and the SEQ ID NO:15, produced the new sequence shown in SEQ ID NO:17, when this new sequence is positioned under the promotor control of working in the plant, can produce and the identical RNA nucleotide sequence of sequence height shown in the SEQ ID NO:17, just except existing the uracil residue to replace thymine residue.This RNA nucleotide sequence can utilize the reverse complemental of the 3rd segment and article one segment, form through stable RNA molecule, wherein, among the SEQ ID NO:17 corresponding to about the 303rd nucleotide of the 3rd segment to the part of about the 473rd nucleotide and the SEQ ID NO:17 corresponding to the part hybridization of about the 1st nucleotide of article one segment to about the 171st nucleotide, article one, links to each other with the open close second nucleotide sequence segment of crossing of the 3rd silver, in this embodiment, represent by about the 172nd nucleotide to the part of about the 302nd nucleotide corresponding to the second segment among the SEQ ID NO:17.Be listed in expression in the plant cell corresponding to the nucleotides sequence of SEQ ID NO:17 and cause synthetic through stable RNA molecule.The plant cell that the nucleotide sequence shown in the SEQ ID NO:17 can be transcribed into the RNA sequence can be provided in the meals of corn rootworm.As the synthetic repressed result of CHD3 homologous protein, the corn rootworm of this type of plant cell of taking food stops feed, grows for the beetle that grows up is hindered, and breeding is hindered, and is dead or suffer any or all of of these influences.

Remove to make up the nucleotide sequence of coding with the 'beta '-tubulin coded sequence that obtains from corn rootworm cDNA library through stable double-stranded RNA.It is right that the coding for beta-tubulin amino acid sequence directly is used to make up primer to a cDNA sequence homologue or a homologue part, shown in the SEQ ID NO:18, and described primer wherein uses corn rootworm genomic templates DNA to being used for hot amplified reaction.Primer shown in SEQ ID NO:19 and the SEQ ID NO:20 is to energy amplifying doulbe-chain genome amplification, and wherein a chain shows the sequence shown in the SEQ ID NO:21.Produce three nucleotide sequence segments from the nucleotide sequence shown in the SEQ ID NO:21.Use the nucleotide sequence shown in the SEQ ID NO:21 as template, right with the hot amplimer that shows the sequence shown in SEQ ID NO:22 and the SEQ ID NO:23 in hot amplified reaction, produced article one nucleotide fragment (SEQ ID NO:173).Use the nucleotide sequence shown in the SEQ ID NO:21 as template, right with the hot amplimer that shows the sequence shown in SEQ ID NO:25 and the SEQ ID NO:26 in hot amplified reaction, produced second nucleotide fragment (SEQ ID NO:27).Use the nucleotide sequence shown in the SEQ ID NO:21 as template, right with the hot amplimer that shows the sequence shown in SEQ IDNO:28 and the SEQ ID NO:29 in hot amplified reaction, produced the 3rd nucleotide fragment (SEQ ID NO:36).Article one, 3 ' of one of sheet chain rupture end is complementary with the 3 ' end of one of second sheet chain rupture, thereby in containing the hot amplified reaction of these two segments, the hybridization of the end of these complementations divides other 3 ' end to carry out polymerase-mediated extension to allow two chains from them.3 ' end of another chain of second segment is complementary with the 3 ' end of one of the 3rd silver chain rupture, thereby in containing the hot amplified reaction of these two segments, the end hybridization of these complementations divides other 3 ' end to carry out polymerase-mediated extension to allow two chains from them.Containing all these segments and their complementary seriess, be in the hot amplified reaction of article one, second and the 3rd segment, with the hot amplimer sequence shown in SEQ ID NO:22 and the SEQ ID NO:29, produced the new sequence shown in SEQ ID NO:31, when this new sequence is positioned under the promotor control of working in the plant, can produce the RNA nucleotide sequence identical, just except existing the uracil residue to replace thymine residue with the sequence height shown in the SEQ IDNO:31.This RNA nucleotide sequence can utilize the reverse complemental of the 3rd segment and article one segment, form through stable RNA molecule, wherein, among the SEQ ID NO:31 corresponding to about the 338th nucleotide of the 3rd segment to the part of about the 577th nucleotide and the SEQ ID NO:31 corresponding to the part hybridization of about the 31st nucleotide of article one segment to about the 250th nucleotide, article one, links to each other with the open close second nucleotide sequence segment of crossing of the 3rd silver, in this embodiment, represent by about the 251st nucleotide to the part of about the 337th nucleotide corresponding to the second segment among the SEQ IDNO:31.Be listed in expression in the plant cell corresponding to the nucleotides sequence of SEQ ID NO:31 and cause synthetic through stable RNA molecule.The plant cell that the nucleotide sequence shown in the SEQ ID NO:31 can be transcribed into the RNA sequence can be provided in the meals of corn rootworm.As the synthetic repressed result of 'beta '-tubulin, the corn rootworm of this type of plant cell of taking food stops feed, grows for the beetle that grows up is hindered, and breeding is hindered, and is dead or suffer any or all of of these influences.

Embodiment 4

Present embodiment has been described one or more compositions with insecticidal action and one or more synergies from the double-stranded RNA sequence of this no vertebra pest acquisition is provided in no vertebra pest meals, shown insecticidal effect when wherein, described one or more dsRNA sequences were provided in the pest meals in the past.

Shown in embodiment 3, the double stranded rna molecule that obtains from this pest is provided in the meals of no vertebra pest, cause inhibition to one or more biological functions in the pest, and act on the acquisition insecticidal effect thus, caused the death of pest, perhaps other feature that can be measured to, that reduced pest invasion and attack specific environment or host's ability.(every kind has nothing in common with each other mutually to add one or more other insecticides, every kind all obtains its insecticidal effect by obtaining the different mode of the mode of its insecticidal effect with dsRNA), can be so that the level that pest is controlled improves, and will further reduce: when use was piled the inhibition of pest with acquisition separately, pest may be developed the possibility that resistance to one or more insecticides or dsRNA.

For this is checked, make the CRW larva following meals of taking food, comprising the Cry3Bb rootworm Profilin of having advanced different content, and the double-stranded RNA of fixed amount, described RNA prepares described in embodiment 2 or 3, for example, corresponding to the dsRNA of SEQ ID NO:17 or SEQ ID NO:31.Observed the synergy that pest is suppressed.As shown in embodiment 2 and 3, the LD50 of Cry3Bb amount is used to obtain about 50% insect larvae lethality, and the companion of survival larva health degree reduces (judging than the minimizing of negative control by larva weight).Reduce the amount of insecticidal protein in the meals, cause the companion of lethality to reduce, and the increase of survival larva average weight.Adding all causes lethality almost completely corresponding to the dsRNA of SEQ ID NO:31 or SEQ ID NO:17 in the Cry3Bb of every kind of concentration, the average weight of any survival thing also significantly reduces.This has shown synergy.Concertedness may be to obtain by the interference to the larva midgut that the Cry3Bb that introduces any content (it is shown as: can introduce the hole in middle goldbeater's skin) causes.The hole can allow higher levels of double-stranded RNA kind to penetrate in the cell, perhaps even penetrate in the hemolymph, causes more efficiently the dsRNA kind being transported into larva, causes more efficiently reduction thus in the containment to target mRNA.The particular combinations that the hole forms composition and double-stranded RNA composition causes that increase and synergitic insecticidal action, because dsRNA more can disperse in hemolymph, cell and tissue away from the pest enteron aisle is exerted one's influence.Specific hole forms composition and includes but not limited to, insect toxicity albumen extremely (no matter whether they can show insect effect extremely to certain specific insect) from B.thuringiensis and the acquisition of relevant species, include but not limited to that further the hole of this toxoid forms domain.This type of hole forms composition can comprise that also one or more holes form toxin or its domain or its composition, they every kind all different, every kind all shows different binding modes, this is to judge by the passage formation attribute of every kind of toxin or domain, it comprises that dynamics, electricity that ion channel forms are led the size of attitude (conductance state), total membrane conductance, ion specificity and ion channel gate inhibition attribute.The combination that this type of hole forms composition and the dsRNA molecule that is specific to one or more genes of containment coleoptera species is by particularly including advancing this paper.

