CN100510074C - Promotor induced by resistance inducer acquired by paddy system - Google Patents

Abstract

A promoter fragment for separating and utilizing nucleic acid is prepared from the gene in response with the induction of PBZ and relative compound in paddy rice. Said nucleic acid sequence of the target gene is combined with said promoter to obtain a recombinant DNA, which is used to transform plant for obtaining transgenic plant.

Description

A kind ofly be subjected to paddy rice systemic acquired resistance inductor inductive promotor and application thereof

Technical field

The invention belongs to molecular biology of plants and gene engineering technology field.Be specifically related to a kind of be subjected to paddy rice systemic acquired resistance inductor inductive promotor and application thereof.This promotor derives from the paddy rice the regional sequence of the upstream non-transcribed of allyl isothiazole (PBZ, Probenazole, 3-allyloxy-2-phenylpropyl alcohol isothiazole-1,1-dioxide) and related activity product evoked response gene thereof.This promoter fragment can be by means of near the expression of gene inductor PBZ initial sum driving downstream in unifacial leaf and dicotyledons.Make up recombinant expression vector with this promoter fragment and transform plant, can obtain novel transgenic plant.In these novel transgenic plant, PBZ and related activity product (BIT) thereof can optionally be induced the expression and the regulation and control of target gene.

Background technology

In more than ten years, people have obtained up to a hundred the functional genes that significant application value is arranged in crop genetic improvement in the past.Along with the progress of functional genome research, people also can clone the functional gene that is widely used and is worth in bulk.These multifarious genetic resourceses will be used to improve on a large scale crop and other important plant; cause the demand growing so that satisfy the population growth to grain; alleviate the immense pressure of environmental improvement and protection, and provide abundant daily necessities and high-quality living environment for the town dweller.These multifarious functional gene resources need could play a role under the regulation and control of dissimilar promotors rightly.

In general, promotor is the section of DNA that is positioned at the gene coding region upstream, comprises transcription initiation region.Promoter region comprises the element of multiple regulate gene expression simultaneously, as approximately being positioned at the TATA box of transcription initiation site upstream 30 bp (30) position, and the CAAT box that is positioned at 75 bp positions, upstream.Also comprise the controlling element that to respond to other extraneous factors in the plant promoter,, and then genes involved carried out expression regulation such as environmental factors such as light, chemical substance, nutritional condition, heat, anoxic, heavy metals.Other dna sequence dna in the promotor is relevant with the tissue specificity of the sequential of growth or genetic expression.Also there is enhancer sequence in the eucaryon system, near expression of gene level can improving greatly; These reinforcing effects position residing with it and direction are had little or nothing to do with.

In recent years, plant gene engineering technology is aspect the genetic improvement of crop varieties, particularly in disease-resistant worm characteristic and antiweed characteristic, and obtained achievement and the progress that attracts people's attention on the cereal kernel quality-improving, and also more and more demonstrated its huge application potential in many others, as structure of plant bioreactor etc.Yet, when obtaining these breakthroughs, caused also that about ecological safety and the food-safety problem of transgenic plant the public more and more pays close attention to, argues even protests.Except irrational and non-science factor, also there are its intrinsic limitation really in existing selected gene and objective function expression of gene system in the middle of this.Under the state of nature, the intragentic expression of organism all is subjected to strict regulation and control.Regulatory factor may be that developmental process is relevant, and the sequencing that shows as gene is expressed, and comprises spatial and temporal expression; May be the environmental factor inductive also, the emergency that shows as gene be expressed.Yet at present used promotor mostly is composing type in the plant genetic engineering, and the promotor of these composing types orders about the selected marker and the objective function gene continues to efficiently express, for the safety issue of transgenic technology and transgenic plant has been buried hidden danger.In fact, the selected marker only need express when the screening transformant; Objective function gene in disease-resistant worm, antiweed and the bio-reactor also just needs to express in the specific stage of growing, in the time of many even only be of short duration expression.For plant, the invalid continuous expression of foreign gene is not only the unnecessary consumption of matter and energy, but also disturbs the normal physiological activity of vegetable cell, the yield and quality of influence results organ, even also can cause consequence such as proterties forfeiture.Take and find at Bt (Bacillus thuringiensis) toxic protein transgenic cotton recently, the toxicity in vivo protein gene is expressed for a long time, easily cause bollworm that toxic protein is produced resistance (Mcaughey et al., Nature biotechnol.16:144-146.1998).Also there is similar problem with plant as bio-reactor.For ecotope, the foreign gene of continuous expression may shift between nearly edge species by pollen or other approach, cause having the part selected gene of potential hazard or the proterties of functional gene and control thereof to be escaped, and then whole food chain and species diversity are caused the consequence that is difficult to expect.

In order to overcome constitutive promoter these shortcomings in plant genetic engineering, people have considered to develop inducible promoter, tissue specificity/etap specificity promoter.Inducible promoter is applied to plant genetic engineering many outstanding advantages, is mainly reflected in: 1, objective function gene abduction delivering as required; 2, the expression of gene level can be adjusted by the intensity of regulating inductor/factor; 3, by using different inductor/combinations of factors can regulate the coordinate expression of correlation function gene.