Embodiment 5

Present embodiment has been described the nucleotide sequence fragment of V-ATPase, when it is provided in the CRW species meals with the double-stranded RNA form, is useful on the control harmful insect.

Sequence shown in the SEQ ID NO:104 is the cDNA clone, 1870 nucleotide among the mRNA of 2400 nucleotide of the following albumen of its representative coding, described albumen shows the sequence homogeny with the height of Drosophila melanogaster vacuole ATPase (68kd, subunit 2).Use is checked order to this cDNA clone on two chains fully from the primer of initial sequence information design.These sequencing primers are listed as SEQ ID NO:105 to SEQID NO:120.SEQ ID NO:121 and SEQ ID NO:122 are primer sequences, are used for producing from the cDNA of cloning vector pSPORT (Invitrogen) copy of SEQ IDNO:104.Every primer contains the T7 promoter sequence of 20 nucleotide, and it is a 1-20 position nucleotide.The sequence of the cDNA flank that inserts in 21-44 position nucleotide among the SEQ ID NO:121 and the corresponding pSPORT carrier of the 21-45 position nucleotide among the SEQ IDNO:122.These primers allow the dna profiling that contains cDNA fragment (its arbitrary end, flank have the T7 promotor) is increased, and allow with the external generation double-stranded RNA of t7 rna polymerase.When the double-stranded RNA that will obtain from SEQ ID NO:104 comprise into the CRW meals, observe about 80% lethality.

By using following amplimer group, six zoness of different of SEQ ID NO:104 are checked: SEQ ID NO:123 and SEQ ID NO:124, its 1 to 291 nucleotide (being called as part #1,271 base-pairs) corresponding to SEQ IDNO:1; SEQID NO:125 and SEQ ID NO:126, it is corresponding to 292 to 548 nucleotide (being called as part #2,260 base-pairs); SEQ ID NO:127 and SEQ ID NO:128, it is corresponding to 549 to 830 nucleotide (being called as part #3,271 base-pairs); SEQID NO:129 and SEQ ID NO:130, it is corresponding to 840 to 1345 nucleotide (being called as part #4,505 base-pairs); SEQ ID NO:131 and SEQ ID NO:132, it is corresponding to 1360 to 1621 nucleotide (being called as part #5,261 base-pairs); SEQ ID NO:133 and SEQ ID NO:136, it is corresponding to 1540 to 1870 nucleotide (being called as part #6,278 base-pairs).Note part 5 and 6 overlapping about 80 base-pairs.When these 6 parts separately comprised in the CRW meals, #1, #2, #3 and #4 demonstrated the CRW lethality in 94% to 100% scope.Part #5 and #6 do not demonstrate and are higher than the above CRW lethality of visible background in the contrast that is not subject to processing.The sequence of part #1 representative is further divided into three littler parts, in these three littler parts each all by among the part #1 about at least 150 to about 180 continuous nucleotide representatives, thereby make among the part #1 that in first inferior part and part #1 overlap in second Asia, the 3rd inferior part overlapped with second Asia among the part #1.In the CRW biologic test, every kind in these inferior parts is tested respectively.Use this three kinds of shorter sequences, observed the lethality between 80% to 90%.

Second kind of means that the biologically active of the dsRNA molecule that obtains from the CRW gene is checked are the RNA molecules that make up self complementation.By identical DNA sequence and the combination of t7 rna polymerase promotor, can synthesize the single rna molecule of energy self complementation with inverted orientation.A kind of this type of RNA molecule is by 1 to 345 nucleotide and 50 to 325 nucleotide combinations in the nucleotide sequence shown in the SEQ ID NO:104 are obtained.The sequence that obtains is illustrated as SEQ ID NO:137, and it is named as pIC17527.PIC17527 is cloned into pTOPT2.1 (Invitrogen).Use the T7 promotor among the pTOP2.1, produced the dsRNA of about 500 base-pair nucleotide, it is comprised into CRW meals.The lethality that obtains is between 80% to 100%.

Embodiment 6

Present embodiment has been described the oral toxicity of dsRNA to Colorado potato bug (Leptinotarsadecemlineata).

(AmbionInc., Atustin TX), from Colorado potato bug (CPB), isolate total RNA among the Leptinotarsa decemlineata to use Ambion mirVana kit (catalog number (Cat.No.) 1560) and suggested design.For every kind of preparation, use the CPB larva that occupies about 200 μ L volumes in the micro-centrifuge tube.(CA), total RNA prepares cDNA with 5 micrograms for nvitrogen, Carlsbad to use Invitrogen Thermoscript RT-PCR system (catalog number (Cat.No.) 11146) and recommendation to be used for the synthetic scheme of random primer mediation cDNA.This cDNA is used as template, directly to the homologue sequence, wherein uses the TaqDNA polymerase and live alone as a widow nucleotide primer pr550 (SEQ ID NO:160) and pr552 (SEQ ID NO:161) with amplification V-ATPase A subunit 2.By comparison from the nearest V-ATPaseA of Manduca sexta (SEQ ID NO:151), Aedes aegypti (SEQ ID NO:152), Drosophila melanogaster (SEQ ID NO:153) and Diabrotica virgifera (WCR) directly to the autoploid nucleotide sequence, select the zone of minimum degeneracy, design above-mentioned primer.230-252 position nucleotide in the corresponding M.sexta gene order of primer pr550, and the 1354-1331 position nucleotide in the corresponding M.sexta gene order of primer pr552.

Use successively decrease (touchdown) amplification program obtain the amplification, wherein use following loop parameter:

94 ℃ of steps 1., 2 minutes;

94 ℃ of steps 2., 30 seconds;

50 ℃ of steps 3., 2 minutes;

72 ℃ of steps 4., 2 minutes

(step 2-4 carries out 35 circulations, and each circulation is decremented to-0.3 ℃ in the step 3)

72 ℃ of steps 5., 10 minutes; And

4 ℃ of steps 6..

The dna fragmentation of about 1.2kb that will obtain from cDNA amplification is cloned into carrier pCR2.1-TOPO (Invitrogen), to produce recombinant plasmid pIC17105.The nucleotide sequence (SEQ ID NO:144) that the clone inserts with from the Western corn rootworm, the V-ATPase A subunit 2 of Diabroticavirgifera is directly only shared 82% nucleotide sequence homogeny to the homologue sequence, but, but share 97% sequence homogeny about the deduction amino acid sequence of the V-ATPase A albumen that is encoded.

Use primer pr568 (SEQ ID NO:162) and pr569 (SEQ ID NO:163), amplify V-ATPase A among the plasmid pIC17105 directly to the homologue sequence, described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.The DNA that amplification obtains is used as template, and it is synthetic to be used for dsRNA, wherein uses Ambion MEGAscript ^TMKit (catalog number (Cat.No.) 1626) and suggested design (Ambion Inc., Austin, TX).In the insect feeding test, will directly feed the larva of raising to L.decemlineata from L.decemlineata V-ATPase A to the purified dsRNA that homologous sequence obtains.

The CPB meals are made of 13.2g/L agar (Serva 11393), 140.3g/L Bio-Serve premix (F9380B), 5ml/L KOH (18.3%w/w) and 1.25ml/L formalin (37%).Meals are disperseed on 96 orifice plates with the aliquot of 200 μ L, brief dry before application of samples.In each hole, use 20 μ L sample surveys, as the verification (check) that is not subject to processing (UTC) with aqua sterilisa.Order is dull and stereotyped dry before adding insect larvae.The CPB larva that in each hole, adds a new life with the fine, soft fur brush.With the described plate of sealable polyester film, ventilate with insect needle.Handle 40 larvas of check for every.At 27 ℃, 60% RH and complete dark are carried out 10-12 days cultivation to the biologic test plate down.To the slow and lethality of these dull and stereotyped record larvae development.Use

(N.C. USA) analyzes data for SASInstitute, Cary in 4 statistical softwares.