On plant, the wound-induced expression system be early be studied, attempt to be used for the engineered a kind of inducible expression system of disease-resistant worm (Lorberth et al., PlantJ.2:477-86.1992).But because this class promotor is to induce objective function genetic expression by means of the wound that the infringement of sick worm causes, the speed of the disease-resistant worm genetic expression of institute's inductive and undercapacity to be producing resistance timely and effectively, thereby can not produce ideal resistance effect.In addition, other physical abuse as Storms etc., also can cause the unnecessary expression of disease-resistant worm gene.

Secondly, the promotor of the maize alcohol dehydrogenase Adh I gene of hypoxia inducible may be one of inducible promoter of studying the most detailedly.

By the method for electroporation, the maize alcohol dehydrogenase Adh I gene transformation of hypoxia inducible is come from the corn protoplastis of suspension culture.Protoplastis after the conversion places the low oxygen content place, and in the expression of 20 hours post analysis Adh I.Express for ease of the Adh I that measures hypoxia inducible, natural A dh I gene 5 ' regulation and control fragment (1096 bp) is linked to each other with CAT.Their result shows that in the protoplastis that comes from the homologous culturing cell, the anoxia condition of standard can be regulated and control the Adh I promotor/CAT gene of monocotyledons corn.Simultaneously, they find again, in the corn protoplastis, the promoter fragment of Adh I itself just is enough to respond inducing of anoxia condition, and then the regulation and control expression of exogenous gene, need not (the Howard that exists in coding region and 3 ' district, et al., Planta, 170:535-450.1987).

Other investigators have further determined the corn Adh I gene dna fragmentation relevant with hypoxia inducible.These investigators change the recombination that comprises CAT encoding sequence and Adh I promotor in the corn protoplastis, detect the CAT activity after 24 hours.By changing the length of promoter fragment, people such as Lee determine to be enough to from the initiator sequence of transcription initiation site upstream 146 bp the expression of startup CAT under anoxic condition.Yet promoter sequence after 5 ' end continues to extend to 266 or 955 bp, CAT expression amount risen 5 or 8 times (Lee et al., Plant Physiology 85:327-330,1987).

People such as Walker continue to be subjected to moment expression method research corn Adh I upstream region of gene the sequence of hypoxia inducible promotor gene expression.They have determined 2 sections relevant with the genetic expression of hypoxia inducible in promotor sequences :-133--124 and-113--99 (transcription initiation site upstreams).These 2 sections sequences are necessary for inducing.Before the viral promotors of affinity-less relation, can obtain hypoxia inducible performance (Walker et al., proc.Natl.Acad.Sci.USA 84:6624-6628,1987) behind the element of this section of interpolation 40bp.

The someone finds in the tobacco cell of stable conversion in addition, if with corn Adh I gene-1 094-+106 these section regulation and control CAT gene, under suitable anoxia condition, low-down CAT genetic expression is arranged.In fact, only detect the mRNA of CAT.Yet, the promoter element of octopine synthase gene or cauliflower mosaic virus (CaMV) is connected on 5 ' end of Adh I promotor, the expression that can stimulate CAT, and behind hypoxia inducible, detect CAT.Comprise the fragment with Adh I genetic transcription initiation site 5 ' flanking sequence 247bp, be enough to the CAT expression of gene is placed under the hypoxia regulatory.Therefore, even under the condition of octopine synthetic enzyme that composing type is arranged or the existence of CaMV 35S promoter fragment, the existence of the order of this section 247bp still makes expression of gene be subjected to hypoxia regulatory (Ellis et al., EMBO Journal 6:11-16,1987).People such as Howard, Lee and Walker by moment the Adh I promoter region that is subjected to the hypoxia inducible regulation and control that obtains of expression analysis with people such as Ellis by the stable conversion plant obtained consistent or similar.

Because the promotor evoked response factor of Adh I gene is an anoxic condition, thereby the application on genetically modified crops does not have the operability of reality.

In numerous inducible promoters, chemical inducible promoter has many outstanding advantages on the regulation and control expression of exogenous gene, and wherein topmost advantage is that controllability is strong.Efficiently, single-minded chemically inducible promoter can be used for the safely expressed of all kinds functional gene in theory, optimal may be to be used for plant genetic engineering of disease-resistant worm and the structure of bio-reactor plant.

The inductor of existing much energy regulating expression of foreign genes/promotor combination in bacterium and animal system.The system of inducing in many bacteriums is based on the promotor that can respond metabolite or its analogue.After comprising promoter related target gene transform bacteria, in its substratum, add suitable inductor, just can cause the expression of target product.Sophisticated inductor/promotor combination comprises 3-β-indolylacetic acid/trp promoter, the IPTG/lac promotor, and the hungry evoked promoter of phosphate/phosphate, and L-arabinose/ara B promotor etc.Similarly, heavy metal/metallothionine promotor, oneself is applied to promotors such as heat/heat-shocked in the culture systems of zooblast, the regulation and control expression of exogenous gene.

On plant, the herbicide-safener evoked promoter is the practical chemically inducible promoter that a class is studied more deeply, but because aspects such as its inducing specific remain in some problems, (Hershey et al. at present as yet is not widely used, Plant Mol Biol.17:679-690,1991).The U.S. once ratified the patent of a herbicide-safener inductive promotor, and (U.S. Patent number: 5364780), the investigator has obtained patent (1991 years) with first " be applicable to chemical substance that the land for growing field crops produces is induced and in transgenic plant the promotor of goal of regulation and control genetic expression ".In further using, they link to each other the In2-2 promotor with reporter gene GUS, the arabidopsis thaliana transformation plant, find by histochemical methods analyst, for dissimilar herbicide-safeners, GUS is expressed in (De Veylder L et al., Plant CellPhysiology in the different tissues such as root, seedling respectively, 38 (5): 568-577,1997).

Chemical inducible promoter of other report has Whitfield's ointment, dextran acceptor, Cu2+, alcohols, tsiklomitsin, female hormone, growth hormone, cytokinin, gibberic acid, evoked promoter such as ethene and dormin (Davies, P. (Ed.) PlantHormones and Their roles in Plant Growth and Development, Martinus Nijhoff Publ.1987; Ebel et al., 1984).These promotors are mainly used in theoretical investigation, do not possess actual application value.

Chemical induction material used in the present invention---PBZ is to produce to go up the inductor that uses botanical system acquired resistance for many years, has many superiority.At first, this medicament is grown no significant adverse influence to the normal growth of plant, pathogenic bacteria there is not direct toxicity yet, be difficult for causing resistance, its inducing anti-disease mechanism mainly realizes (Sakamoto et al. by a series of Expression of Related Genes in the regulation and control body on transcriptional level, Plant Mol Biol.40:847-855,1999; Yoshioka et al., Plant is (2) J.25: 149-157,2001; Ding Derong, the post-doctor of Fudan University report of setting off, 2001).Secondly, it is a kind of efficient disease-resistance inductor of preventing and treating rice blast, can alleviate the 80-90% that causes production loss by rice blast, and effect stability, become the disease-resistant inductor (Zeigler of South East Asia Dao Qu control rice blast usable floor area maximum, Leogler and Teng (Ed.) Strategies for the discovery of rice blast fungicides.in:Rice Blast Disease, CAB International Press.1994).At last, inhale transporting in allyl isothiazole has in plant materials, having overcome inductors such as Whitfield's ointment can not transporting in plant materials, easily cause the shortcoming (Kessmann, et al., Annu Rev Phytopathol.32:439-459,1994) of plant poisoning.

In sum, the application of allyl isothiazole in agriculture production has very big operability, thereby most possibly is applied to the expression of goal gene in the transgenic plant of land for growing field crops.It is reported, allyl isothiazole can inducing paddy rice in the enhancing of some disease-resistant related genes express, as the RPRl gene.The coded product of this gene contains leucine enrichment iteron (LRR) and nucleic acid binding site (NBS), and these are the common features of many known disease-resistant genes.The RPR1 expression of gene can also be by the commonly used acquired disease resistance of botanical system (SAR) inductor BTH and SA, and the inducing of pathogenic bacteria (Sakamoto et al., Plant Mol Biol.40:847-855,1999).Discovering on Arabidopis thaliana, PBZ or its active metabolite BIT also can inducible system acquired resistances (SAR).Different with common chemical inductor BTH and INA, PBZ is by activating the defence signal pathway that the SA upstream becomes to assign to activate the SA/NPRl mediation, and then induce SAR, and the former is seemingly as the analogue of SA (the Yoshioka et al. that plays a role, Plant is (2) J.25: 149-157,2001).

Yet up to now, induce the research that strengthens the promotor of expressing genes involved not appear in the newspapers as yet, also do not have the report of in the transgenic plant body, regulating and control the induced system of corresponding promotor and structure gene combination by PBZ to PBZ.

The present invention uses difference to subtract the inhibition hybridization technique, and by means of the approach of information biology, separates being subjected to PBZ to induce the promotor of the gene of rise from paddy rice, identifies that they are to PBZ evoked response level.These promoter fragments can be used to set up the gene induced expression system of a cover, regulate and control expression of exogenous gene in transgenic plant.

Summary of the invention

The object of the present invention is to provide a kind ofly to be subjected to botanical system acquired resistance inductor inductive promotor and application thereof, so that the selective expression of gene in applied chemistry material control transgenic plant and the plant tissue.

The botanical system acquired resistance inductor inductive promotor that is subjected to provided by the invention is to come from the nucleic acid promoter fragment of paddy rice to the PBZ evoked response.Oneself is building up to these nucleic acid promoter fragments in the recombinant vectors that contains non-plant source gene, and the expression level of discovery structure gene is subjected to the induction regulating controlling of PBZ behind the conversion plant.Therefore after inducing with PBZ, the expression level of the target gene that is connected with this promoter fragment in the transgenic plant will rise.

Above-mentioned said nucleic acid promoter can obtain from most crops, monocotyledons such as paddy rice, corn, oat, wheat, grass, barley, Chinese sorghum, onion and sugarcane; Dicotyledons such as Arabidopis thaliana, clover, soybean, petunia, cotton, beet, cucumber, tomato, tobacco, pea etc.Most importantly the nucleic acid promoter that from paddy rice, obtains.