Table 2.dsRNA is to the oral toxicity of CPB larva

Based on the oral toxicity biologic test that uses CPB specificity V-ATPase dsRNA, can control the invasion and attack of CPB to plant by one or more following dsRNA sequences of expression are provided in the pest meals, described dsRNA sequence is specific to one or more genes of containment in the CPB pest.

Embodiment 7

Present embodiment has been described the result of the biologic test that on the artificial meals that use insect specificity dsRNA multiple lepidoptera larva is carried out.

Use Ambion mirVana kit (catalog number (Cat.No.) 1560) and suggested design (AmbionInc., Atustin, TX), isolate total RNA the third-instar larvae from second age to the of Spodoptera frugiperda, Helicoverpa zea, Agrotisipsilon and Ostrinia nubilalis.For every kind of preparation, use the larva that occupies about 200 μ L volumes in the micro-centrifuge tube.

Use Invitrogen Thermoscript RT-PCR system (catalog number (Cat.No.) 11146) and recommend to be used for the synthetic scheme (nvitrogen of random primer mediation cDNA, Carlsbad, CA), use from every kind the total RNA of 5 micrograms in the above-mentioned lepidoptera species and prepare cDNA.This cDNA is used as template, with amplifying specific in the V-ATPase of every kind of lepidoptera species A subunit 2 directly to the homologue sequence, wherein use Taq archaeal dna polymerase and live alone as a widow nucleotide primer pr550 (SEQ ID NO:160) and pr552 (SEQ ID NO:161).

By comparison from the nearest V-ATPase A of Manduca sexta, Aedes aegypti, Drosophilamelanogaster and Diabrotica virgifera (WCR) directly to the autoploid nucleotide sequence, select the zone of minimum degeneracy, design above-mentioned primer.230-252 position nucleotide in the corresponding M.sexta gene order of primer pr550, and the 1354-1331 position nucleotide in the corresponding M.sexta gene order of primer pr552.

The use PCR scheme of successively decreasing, and embodiment 6 described loop parameters obtain amplification.The DNA product cloning that amplification obtains is advanced pCR2.1-TOPO, check order to verify their homogeny.Contain directly and list in the table 3 to the recombinant plasmid of homologue gene order.

Table 3. lepidoptera V-ATPase A subunit 2 is directly to the homologue sequence

Use primer pr555 (SEQ ID:164) and pr556 (SEQ ID NO:156) to amplify V-ATPaseA among plasmid pIC17088, pIC17101, pIC17102, the pIC17102 directly to the homologue sequence, described primer is designed to: produce the dna fragmentation that flank oppositely has the T7 polymerase promoter, it is synthetic to be used for external dsRNA.

Use Ambion MEGAscriptTM kit (catalog number (Cat.No.) 1626) and suggested design (Ambion Inc., Austin, TX), the dna profiling that obtains from these amplifications synthesizes at FAW, BCW and CEW directly to the double-stranded RNA (dsRNA) of homologue sequence, and it is used for the insect biologic test with 10ppm.

At these tests, prepare artificial lepidoptera meals (165g/L SouthlandMultiple Species Diet, 14.48g/L agar), it is dispersed in 128 orifice plates each hole 500 μ l.Sample dispersion to meals, is positioned in " drying " chamber of 27 ℃ and 35% humidity, wherein, the excess water evaporation.In case be dried, just go to attack each hole, with the sealable polyester film bar sealing of perforation with single newborn larvae.27 ℃ of cultivations of described plate being carried out six to eight days.The insect that is not subject to processing was exhausting their whole meals in the hole separately in six to eight days.Prepare 50 orifice plates with the artificial meals of every hole 4ml, all insects that will meals promptly exhaust or almost exhaust before off-test are transferred in the new plate.Seal these plates, they are put back in the incubator,, again all biologic tests are evaluated and tested altogether after ten to 12 days.

Than the verification that is not subject to processing, aspect larval mortality or quality acquisition, do not demonstrate significant effect (use Tukey-Kramer HSD at all to comparing) from these results at the biologic test of lepidopterid species, adopt this test, observed growth (regimen).Form in the biologic test that the combination of BT insecticidal protein (before experiment in known toxic to above-mentioned lepidoptera pest) carries out in the hole of using dsRNA and sub-lethal dose, also do not observe the influence that larval mortality and quality are obtained.

Embodiment 8

Present embodiment has been described and has been used to measure dsRNA to boll weevil, the biologic test of the oral toxicity of Anthonomusgrandis.

(TX), from boll weevil (BWV), the larva of Anthonomus grandis is isolated total RNA for AmbionInc., Atustin to use Ambion mirVana kit (catalog number (Cat.No.) 1560) and suggested design.For every kind of preparation, use the BWV larva that occupies about 200 μ L volumes in the micro-centrifuge tube.(CA), total RNA prepares cDNA with 5 micrograms for nvitrogen, Carlsbad to use Invitrogen Thermoscript RT-PCR system (catalog number (Cat.No.) 11146) and recommendation to be used for the synthetic scheme of random primer mediation cDNA.This cDNA is used as template, directly to the homologue sequence, wherein uses the Taq archaeal dna polymerase and live alone as a widow nucleotide primer pr550 (SEQ ID NO:160) and pr552 (SEQ ID NO:161) with amplification V-ATPase A subunit 2.

By comparison from the nearest V-ATPase A of Manduca sexta, Aedes aegypti, Drosophilamelanogaster and Diabrotica virgifera (WCR) directly to the autoploid nucleotide sequence, select the zone of minimum degeneracy, design above-mentioned primer.230-252 position nucleotide in the corresponding M.sexta gene order of primer pr550, and the 1354-1331 position nucleotide in the corresponding M.sexta gene order of primer pr552.

The use PCR scheme of successively decreasing, and embodiment 6 described loop parameters obtain amplification.The dna fragmentation of about 1.2kb that will obtain from cDNA amplification is cloned into pCR2.1-TOPO (Invitrogen), to inserting order-checking, to verify.Use primer pr568 (SEQ ID:162) and pr569 (SEQ ID NO:163) to amplify V-ATPase A directly to homologue sequence (SEQ ID NO:149), described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.

(TX), the dna profiling that obtains from this amplification synthesizes double-stranded RNA (dsRNA) for Ambion Inc., Austin to use Ambion MEGAscriptTM kit (catalog number (Cat.No.) 1626) and suggested design.

For carrying out boll weevil, the biologic test of Anthonomus grandis Boheman according to manufacturers instruction, uses the artificial insect meals (Bioserv-F9247B based on agar; Gast and Davich, 1966).The thawing meals of about 200 μ l are disperseed into 96 hole titer plate, make its cooling curing.The sample (20 μ l) that will contain about 10ppm dsRNA then covers on the meals, makes its drying, and described dsRNA is corresponding to the identical sources thing sequence (SEQ ID NO:149) of V-ATPase A.Then the insect ovum (0-14) in 25 μ l, 0.1% agar is distributed on the meals.Use aperture seal bar (Zymark #72281) to go to seal titer plate then.At 27 ℃ ten to 12 days cultivation is carried out in test, accumulated by mensuration larva ight soil and assess activity.Do not observe influence, but this may be the physiological result of the specific feed of boll weevil to larval mortality or quality acquisition.In meals, dig a hole and significantly to have reduced the dosage of the dsRNA that absorbs, therefore significantly reduced the observed any effect of meeting when adopting surface feed physiology.In even mode dsRNA is comprised that the quality that mountain city into may obtain significant lethality and minimizing obtains.

Other target gene sequence from boll weevil can be cloned, and is used as template, is used for external synthetic dsRNA, can be checked dsRNA in the insect biologic test then, to evaluate their effect.For example, ribosomal protein L 19 (rpl19) gene can be used as and be used for the synthetic template of dsRNA.Purpose for the design degeneracy oligonucleotide primer, to from directly the comparing of Bombyx mori (SEQ ID NO:154), Drosophila melanogaster (SEQ ID NO:155), Anopholes gambiae (SEQ ID NO:156) and Diabrotica virgifera (SEQ ID NO:157), identify the total zone of minimum degeneracy to the nucleotide sequence of homologue at rpl19.Primer pr574 (SEQ ID NO:166) and pr577 (SEQ ID NO:168) or primer pr575 (SEQID NO:167) and pr577 (SEQ ID NO:168) can be used to amplify possible rpl19 directly to the homologue sequence from a variety of different insects species.

Use successively decrease the amplification scheme and as embodiment 6 described loop parameters obtain the amplification.The dna fragmentation of about 0.4kb that will obtain from boll weevil cDNA amplification is cloned into carrier pCR2.1-POTO (Invitrogen), to inserting order-checking, to verify.Use primer pr568 (SEQ ID:162) and pr569 (SEQ ID NO:163) to amplify rpl19 directly to homologue sequence (SEQ ID NO:149), described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.

Embodiment 9

Present embodiment has been described and has been used to measure dsRNA to red flour beetle, the biologic test of the oral toxicity of Triboliumcastaneum larva.

Some harmful insects are commercial particular importances, because they can be attacked from the agricultural product goods of specific crop production and through material processed.A kind of special this type of pest is a red flour beetle.Be specific to one or more dsRNA kinds that suppress one or more genes in this type of pest from the agricultural product goods of specific crop production and through existing the material processed, will be useful on these type of pest invasion and attack of control.

(TX), from red flour beetle (RFB), the larva of Tribolium castaneum is isolated total RNA for AmbionInc., Atustin to use Ambion mirVana kit (catalog number (Cat.No.) 1560) and suggested design.For every kind of preparation, use the RFB larva that occupies about 200 μ L volumes in the micro-centrifuge tube.(CA), total RNA prepares cDNA with 5 micrograms for nvitrogen, Carlsbad to use Invitrogen Thermoscript RT-PCR system (catalog number (Cat.No.) 11146) and recommendation to be used for the synthetic scheme of random primer mediation cDNA.This cDNA is used as template, directly to the homologue sequence, wherein uses the TaqDNA polymerase and live alone as a widow nucleotide primer pr550 (SEQ ID NO:160) and pr552 (SEQ ID NO:161) with amplification V-ATPase A subunit 2.

By comparison from the nearest V-ATPase A of Manduca sexta, Aedes aegypti, Drosophilamelanogaster and Diabrotica virgifera (WCR) directly to the autoploid nucleotide sequence, select the zone of minimum degeneracy, design above-mentioned primer.230-252 position nucleotide in the corresponding M.sexta gene order of primer pr550, and the 1354-1331 position nucleotide in the corresponding M.sexta gene order of primer pr552.

The use PCR scheme of successively decreasing, and embodiment 6 described loop parameters obtain amplification.The dna fragmentation of about 1.2kb that will obtain from cDNA amplification is cloned into pCR2.1-TOPO (Invitrogen), to inserting order-checking, to verify.Use primer pr568 (SEQ ID:162) and pr569 (SEQ ID NO:163) to amplify V-ATPase A directly to homologue sequence (SEQ ID NO:150), described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.

(TX), the dna profiling that obtains from this amplification synthesizes double-stranded RNA (dsRNA), uses it for the insect biologic test for Ambion Inc., Austin to use Ambion MEGAscriptTM kit (catalog number (Cat.No.) 1626) and suggested design.With wheat flour and water and corresponding to V-ATPase A directly to the dsRNA homogeneous mixture of homologue sequence (SEQ ID NO:150), make its drying, composition is used as the substrate of red flour beetle biologic test.After a couple of days cultivation, observe insect effect extremely by from flour/dsRNA mixture, extracting the weevil larva.

Other target gene sequence from red flour beetle can be cloned, and is used as template, is used for external synthetic dsRNA, can be checked dsRNA in the insect biologic test then, to evaluate their effect.For example, ribosomal protein L 19 (rpl19) gene can be used as and be used for the synthetic template of dsRNA.Purpose for the design degeneracy oligonucleotide primer, to from directly the comparing of Bombyx mori, Drosophila melanogaster, Anopholes gambiae and Diabrotica virgifera, identify the total zone of minimum degeneracy to the nucleotide sequence of homologue at rpl19.Primer pr574 (SEQ ID NO:166) and pr577 (SEQ ID NO:168) or primer pr575 (SEQ ID NO:167) and pr577 (SEQ ID NO:168) can be used to amplify possible rpl19 directly to the homologue sequence from a variety of different insects species.

Use successively decrease the amplification scheme and as embodiment 6 described loop parameters obtain the amplification.The dna fragmentation of about 0.4kb that will obtain from red flour beetle cDNA amplification is cloned into carrier pCR2.1-POTO (Invitrogen), to inserting order-checking, to verify.Use primer pr568 (SEQ ID:162) and pr569 (SEQ ID NO:163) to amplify rpl19 directly to homologue sequence (SEQ ID NO:159), described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.

Embodiment 10

Present embodiment has been described the biologic test of the oral toxicity that is used to measure dsRNA dialogue grub (white grub) and iron wire worm (wireworm).

(AmbionInc., Atustin TX), isolate total RNA from the larva of white grub or iron wire worm to use Ambion mirVana kit (catalog number (Cat.No.) 1560) and suggested design.For every kind of preparation, use the larva that occupies about 200 μ L volumes in the micro-centrifuge tube.(CA), total RNA prepares cDNA with 5 micrograms for nvitrogen, Carlsbad to use Invitrogen Thermoscript RT-PCR system (catalog number (Cat.No.) 11146) and recommendation to be used for the synthetic scheme of random primer mediation cDNA.This cDNA is used as template, directly to the homologue sequence, wherein uses the Taq archaeal dna polymerase and live alone as a widow nucleotide primer pr550 (SEQ ID NO:160) and pr552 (SEQ ID NO:161) with amplification V-ATPaseA subunit 2.

By comparison from the nearest V-ATPase A of Manduca sexta, Aedes aegypti, Drosophilamelanogaster and Diabrotica virgifera (WCR) directly to the autoploid nucleotide sequence, select the zone of minimum degeneracy, design above-mentioned primer.230-252 position nucleotide in the corresponding M.sexta gene order of primer pr550, and the 1354-1331 position nucleotide in the corresponding M.sexta gene order of primer pr552.

The use PCR scheme of successively decreasing, and embodiment 7 described loop parameters obtain amplification.The dna fragmentation of about 1.2kb that will obtain from cDNA amplification is cloned into pCR2.1-TOPO (Invitrogen), to inserting order-checking, to verify.Use primer pr568 (SEQ ID:162) and pr569 (SEQ ID NO:163) to amplify V-ATPase A directly to homologue sequence (SEQ ID NO:150), described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.

(TX), the dna profiling that obtains from this amplification synthesizes double-stranded RNA (dsRNA), uses it for the insect biologic test for Ambion Inc., Austin to use Ambion MEGAscriptTM kit (catalog number (Cat.No.) 1626) and suggested design.Behind a couple of days biologic test, observe the effect of oral toxicity.