The above-mentioned said one group of nucleic acid promoter fragment that comprises is the nucleotide sequence in rice Os PIG-1 (Oryza sativa Probenazoleinducible gene-1) gene (SEQ ID No.1) 5 ' upstream promoter zone.The transgenic plant that have described promoter fragment can cause that after handling with PBZ the expression of the target gene that is connected described promotor 3 ' end raises.In paddy rice, the regulatory nucleotide sequence in this gene 5 ' upstream promoter zone can be SEQ ID No.3 or SEQ ID No.4 etc.These sequences comprise and are subjected to PBZ inductive element and different tissue specific expression element etc.Described nucleotide sequence can hybridized with the Nucleotide that is fixed on the SEQ ID No.2 on the solid support film under the moderate stringent condition, through 0.1 X SSC, 0.1% SDS is behind 50 ℃～65 ℃ wash-outs, and exposure can obtain the radioautograph signal after 24 hours to the X-mating plate at-80 ℃.

Another aspect of the present invention is relevant with a recombinant DNA carrier.This carrier contains above-mentioned nucleotide sequence as promotor.This carrier can transform plant, the dna sequence dna of the coding specific objective gene that comprise a nucleic acid promoter fragment among the present invention, links to each other and 3 ' suitable downstream sequence with this promotor, make the plant that transforms behind this recombinant vectors under the effect that Compound P BZ is arranged, specific objective gene transcription product level rises.Target gene has the coding gus gene among the present invention, resistant genes such as coding resisting bacterial leaf-blight, rice blast, the encode gene of anti-insect, the proteins encoded enzyme inhibitor gene, the endotoxic gene of coding Bacillusthuringenesis insect, the gene of coded plant ethene biosynthetic enzyme, the gene of coded plant hormone biosynthetic enzyme, the gene of coding male sterile/fertility phenotype, the gene of coding calmodulin, the gene of various vaccines of encoding, and the gene of various medicinal or edible compositions etc. of encoding.

Another aspect of the present invention is to comprise with recombinant DNA sequence plant transformed of the present invention, and this transgenic plant are handled with Compound P BZ and induce the target gene expression amount to increase, and this gene order is through being operatively connected 3 ' end at described promoter fragment.The seed of such transgenic plant is regarded as the embodiment of this invention equally.

Last aspect of the present invention is included in the method that causes in the plant that destination gene expression increases, and it is made up of several steps: a) with above-mentioned recombinant DNA thaumatropy plant; B) handle transgenic plant with Compound P BZ; C) the render transgenic plant increases the content of target gene product at the developmental stage of expectation.

Embodiment

1, paddy rice is cultivated, PBZ handles, material is collected and disease resistance is identified

Get an amount of seed rice, soak a moment, remove shrivelled kernel with tap water.With 3% superoxol sterilization 30min, discard hydrogen peroxide afterwards again, soaked seed 3 days with aseptic tap water down for several times and at 30 ℃ with aseptic tap water washing.After treating that seed shows money or valuables one carries unintentionally, be layered on equably on the enamel tray that is lined with 4 layers of sterile gauze, under 27 ℃, the dark 8h cycle of illumination 16h/ cultivated 7 days down.Use the 100ppm allyl isothiazole to handle paddy rice at the 1-9 day respectively afterwards, processing mode is the root solution soaking.All inoculate rice blast fungus after the processing, inoculation method is: put in the inoculation tank, under 26 ℃, relative humidity is to carry out spray inoculation under the condition more than 85%, inoculation liquid concentration is 1 x 10 ⁵Spore/milliliter, the 24hr that preserves moisture after the inoculation takes out and puts spraying and moisturizing in the cool canopy, the 7d " Invest, Then Investigate " state of an illness.

Handle back the 1st, 2,3,4,5,6,7,8 by inoculation, 9,10,12 days time gradient is collected root, the leaf texture of paddy rice, and liquid nitrogen flash freezer places-70 ℃ of preservations.

2, the extracting of the total RNA of paddy rice

Take out all used vessel of RNA and all use DEPC water treatment or 200 ℃ of bakings of 0.1%, to remove the RNA enzyme.

(1) the total RNA of hot phenol method extracting paddy rice

Water intaking rice material 2g places mortar, adds liquid nitrogen and fully is ground to finely powdered, transfer to immediately in the 10ml centrifuge tube, add the extraction buffer 4ml that is preheated to 90 ℃, the thermal agitation mixing, add the 2ml chloroform behind the 3min, shake mixing 15-20min, 12, the centrifugal 15min of 000g sucts clearly, adds the 8M LiCl of 1/3V, mixing is placed 16hr, centrifugal collecting precipitation down for 4 ℃, use 2M LiCl and 80% washing with alcohol 2 times respectively, room temperature is dried, and precipitation is dissolved in the 100ulDEPC water.

(2) the total RNA of Trizol method extracting paddy rice

Packing 1ml trizol reagent is marked.An amount of rice tissue is taken out from refrigerator, in liquid nitrogen, grind to form fine powder rapidly.Powder is put into the 1.5ml centrifuge tube that is added with 1ml TRIzol reagent, firmly shake up the back room temperature and leave standstill 5min (can put temporarily under 4 ℃ then); Add the 0.2ml chloroform and shake up, room temperature is placed 3min, and 4 ℃ down 13, the centrifugal 15min of 000g gets upper water phase transition to a new centrifuge tube.Aqueous phase adds the 0.5ml Virahol, precipitation at room temperature 10min, and 4 ℃ are descended 13, and the centrifugal 15min of 000g removes supernatant.The washing with alcohol precipitation that adds 1ml 75%, 13, the centrifugal 5min of 000g removes most supernatant.Be deposited in drying at room temperature 5min with thorough removal ethanol.Add the aseptic DEPC water dissolution of 20 μ l RNA, get 1 μ l and dilute, measure O.D. with 1:1000 ₂₆₀With O.D. ₂₈₀Ultraviolet absorption value, other gets 1 μ l RNA and carries out electrophoresis, determines concentration and the purity of RNA.