Other target gene sequence of grub or iron wire worm of making clear one's meaning and position can be cloned, and is used as template, is used for external synthetic dsRNA, can be checked dsRNA in the insect biologic test then, to evaluate their effect.For example, ribosomal protein L 19 (rpl19) gene can be used as and be used for the synthetic template of dsRNA.Purpose for the design degeneracy oligonucleotide primer, to from directly the comparing of Bombyx mori, Drosophila melanogaster, Anopholes gambiae and Diabrotica virgifera, identify the total zone of minimum degeneracy to the nucleotide sequence of homologue at rpl19.Primer pr574 and pr577 or primer pr575 and pr577 can be used to amplify possible rpl19 directly to the homologue sequence from a variety of different insects species.

Use successively decrease the amplification scheme and as embodiment 7 described loop parameters obtain the amplification.The dna fragmentation of about 0.4kb that will obtain from red flour beetle cDNA amplification is cloned into carrier pCR2.1-POTO (Invitrogen), to inserting order-checking, to verify.Use primer pr568 (SEQ ID:162) and pr569 (SEQ ID NO:163) to amplify rpl19 directly to the homologue sequence, described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.

Embodiment 11

Present embodiment has been described and has been used to measure dsRNA to mosquito, the biologic test of the oral toxicity of Aedes aegypti.

(AmbionInc., Atustin TX), isolate total RNA from the larva of Aedes aegypti to use Ambion mirVana kit (catalog number (Cat.No.) 1560) and suggested design.For every kind of preparation, use the Aedes aegypti larva that occupies about 200 μ L volumes in the micro-centrifuge tube.(CA), total RNA prepares cDNA with 5 micrograms for nvitrogen, Carlsbad to use Invitrogen Thermoscript RT-PCR system (catalog number (Cat.No.) 11146) and recommendation to be used for the synthetic scheme of random primer mediation cDNA.This cDNA is used as template, directly to the homologue sequence, wherein uses the Taq archaeal dna polymerase and live alone as a widow nucleotide primer pr550 (SEQ ID NO:160) and pr552 (SEQ ID NO:161) with amplification V-ATPase A subunit 2.

By comparison from the nearest V-ATPase A of Manduca sexta, Aedes aegypti, Drosophilamelanogaster and Diabrotica virgifera (WCR) directly to the autoploid nucleotide sequence, select the zone of minimum degeneracy, design above-mentioned primer.230-252 position nucleotide in the corresponding M.sexta gene order of primer pr550, and the 1354-1331 position nucleotide in the corresponding M.sexta gene order of primer pr552.

The use PCR scheme of successively decreasing, and embodiment 7 described loop parameters obtain amplification.The dna fragmentation of about 1.2kb that will obtain from cDNA amplification is cloned into pCR2.1-TOPO (Invitrogen), to inserting order-checking, to verify.Use primer pr568 (SEQ ID:162) and pr569 (SEQ ID NO:163) to amplify V-ATPase A directly to homologue sequence (SEQ ID NO:150), described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.

(TX), the dna profiling that obtains from this amplification synthesizes double-stranded RNA (dsRNA), uses it for the insect biologic test for Ambion Inc., Austin to use Ambion MEGAscriptTM kit (catalog number (Cat.No.) 1626) and suggested design.Behind a couple of days biologic test, observe effect to insect larvae.

Other target gene sequence from mosquito can be cloned, and is used as template, is used for external synthetic dsRNA, can be checked dsRNA in the insect biologic test then, to evaluate their effect.For example, ribosomal protein L 19 (rpl19) gene can be used as and be used for the synthetic template of dsRNA.Purpose for the design degeneracy oligonucleotide primer, to from directly the comparing of Bombyxmori, Drosophila melanogaster, Anopholes gambiae and Diabroticavirgifera, identify the total zone of minimum degeneracy to the nucleotide sequence of homologue at rpl19.Primer pr574 and pr577 or primer pr575 and pr577 can be used to amplify possible rpl19 directly to the homologue sequence from a variety of different insects species.

Use successively decrease the amplification scheme and as embodiment 7 described loop parameters obtain the amplification.The dna fragmentation of about 0.4kb that will obtain from cDNA amplification is cloned into carrier pCR2.1-POTO (Invitrogen), to inserting order-checking, to verify.Use primer pr568 (SEQ ID:162) and pr569 (SEQ ID NO:163) to amplify rpl19 directly to the homologue sequence, described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.

(TX), the dna profiling that obtains from this amplification synthesizes double-stranded RNA (dsRNA), uses it for the insect biologic test for Ambion Inc., Austin to use Ambion MEGAscriptTM kit (catalog number (Cat.No.) 1626) and suggested design.

Other mosquito class species can be comprised scope into of the present invention.Can use suitable Oligonucleolide primers, the suitable target gene sequence from Aedes, Culex and Anopholes species is increased, it is cloned into carrier pCR2.1-POTO (Invitrogen), to inserting order-checking, to verify.Use primer pr568 (SEQ ID:162) and pr569 (SEQ IDNO:163) to amplify clone's target sequence, described primer is designed to " general " primer, is used for producing from pCR2.1-TOPO the dna profiling of the T7 polymerase promoter sequence with flank.

(TX), the dna profiling that obtains from these amplifications synthesizes double-stranded RNA (dsRNA), uses it for the insect biologic test for Ambion Inc., Austin to use Ambion MEGAscriptTM kit (catalog number (Cat.No.) 1626) and suggested design.

Embodiment 12

Present embodiment has been described: the dsRNA that makes from 3 ' the UTR zone of V-ATPase is what how to demonstrate the regulation and control of target.

The segment of WCR V-ATPase3 ' UTR (dsRNA of ca.300bp) has been used to carry out the WCR biologic test, but but fails to demonstrate in 12 days biologic test hypoevolutism and lethality.Sizable segment has but shown significant hypoevolutism and lethality in the V-ATPase coding region in the finite concentration scope.To raise total RNA that 4 days WCR larva of WCRV-ATPase 3 ' UTR segment extracts and carry out Northern marking hybridization (and go to survey with the coding region probe) demonstration from feeding: than the larva that is not subject to processing, V-ATPase target RNA significantly reduces (being summarised as NBP#7497215).But, stayed the signal that can be detected, this shows, comparatively invalid with 3 ' UTR dsRNA segment (than using the coding region segment) to knocking out of target, and/or from the contribution of second kind of possible V-ATPase gene, described second kind of gene has and first kind of visibly different 3 ' UTR of V-ATPase gene.Exist in Southern marking hybridization data that WCR is carried out and the genome to surpass the identical of views of a kind of hybrid gene sequence, but to the check of EST and there is the PCR of family of limitation not show that but possible second kind of gene transcribed.

Want important pointing out at this, larvae development potential target slow and that kill larva is crucial though determine to send as an envoy to, and by hybridization of the Northern marking or quantitative PCR the target that easy detection also can find to use the RNAi strategy is carried out in the expression of target gene.The above results adds that other Northern experiment that is conceived to the V-ATPase target shows that in insect, in a few hours that dsRNA exists, RNA is as can be seen for the influence of transcript abundance.

Embodiment 13

Present embodiment has been described a kind of method, is used to use the silencing methods of ta-siRNA mediation to carry out containment to the harmful insect gene.