3, mRNA separation and purification

The mRNA separation and purification is undertaken by mRNA Purification Kit explanation.

4, suppress subtractive hybridization (SSH)

Concrete operations are undertaken by Clontech test kit specification sheets.

5, difference subtracts the structure (T/A cloning) in cDNA library

Forward behind pcr amplification and oppositely poor subtracting the cDNA colony (25ul altogether) are taken out 3ul, 1 μ l pGEM-TEasy Vector (50 ng), 1U T4 dna ligase joins mixing in 1 * T4 ligase enzyme damping fluid, 4 ℃ down connection spend the night.After ligation is finished, reaction solution is joined in the 100 μ l escherichia coli jm109 competent cells ice bath 30min, 42 ℃ of following heat shock 90s are transferred to rapidly and place 3-5min on ice, add the liquid LB substratum 300 μ l of 37 ℃ of preheatings, place 37 ℃ of shaking tables again, 150rpm cultivates 60min.With cultured bacterium liquid 200 μ l with coat on the LB flat board that contains 100 μ g/ml penbritins after 40 μ l X-gal solution (10mg/ml), 4 μ l IPTG solution (10mg/ml) mix.Be inverted down for 37 ℃ and cultivate 15h.Picking white clone on the X-gal/lPTG agar plate, dibbling is in 96 orifice plates that fill liquid LB, and overnight incubation adds 15% glycerine, liquid nitrogen flash freezer ,-80 ℃ of guarantors plant standby.

Be inoculated in respectively and be equipped with in the test tube of liquid LB that 2ml contains 100 μ g/ml penbritins protecting kind of plasmid, place in the shaking table under 37 ℃ the 240rpm overnight incubation.Alkaline process extracting next day plasmid.At first bacterium liquid is transferred in the 1.5ml centrifuge tube, 13, the centrifugal 1min of 000g removes supernatant, adds the solution I of 100 μ l ice precooling, and vibration is beaten somatic cells even; The solution II that adds the new configuration of 200 μ l again, room temperature is placed 3min; Add the solution III of 150 μ l ice precooling, place 5min on ice; Then 13, the centrifugal 10min of 000g collects supernatant, adds 2 times of volume ethanol, precipitation at room temperature 2min; 13, the centrifugal 10min of 000g removes supernatant and adds 70% washing with alcohol once, and again with 13, the centrifugal 2min of 000g removes most supernatant and uncaps under room temperature and dry 5min.Add 40 μ l sterilized waters dissolving plasmid at last.

6, differential screening difference subtracts the cDNA library

First round differential screening

(1) plasmid sample spot film

200 recon numberings of picking, the extracting plasmid adds 1ul plasmid (200ng)/9ulH in each aperture respectively ₂O/10ul0.6NNaOH, mixing.(two covers in preparation cDNA library repeat to copy film) carries out record.Room temperature is dried 30min, and nylon membrane contains one of DNA and faces up, floating 0.5M Tris-HCl (pH7.5) the neutralizer 2-4min that places, and rinsing in sterilized water is dried, and uv irradiating is fixed.

(2) differential probe preparation

Getting the forward difference respectively subtracts hybridization cDNA and (handles with PBZ and to make Tester, Driver is made in non-processing) and the oppositely poor hybridization cDNA that subtracts (with the non-Tester of being treated to, be treated to Driver with PBZ) pcr amplification product 40ul (～400-1600ng), PCR product purification test kit reclaims the PCR product.Successively (15units, 37 ℃, 1hr), (1hr), (10units, 37 ℃, 1hr) enzyme is cut the joint of digestion with abundant removal cDNA molecule two ends to EaeI to SmaI for 10units, R.T with RsaI.Enzyme is cut product and is reclaimed with PCR product purification test kit equally, is the differential screening probe.Probe mark adopts random primed DNA labeling system.

(3) dot blot

Get about 200ng forward difference respectively and subtract cDNA and the oppositely poor cDNA of subtracting colony label probe, two covers that two kinds of probes are used for hybridizing same cDNA library respectively repeat to copy film.68 ℃ of conditions of dot blot employing (6xSSC/5xDenhardt ' the s/0.1%SDS/100ug/ml salmon sperm DNA).Wash the film condition and be (2xSSC/0.5%SDS, 68 ℃, 4x20min; 0.2xSSC/0.5%SDS, 68 ℃, 4 x 20min).

Second takes turns the differential screening

Get the cDNA recon plasmid of primary dcreening operation, insert segment with a pair of universal primer T7/SP6 amplification external source of pGEM-T.The PCR system is: 20ng plasmid template/0.5uM SP6/1 unit Tag/200uM dNTPs/2ul 10xPCR reaction buffer.The PCR response procedures is: 94 ℃ of 5min, 60 ℃ of 2min, 72 ℃, 2min, 1 circulation; 95 ℃ of 30s, 60 ℃ of 100s, 72 ℃ of 2min, 30 circulations; 72 ℃ prolong 7min.Get the 3ulPCR product, point sample is in 2%Agarose/EB/1xTAE, and the 5V/cm electrophoresis changes film (annotate: preparation two covers repeat to copy film).