Trans-acting siRNA (ta-siRNA) the class group (Dalmay et al., Cell 101:543-553,2000 that in the biology harmful, make the method for gene silencing use recent discovery to plant; Mourrain et al., Cell 101:533-542,2000; Peragine et al, Genesand Development, 18:2368-2379,2004; Vazquez et al, MoI Cell16 (l): 69-79,2004; Yu et al., Mol Plant Microbe Interact 16:206-216,2003).Ta-siRNA obtains from the single stranded RNA transcript of naturally occurring miRNA target.Use Microrna to be described in the U.S. Provisional Patent Application sequence number 60/643,136 (Carrington etal.2004) with the method for bringing out ta-siRNA and being used for carrying out gene silencing plant, its by reference integral body incorporate this paper into.Identified at least a pest specificity miRNA that in corn rootworm larva intestinal epithelial cell, expresses.Go to identify with this pest specificity miRNA then: at least a this sequence of target rna transcription, the miRNA complementation of expressing in described sequence and the cell.Corresponding target sequence is the short sequence that is no more than 21 continuous nucleotide, in cell type with functional r NAi approach, when a rna transcription part originally miRNA corresponding with it contacted, described short sequence caused the cutting to described transcript of silencer mediation.In case identified the miRNA target sequence, at least a miRNA target sequence and second sequence are merged, described second sequence is corresponding to using this method to carry out the part of reticent pest gene.For example, the sequence with miRNA target sequence and corn rootworm vacuole ATPase (V-ATPase) gene merges.The miRNA target sequence can be placed on 5 ' end of V-ATPase gene, and 3 ' holds or be embedded in the middle of this gene.Use is corresponding to the multiple miRNA target sequence of multiple miRNA gene, and it may be preferred perhaps repeatedly using with a kind of miRNA target sequence use in the chimera of miRNA target sequence and V-ATPase sequence.The V-ATPase sequence can be a random length, but minimum is 21bp.

Use a large amount of suitable promotors or any material in other transcriptional regulatory element, the chimera of miRNA target sequence and v-ATPase is expressed in the plant cell, at least can transcribe at the cell type that will be provided in the pest meals (for example, being used for controlling the corn root of corn rootworm) and get final product.

This method can have additional advantage: can be transported to the target pest than long RNA molecule.Typically, the dsRNA that produces in plant can be a short rna by the Dicer rapid processing, when beyond the source side formula feed when raising to some pests, this may be of no use.In the method, produce the strand transcript in plant cell, it is absorbed by pest, turns to dsRNA at the pest transit cell, in cell, it is processed into the ta-siRNA that can cause post-transcriptional silencing to one or more genes in one or more pests again.

Embodiment 14

Present embodiment has been described CRW cDNA sequence and comparison from the sequence in other source of non-CRW, and to the evaluation of the exclusive sequence of (1) sequence the same with the sequence in other source and (2) CRW.CDNA sequence conservative in two kinds of biologies is potential RNAi candidate sequence, and it can be used to the gene expression and the function of these two kinds of biologies of target.Perhaps, selecting the following sequence that is used for the containment of CRW gene may be people's needs, (a) other pest, (b) nontarget organism and (c) selectedly come not have the known homologous sequence of described sequence to exist with in the CRW containment sequence plant transformed genome.

Select six CRW cDNA sequences, be used for comparing in the sequence in other source.Specific sequence comprises the sequence of coding alpha-tubulin, beta-tubulin, CHD3, vacuolar proton pump E subunit, V-ATPase A subunit and silk-fibroin (thread protein).Nucleotide sequence is shown in respectively among SEQ ID NO:98, SEQ ID NO:99, SEQ IDNO:100, SEQ ID NO:101, SEQ ID NO:102, the SEQ ID NO:103.Use NCBI megablast program (Altschul et al., J.Mol.Biol.215:403-410,1990), CRW cDNA sequence is compared with all open cDNA from the multiple biology of GenBank, search parameter is as follows:

-W?21 -b50 -v50

The perfection coupling that this needs at least 21 bodies (21-mer) only keeps best 50 couplings and alignment.The result is filtered, only comprise belonging to Insecta OrderBiology, and honeybee (Apis mellifera) is left out.Though only analyze on six CRW cDNA sequences, same method can be used for cDNA all in CRW or other target organism or unigene sequence, and does not have undue burden and experiment.

Use six CRW cDNA sequences, from 20 kinds of different insect biologies, identified 145 kinds of couplings altogether.They comprise some pest species, for example, and acyrthosiphum pisim (Acyrthosiphon pisum), Asia oranges and tangerines wood louse (Diaphorina citri) and pediculus humanus capitis (Pediculus humanus).

These the results are shown in the following table 4, have wherein showed search sequence and have hit the insect species that sequence is hit in coupling, match-percentage homogeny and acquisition between the sequence.For example, identify, from the segment of the 844th to 1528 nucleotide among the SEQ ID NO:98 with identical from the segment height of the 812nd to 128 nucleotide among the GenBank sequence numbering GI:47521748 of acyrthosiphum pisim (Acyrthosiphon pisum).This two sequences is shared about 85% homogeny.

Embodiment 15

Present embodiment has been described: the coupling of the total model of use and known array and existing domain, and from the translation of nucleotide sequence disclosed herein being identified the protein function domain of prediction, and gene family.

At first use " translater " program to produce protein sequence, described program is translated as the titanium sequence with Unigene, and this is undertaken by following step: with the autoploidy of known protein; The gene structure that from the beginning starts prediction based on model; And the longest opening code-reading frame (ORF).Proofread and correct because the wrong position of frameing shift that causes of order-checking.Search for protein sequence (The Pfam Protein Families Database at Pfam database (covering the latent Markov model (HMM) of a lot of common protein families and the big collection of multiple sequence alignment) then, Bateman et al., Nucleic Acids Research 32:D138-D141,2004).Use default rigorous degree, with program HMMPAM (Durbin et al., Biological Sequence Analysis:Probabilistic Models of Proteins and Nucleic Acids, CambridgeUniversity Press, 1998) search for albumen HMM model.Further filter, only keep expected value and be 0.1 or littler those couplings as remarkable coupling.Article 20303, in the corn rootworm peptide sequence, 4199 (21%) bars have been identified with 1317 kinds of different protein structure domains and family.

Analysis result is showed in feature (feature) zone of sequence table file, has following characteristic: Pfam name, Pfam describe and with coupling level, expected value (E-value) and the peptide sequence of HMMPFAM mark in the quantity that copies of domain.

Embodiment 16

Present embodiment has been described a kind of method, is used to be provided for the dna sequence dna of the gene silencing of dsRNA mediation.More specifically, present embodiment has been described the selection to the improved DNA in the gene silencing that can be used for the dsRNA mediation, and this realizes by following step: (a) select initial dna sequence dna from target gene, it comprises the continuous nucleotide more than 21; (b) identify at least one shorter dna sequence dna, it constitutes by being predicted to be the zone that does not produce undesired polypeptide from the zone of initial dna sequence; And the dna sequence dna of (c) selecting the gene silencing that is used for the dsRNA mediation, it comprises at least one shorter dna sequence dna.Undesired polypeptide includes but not limited to, with the polypeptide of sensitization homologous peptide and with the polypeptide of known polypeptide toxin homology.

WCR V-ATPase shows: can play a role in the corn rootworm feeding test, with the silence (as the means of control larval growth) of check dsRNA mediation.CDNA sequence from the vacuole ATPase gene (V-ATPase) of Western corn rootworm (WCR) (Diabrotica cirgifera virgifera LeConte) is selected, and is used as initial dna sequence dna (SEQ ID NO:104).At following zone this initial dna sequence dna is screened, in described zone, the continuous fragment that each bar comprises at least 21 nucleotide only with known vertebrate sequence in 21 nucleotide that links to each other less than 21 couplings.Identified three segments that surpass about 100 continuous nucleotide, wherein do not contained above-mentioned 21/21 and hit; Article one, sequence fragment is corresponding to the 739-839 position nucleotide among the SEQ ID NO:104, the second sequence fragment is corresponding to the 849-987 position nucleotide among the SEQ ID NO:104, and the 3rd sequence fragment is corresponding to the 998-1166 position nucleotide among the SEQ ID NO:104.Make up this three sequences, make up gomphosis DNA array (SEQ ID NO:1), be used for mutually deserved CRW V-ATPase coded sequence is carried out the gene silencing of dsRNA mediation.In CRW biologic test mentioned above, the gomphosis DNA array of novelty is checked.