Getting about 100ng forwards/reverse difference respectively subtracts cDNA colony and prepares radioactive probe.Two covers that two kinds of probes are used for hybridizing the PCR product respectively repeat to copy film, hybridization, and it is the same to wash the film condition.

7, Northern hybridization analysis

(1) preparation Northern Hybond membrane

Take by weighing a certain amount of agarose (final concentration in glue is 1%), add suitable quantity of water, heating makes the agarose dissolving, does the cooling back slightly and adds formaldehyde (final concentration 2.2mol/L) and MOPS damping fluid (final concentration be 1 *).During gelling is solid, handle RNA.Every kind of RNA sample is got 40 μ g, adds formaldehyde (final concentration 2.2mol/L), methane amide (final concentration is 50%), MOPS electrophoretic buffer (final concentration 0.5 *), and mixing places 65 ℃ of water-bath 15min, is placed on rapidly after the taking-up and leaves standstill 3min on ice.Sample is splined on denaturing formaldehyde glue after adding sample-loading buffer, walk electrophoresis by the voltage of 3-4V/em in 1 * MOPS damping fluid down at 4 ℃.Electrophoresis is reserved a swimming lane and is done EB dyeing, detects the electrophoresis quality and determines the band position.Finish behind the about 7h of electrophoresis.With the glue taking-up, with the DEPC water wash for several times, put into 20 * SSC solution and soak 45min removal formaldehyde altogether 2 times.RNA in the gel is inhaled seal be transferred to the Hybond-N nylon membrane, finish after shifting about 14h.Behind sample hole site on the mark on the film, peel off, put into the rinsing of 6 * SSC solution, dry with gel.In UV-crosslinked instrument, make RNA crosslinked fixing then.

(2) Northern hybridization

Probe is taken from the cDNA recon that picking at random sieves again, and T7/SP6 amplifies and inserts sub-fragment, and the glass powder method reclaims each fragment, and the labelled with radioisotope probe carries out Northern hybridization.The hybridization of selecting for use is 65 ℃ with washing film temperature.Hybridization back radioautograph 7 days, the observation of developing a film.The 0.1%SDS solution rinsing Hybond membrane that the back usefulness of developing a film is boiled 1-3 time is washed (verifying by the radioactivity of surveying film) fully until probe.Then film and 18SrRNA probe are hybridized down in 68 ℃, wash 0.1 * SSC when washing film at last, radioautograph 2 days.

(3) electrophoretic separation of pcr amplification product, glue reclaim and the probe preparation

6 * the sample-loading buffer of PCR reaction product with 1/6 volume mixed, be splined on 1% sepharose, the 90V electrophoresis is 35 minutes in 1 * TAE damping fluid.After ethidium bromide (EB) dyeing, will contain the segmental gel of purpose and cut off and place 1.5ml eppendorf under UV 312nm, and add 3 times to the 6mol/L of gel volume NaI solution, 55 ℃ of water bath heat preservation 3-5min separate peptization.Add 5 μ l glass powder suspension liquids then, the vibration mixing is placed 5min on ice.13, the centrifugal 1min of 000g removes supernatant; Add the resuspended glass powder of lavation buffer solution 200 μ l, 13, the centrifugal 1min of 000g removes supernatant; Behind the repeated washing like this 2-3 times, remove most supernatant, 55 ℃ of water bath heat preservation 5min make the residual liquid volatilization.Add 15 μ l sterilized waters, the vibration mixing leaves standstill 10min, and 13, the centrifugal 1min of 000g gets supernatant and promptly gets required dna fragmentation.

Under 42 ℃ of conditions of Northern hybridization employing (5xSSC/5xDenhardt ' s/1%SDS/100ug/ml salmon sperm DNA/50% (V/V) methane amide), prehybridization 4hr adds the radiolabeled probe then, hybridization 16-24hr, wash film condition: 2xSSC/0.5%SDS, room temperature, 2 x 5min; 0.2xSSC/0.1%SDS, room temperature, 2 x 5min; 0.2xSSC/0.1%SDS, 42 ℃, 2 x 15min; 0.1xSSC/0.1%SDS, 68 ℃, 2 x 15min.

8, cDNA sequencing fragment and BLAST analyze

The automatic sequencing of pcr amplification product

The preceding operational manual extracting and purifying plasmid of order-checking according to Plasmid Purification Kit.Microbionation and cultural method are the same.Collect cell contained in the 4ml bacterium liquid in a 1.5ml centrifuge tube.Under the room temperature, every pipe adds the solution 1 that 250 μ l have comprised the RNA enzyme, and vibration mixing somatic cells adds 250 μ l solution 2 again, quick mixing, and room temperature is placed 3min.The solution 3 that adds the precooling of 350 μ l ice is afterwards put upside down centrifuge tube for several times, leaves standstill 5min on ice.Then 13, the centrifugal 10min of 000g is transferred to supernatant in another centrifuge tube that is with miniature filter post.13, the centrifugal 1min of 000g, this moment, plasmid was attached on the filter post.Discard the liquid in the sleeve pipe; Add 500 μ l solution 4 in the filter post, again with 13, the centrifugal 1min of 000g discards the liquid in the sleeve pipe; Add 700 μ l solution 5,13 in the filter post, the centrifugal 1min of 000g discards the liquid in the sleeve pipe; The centrifugal again filter post that once makes dries.Change a clean sleeve pipe, in the filter post, add 100 μ l sterilized waters, 13, the centrifugal 1min of 000g collects the solution in the sleeve pipe, promptly gets the plasmid of purifying.Electrophoresis is identified the purity and the concentration of plasmid.