The open text of all that mention in this specification, patent and disclosed patent application all are merged in this paper by reference, this with state that especially, individually to incorporate every kind of independent open this paper or patent into this paper by reference the same.

Sequence table

<110>Monsanto?Technology?LLC

Baum，James?A

Gilbertson，Larry?A

Kovalic，David?K

LaRosa，Thomas?J

Lu，Maolong

Munyikwa，Tichifa?R.I.

Roberts，James?K

Wu，Wei

Zhang，Bei

＜120〉be used for composition and method at plant control insect infestations

<130>38-21(53597)

<150>60560842

<151>2004-04-09

<150>60565632

<151>2004-04-27

<150>60579062

<151>2004-06-11

<150>60603421

<151>2004-08-20

<150>60617261

<151>2004-10-11

<150>60669175

<151>2005-04-07

<160>174

<210>1

<211>409

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>1

<210>2

<211>157

<212>DNA

<213>Diabrotica?virgifera

<400>2

<210>3

<211>338

<212>DNA

<213>Diabrotica?virgifera

<400>3

<210>4

<211>458

<212>DNA

<213>Diabrotica?virgifera

<400>4

<210>5

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>5

<210>6

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>6

<210>7

<211>335

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>7

<210>8

<211>29

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>8

<210>9

<211>21

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>9

<210>10

<211>171

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>10

<210>11

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>11

<210>12

<211>32

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>12

<210>13

<211>112

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>13

<210>14

<211>24

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>14

<210>15

<211>30

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>15

<210>16

<211>245

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>16

<210>17

<211>473

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>17

<210>18

<211>536

<212>DNA

<213>Diabrotica?virgifera

<400>18

<210>19

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>19

<210>20

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>20

<210>21

<211>399

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>21

<210>22

<211>26

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>22

<210>23

<211>19

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>23

<210>24

<211>267

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>24

<210>25

<211>17

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>25

<210>26

<211>19

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>26

<210>27

<211>106

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>27

<210>28

<211>22

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>28

<210>29

<211>25

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>29

<210>30

<211>257

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>30

<210>31

<211>586

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>31

<210>32

<211>399

<212>DNA

<213>Diabrotica?virgifera

<400>32

<210>33

<211>40

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>33

<210>34

<211>43

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>34

<210>35

<211>291

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>35

<210>36

<211>451

<212>DNA

<213>Diabrotica?virgifera

<400>36

<210>37

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>37

<210>38

<211>42

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>38

<210>39

<211>933

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>39

<210>40

<211>918

<212>DNA

<213>Diabrotica?virgifera

<400>40

<210>41

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>41

<210>42

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>42

<210>43

<211>569

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>43

<210>44

<211>440

<212>DNA

<213>Diabrotica?virgifera

<400>44

<210>45

<211>46

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>45

<210>46

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>46

<210>47

<211>1113

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>47

<210>48

<211>425

<212>DNA

<213>Diabrotica?virgifera

<400>48

<210>49

<211>42

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>49

<210>50

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>50

<210>51

<211>47

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>51

<210>52

<211>95

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>52

<210>53

<211>427

<212>DNA

<213>Diabrotica?virgifera

<400>53

<210>54

<211>43

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>54

<210>55

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>55

<210>56

<211>318

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>56

<210>57

<211>431

<212>DNA

<213>Diabrotica?virgifera

<400>57

<210>58

<211>47

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>58

<210>59

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>59

<210>60

<211>328

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>60

<210>61

<211>483

<212>DNA

<213>Diabrotica?virgifera

<400>61

<210>62

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>62

<210>63

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>63

<210>64

<211>503

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>64

<210>65

<211>407

<212>DNA

<213>Diabrotica?virgifera

<400>65

<210>66

<211>42

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>66

<210>67

<211>40

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>67

<210>68

<211>345

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>68

<210>69

<211>456

<212>DNA

<213>Diabrotica?virgifera

<400>69

<210>70

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>70

<210>71

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>71

<210>72

<211>472

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>72

<210>73

<211>503

<212>DNA

<213>Diabrotica?virgifera

<400>73

<210>74

<211>42

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>74

<210>75

<211>47

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>75

<210>76

<211>417

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>76

<210>77

<211>927

<212>DNA

<213>Diabrotica?virgifera

<400>77

<210>78

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>78

<210>79

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>79

<210>80

<211>912

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>80

<210>81

<211>342

<212>DNA

<213>Diabrotica?virgifera

<400>81

<210>82

<211>42

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>82

<210>83

<211>42

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>83

<210>84

<211>344

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>84

<210>85

<211>674

<212>DNA

<213>Diabrotica?virgifera

<400>85

<210>86

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>86

<210>87

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>87

<210>88

<211>538

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>88

<210>89

<211>551

<212>DNA

<213>Diabrotica?virgifera

<400>89

<210>90

<211>40

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>90

<210>91

<211>47

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>91

<210>92

<211>407

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>92

<210>93

<211>401

<212>DNA

<213>Diabrotica?virgifera

<220>

<221>misc_feature

<222>(369)..(369)

＜223〉n is a, c, g, or t

<400>93

<210>94

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>94

<210>95

<211>46

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>95

<210>96

<211>348

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>96

<210>97

<211>1168

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>97

<210>98

<211>2131

<212>DNA

<213>Diabrotica?virgifera

<400>98

<210>99

<211>1720

<212>DNA

<213>Diabrotica?virgifera

<400>99

<210>100

<211>1175

<212>DNA

<213>Diabrotica?virgifera

<400>100

<210>101

<211>1176

<212>DNA

<213>Diabrotica?virgifera

<400>101

<210>102

<211>2410

<212>DNA

<213>Diabrotica?virgifera

<400>102

<210>103

<211>1575

<212>DNA

<213>Diabrotica?virgifera

<400>103

<210>104

<211>1870

<212>DNA

<213>Diabrotica?virgifera

<400>104

<210>105

<211>24

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>105

<210>106

<211>24

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>106

<210>107

<211>23

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>107

<210>108

<211>23

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>108

<210>109

<211>20

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>109

<210>110

<211>20

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>109

<210>111

<211>21

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>111

<210>112

<211>21

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>112

<210>113

<211>19

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>113

<210>114

<211>19

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>114

<210>115

<211>20

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>115

<210>116

<211>20

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>116

<210>117

<211>21

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>117

<210>118

<211>21

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>118

<210>119

<211>20

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>119

<210>120

<211>19

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>120

<210>121

<211>43

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>121

<210>122

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>122

<210>123

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>123

<210>124

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>124

<210>125

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>125

<210>126

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>126

<210>127

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>127

<210>128

<211>40

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>128

<210>129

<211>40

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>129

<210>130

<211>41

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>130

<210>131

<211>40

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>131

<210>132

<211>40

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>132

<210>133

<211>40

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>133

<210>134

<211>39

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>134

<210>135

<211>36

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>135

<210>136

<211>56

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>136

<210>137

<211>53

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>137

<210>138

<211>26

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>138

<210>139

<211>25

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>139

<210>140

<211>53

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>140

<210>141

<211>608

<212>DNA

<213>Diabrotica?virgifera

<400>141

<210>142

<211>533

<212>DNA

<213>Diabrotica?virgifera

<400>142

<210>143

<211>1114

<212>DNA

<213>Diabrotica?virgifera

<400>143

<210>144

<211>1125

<212>DNA

<213>Leptinotarsa?decemlineata

<400>144

<210>145

<211>1125

<212>DNA

<213>Spodoptera?frugiperda

<400>145

<210>146

<211>1126

<212>DNA

<213>Agrotis?ipsilon

<400>146

<210>147

<211>1126

<212>DNA

<213>Helicoverpa?zea

<400>147

<210>148

<211>1126

<212>DNA

<213>Ostrinia?nubilalis

<400>148

<210>149

<211>1125

<212>DNA

<213>Anthonomus?grandis

<400>149

<210>150

<211>1125

<212>DNA

<213>Tribolium?castaneum

<400>150

<210>151

<211>2860

<212>DNA

<213>Manduca?sexta

<400>151

<210>152

<211>3097

<212>DNA

<213>Aedes?aegypti

<400>152

<210>153

<211>2533

<212>DNA

<213>Drosophila?melanogaster

<400>153

<210>154

<211>603

<212>DNA

<213>Bombyx?mori

<400>154

<210>155

<211>612

<212>DNA

<213>Drosophila?melanogaster

<400>155

<210>156

<211>567

<212>DNA

<213>Anopheles?gambiae

<400>156

<210>157

<211>652

<212>DNA

<213>Diabrotica?virgifera

<400>157

<210>158

<211>402

<212>DNA

<213>Anthonomus?grandis

<400>158

<210>159

<211>403

<212>DNA

<213>Tribolium?castaneum

<400>159

<210>160

<211>23

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>160

<210>161

<211>24

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>161

<210>162

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>162

<210>163

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>163

<210>164

<211>45

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>164

<210>165

<211>44

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>165

<210>166

<211>22

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<400>166

<210>167

<211>26

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<220>

<221>misc_feature

<222>(23)..(23)

＜223〉n is a, c, g, or t

<400>167

<210>168

<211>25

<212>DNA

＜213〉artificial sequence

<220>

＜223〉synthetic

<220>

<221>misc_feature

<222>(6)..(6)

＜223〉n is a, c, g, or t

<400>168

<210>169

<211>2713

<212>DNA

<213>Diabrotica?virgifera

<400>169

<210>170

<211>1363

<212>DNA

<213>Diabrotica?virgifera

<400>170

<210>171

<211>1215

<212>DNA

<213>Diabrotica?virgifera

<400>171

<210>172

<211>3363

<212>DNA

<213>Diabrotica?virgifera

<400>172

<210>173

<211>843

<212>DNA

<213>Diabrotica?virgifera

<400>173

<210>174

<211>704

<212>DNA

<213>Diabrotica?virgifera

<400>174

Claims (18)

1. be used to reduce or eliminate the transgenic event that piles up of plant pest invasion and attack, comprise and suppress in the target pest dsRNA of important function of gene very and show bioactive insecticide at described target pest.

2. the transgenic event that piles up of claim 1, wherein said incident is the plant that is selected from by the following group that constitutes: alfalfa, dill (aneth), apple, apricot, artichoke, rocket salad, asparagus, avocado, banana, barley, beans, beet (beet), blackberry, blueberry, blueberry, cabbage, brussels sprouts, cabbage, leaf mustard, muskmelon, carrot, cassava, cauliflower, celery, cherry, coriander, oranges and tangerines, the little oranges and tangerines of Ke Laimenshi, coffee, corn, cotton, cucumber, pesudotsuga taxifolia, eggplant, hare's-lettuce, wide leaf lettuce, eucalyptus, fennel, fig, cucurbit, grape, shaddock, Hami melon, yam bean, Chinese grooseberry, lettuce, leek, lemon, bitter orange, torch pine, mango, melon, mushroom, nut, oat, okra, onion, tangerine, decorate and use plant, pawpaw, parsley, pea, peach, peanut, pears, pepper, persimmon, pine tree, pineapple, plantain, Lee, pomegranate, white poplar, potato, pumpkin (pumpkin), Wen Bai, pine, witloof, radish, raspberry, paddy rice, naked barley, Chinese sorghum, the south pine, soybean, spinach, pumpkin (squash), strawberry, beet (sugarbeet), sugarcane, sunflower, Ipomoea batatas, storax, mandarin orange, tea, tobacco, tomato, turf, vining plant, watermelon, wheat, Chinese yam and Xiao Hu's melon plant.

3. the transgenic event that piles up of claim 1, wherein said very important function of gene is the target gene of coded protein, the function of its prediction is selected from the group that is made of following function: muscle forms, the formation of juvenile hormone, the regulation and control of juvenile hormone, ion regulation and control and transhipment, synthesizing of digestibility enzyme, the maintenance of cell membrane gesture, amino acid bio is synthetic, amino acid degradation, sperm form, pheromones synthetic, the pheromones sensing, the formation of feeler, wing forms, the formation of ovum is grown and differentiation in the formation of leg, the larva maturation, the formation of digestibility enzyme, hemolymph synthetic, the maintenance of hemolymph, neurotransmission, cell division, energy metabolism is breathed and apoptosis.

4. the transgenic event that piles up of claim, wherein said insecticide is the reagent that is selected from by the following group that constitutes: potato tubers storage protein patatin, Bacillusthuringiensis insecticidal protein, Xenorhabdus insecticidal protein, Photorhabdus insecticidal protein, Bacillus laterosporous insecticidal protein and Bacillussphearicus insecticidal protein.

5. the transgenic event that piles up of claim 4, wherein said Bacillusthuringiensis insecticidal protein is selected from the group that is made of following: Cry1, Cry3, TIC851, CryET70, Cry22, double base insecticidal protein CryET33 and CryET34, double base insecticidal protein CryET80 and CryET76, double base insecticidal protein TIC100 and TIC101 and double base insecticidal protein PS149B1.

6. the transgenic event that piles up of claim 1, wherein said target pest is the agriculture pest that is selected from by the following group that constitutes: insect, mite, fungi, yeast, mould, bacterium, nematode, weeds and parasite and saprophyte.

7. the transgenic event that piles up of claim 6, wherein said agriculture pest is selected from the group that is made of following: insect pest and nematode pest.

8. the transgenic event that piles up of claim 6, wherein said agriculture pest is the insect pest that is selected from by the following group that constitutes: Lepidoptera pest, coleoptera pest, Semiptera pest and diptera pest.

9. the transgenic event that piles up of claim 8, wherein said coleoptera pest is selected from by Diabrotica species, Colorado potato bug (CPB, Leptinotarsadecemlineata) and the group that constitutes of red flour beetle (RFB, Tribolium castaneum); Described Lepidoptera pest is selected from by European corn borer (ECB, Ostrinianubilalis), black cutworm (BCW, Agrotis ipsilon), Heliothis zea (CEW, Helicoverpa zea), autumn armyworm (FAW, Spodoptera frugiperda), the group of boll weevil (BWV, Anthonomus grandis), silkworm (Bombyx mori) and Manduca sexta formation; Described Semiptera pest is a lygus bug.

10. the transgenic event that piles up of claim 9, wherein said Diabrotica species is selected from the group that is made of Diabrotica virgifera, Diabrotica barberi and Diabroticaundecimpunctata.

11. the transgenic event that piles up of claim 1, wherein said incident is provided in the meals of described target pest with the pest amount of suppression, and suppresses the described pest described meals of taking food.

12. the transgenic event that piles up of claim 11, wherein said meals are selected from by the root of plant cell, various plants cell, plant tissue, plant, plant seed and the group that plant constituted of coming from the plant seed growth, wherein, described meals comprise the described dsRNA and the described insecticide of pest amount of suppression.

13. the transgenic event that piles up of claim 2, pest invasion and attack wherein said minimizing or that eliminate have improved the output of the crop that is produced by described incident.

14. by the crop of the field of the transgenic event that piles up that comprises claim 2 results, wherein said crop comprises described dsRNA and described insecticide.

15. by the seed that the transgenic event that piles up of claim 13 is produced, wherein said seed comprises the gene of the described dsRNA of coding of detectable amount.

16. by the agricultural product or the agricultural product goods of the crop production of claim 14, wherein said agricultural product or agricultural product goods comprise the gene of the described dsRNA of coding of detectable amount.

17. the transgenic event that piles up of claim 2, wherein said dsRNA in the cell of described plant and described insecticide comprise seed treatment.

18. the transgenic event that piles up of claim 17, the cell of wherein said plant comprise described dsRNA and described insecticide.