Get 300ng plasmid and sequencing primer (T7 or SP6) and join in the 3 μ l Big Dye reaction mixtures, moisturizing to cumulative volume is 7.5 μ l, of short durationly puts into the PCR instrument after centrifugal, carries out sequencing reaction by following program: 96 ℃ of sex change 10s; Again by 96 ℃ of 5s, 50 ℃ of 10s, 60 ℃ of 4min carry out 25 circulations. and reaction finishes the back and adds 95% ethanol 30 μ l, and the vibration mixing places 30min on ice, and with 13, the centrifugal 20min of 000g removes supernatant under 4 ℃; Add 70% ethanol 100 μ l washing, with 13, the centrifugal 10min of 000g removes most supernatant under 4 ℃.Uncap under 4 ℃ and dry more than the 2h, add 2 μ l sample-loading buffer dissolution precipitations.95 ℃ of sex change 2min of elder generation before the last sample carry out nucleotide sequence with ABI Prism 377 automatic dna sequencers then and measure.

9, the isolation identification of full-length cDNA

(1) preparation of cDNA library Hybond membrane

Inoculation intestinal bacteria XLl-Blue MRF ' in the LB liquid nutrient medium that contains 50 μ g/ml tsiklomitsins, under 37 ℃, the 240rpm overnight incubation.Next day bacterium liquid is inoculated in the ratio of 1:100 and does not contain among the antibiotic 50ml liquid LB, under 37 ℃, 300rpm is cultured to bacterium liquid O.D. ₆₀₀=0.5,1000g is centrifugal, removes supernatant, adds the Adlerika re-suspended cell of 8ml 10mmol/L.

Get the recipient bacterium liquid 5ml for preparing and comprise at least one root cDNA library amount (2.7 * 10 ⁵Individual phage) λ ZAP Express mixes, and 37 ℃ of insulation 15min fully adsorb phage.Get 0.8% top-agar 9ml mixing of mixed solution 0.7ml and 48 ℃ of preheatings, be layered on rapidly on the 15cm LB flat board of 37 ℃ of preheatings.Bed board is 7 altogether.After treating that top-agar solidifies, flat board is inverted in 37 ℃ of overnight incubation.

Cover with dull and stereotyped back flat board is taken out Deng plaque, 4 ℃ make the planar surface hardening more than placing 2h down.Get a Hybond-N+ nylon membrane that is slightly less than flat board and be covered in planar surface, take off behind the 1min.Film put in sex change liquid (1.5MNaCl, 0.5M NaOH), neutralizer (1.5M NaCl, the Tris-Cl of 0.5M pH7.4) and the 2 * SSC solution successively handle 3min, 5min behind the 1min, places on the clean filter paper and dries.Putting into UV-crosslinked instrument (Bio-Rad company product) again carries out UV-crosslinked with the C3 program.

(2) cDNA clone's screening

The Hybond membrane for preparing is put in the prehybridization solution (containing 6 * SSC, 5 * Denhart ' s, 0.5%SDS, 100 μ g/ml denatured calf thymus dnas), and 68 ℃ of prehybridization 1-2h carry out the radio-labeling of probe simultaneously.

Getting the plasmid that has pcr amplified fragment for preparing in the experiment is template, restriction enzyme digestion, gel electrophoresis, and the recovery fragment is used for probe mark.Get 200ng and reclaim fragment, be inserted in cooled on ice in the boiling water bath behind the sex change 3min rapidly.The DNA of sex change is joined in the 50 μ l systems that contain following ingredients: dCTP, dGTP, dTTP (final concentration respectively is 20 μ mol/L), [α- ³²P] dATP (final concentration 333nmol/L, intensity of radioactivity 50 μ Ci), bovine serum albumin (final concentration 400mg/L), Klenow enzyme (final concentration 10 ⁵U/L).Do centrifugally behind the mixing slightly, react 1-2h under the room temperature.After labeled reactant is finished, add a little blue dextran, mixing.Do an easy Sephadex G-50 chromatography column with dropper simultaneously.Reaction solution is crossed post, collect blue color component.With the liquid boiling water bath sex change 5min that collects, place cooled on ice rapidly again, promptly get hybridization probe.

After prehybridization finished, the probe that mark is good joined in the prehybridization solution, hybridized 14h down for 68 ℃.After finishing hybridization solution is poured out preservation so that use in next round sieve storehouse.Hybond membrane is used 2 * SSC successively, 1 * SSC, and 0.5 * SSC (all containing 0.1% SDS) solution is in 60 ℃ of rinsings.Film is taken out, inhale with paper handkerchief and remove unnecessary liquid, again film is wrapped with preservative film, measure intensity of radioactivity.-70 ℃ of following radioautograph, according to radioactive power, the compressing tablet time at 24 hours to not waiting in a week.

After developing a film,, on flat board, find out the plaque of corresponding position, dig down, and be put in the centrifuge tube of the 1.5ml that contains 1ml SM solution and 40 μ l chloroforms with aseptic dropper according to the black splotch on the X-ray sheet.Vibration is broken up the back in 4 ℃ of preservations.Get an amount of phage suspension, carry out the two-wheeled screening again by the described method of preamble, until obtaining pure phage clone.

(3) cDNA clone's pBK-CMV plasmid cuts off

Inoculate intestinal bacteria XLOLR in the LB liquid nutrient medium that contains 50 μ g/ml tsiklomitsins, 37 ℃, the 240rpm overnight incubation.Next day bacterium liquid is inoculated in the ratio of 1:100 and does not contain among the antibiotic 50ml liquid LB, 37 ℃, 300rpm is cultured to bacterium liquid O.D. ₆₀₀=1.0, standby.

Single plaque suspension and 1 μ l ExAssist helper phage that 250-500 μ l is screened join 200 μ lXL1-Blue MRF ' (O.D. ₆₀₀=2.0) in, 37 ℃ of insulation 15min. add 3ml LB liquid nutrient medium, and in the shaking table 37 ℃, 240rpm cultivates 2-2.5h, and taking-up places 70 ℃ of water-bath 15min, and the centrifugal 5min of 4000g stays supernatant then.

100 μ l supernatant liquors are mixed 37 ℃ of insulation 15min with freshly prepd XLOLR recipient bacterium.Add 300 μ l liquid LB again, in the shaking table 37 ℃, 240rpm cultivates 45min.Take out, coat on the LB flat board that contains 50 μ g/ml kantlex, be inverted overnight incubation for 37 ℃.The bacterium colony that can grow on resistant panel promptly contains pBK-CMV plasmid (have cDNA and insert fragment).

(4) evaluation of cDNA positive colony and order-checking

Alkaline process extracting pBK-CMV plasmid, T3/T7 primer are made PCR and are identified the insertion clip size.To insert fragment and be inserted into pBlueScript II SK+ plasmid, and utilize the T3/T7 primer sequence that is positioned at pBlueScript II SK+ plasmid multiple clone site both sides to carry out automatic sequencing.

10, the screening of genomic library

Except that phage and recipient bacterium have changed into respectively λ EMBL 3 and the E.coli p2392, the method that screens gene clone from gene library is basic identical with the method in screening cDNA library.

11, the separation of 0sPIG-1 gene

Obtain 11 0sPIG gene clones with the aforesaid method screening.Wherein, phage and recipient bacterium are respectively λ EMBL 3 and E.coli p2392, and the positive colony that screens need not cut off as plasmid.

Increase separating the positive colony that obtains, to obtain enough phages.The competence for preparing recipient bacterium p2392 by above-mentioned method.Get 10 ⁵The positive λ EMBL3 phage of pfu mixes with the 0.1ml recipient bacterium, and 37 ℃ of absorption 15min behind adding 3ml 0.7% top-agar and the mixing, pour a fresh LB flat board into.Cultivate 6-8h for 37 ℃ and cover with flat board to plaque, adding 5ml SM solution places 4 ℃ of a few hours, intermittently shakes, and phage is leached.Sucking-off SM adds 1ml SM again on flat board; Flat board is tiltedly put 15min, with the SM and the primary merging of sucking-off.Add the 0.1ml chloroform in the phagocytosis body fluid of collecting, slight vibration with the centrifugal 10min of 4000g, is reclaimed supernatant in 4 ℃, adds 40 μ l chloroforms, 4 ℃ of preservations.

With low multiple infection method amplification phage, behind the glycerine gradient centrifugal purification, prepare phage DNA.Elder generation inoculates single bacterium colony of recipient bacterium p2392 in 50ml liquid LB, 37 ℃, 240rpm overnight incubation.Next day is according to the OD of bacterium liquid ₆₀₀Value is by 1 OD=8 * 10 ⁸Individual cell calculates bacterial concentration.Get 2 parts of bacterium liquid, every part contains 10 ¹⁰Individual bacterium, the centrifugal 10min of 4000g removes supernatant, adds the resuspended precipitation of 3ml SM.Add 5 * 10 respectively in two duplicate samples ⁷With 5 * 10 ⁸The recombinant phage of pfu, 37 ℃ the insulation 20min, or the vibration.Every duplicate samples is joined 250ml in the liquid LB of 37 ℃ of preheatings, 37 ℃, 300rpm are cultivated 8-12h again, until bacterial cultures near cracking fully.In bacterium liquid, add the 5ml chloroform again, after continuing to cultivate 10min culture is taken out.

After culture is cooled to room temperature, add pancreas DNase I and pancreas RNase enzyme (final concentration is 1 μ g/ml), digest 30min under the room temperature.Add solid sodium chloride and solid polyethylene glycol (PEG 6000) to final concentration and be respectively 1mol/L and 10%.After treating the solid dissolving, ice bath 1.5h makes the phage precipitation.With the centrifugal 10min of 11000g, abandon supernatant under 4 ℃, the phage precipitation is resuspended in (50mmol/L pH7.8 Tris-Cl, 10mmol/L MgS0 in the 10ml TM solution ₄)。Add the equal-volume chloroform in suspension, vibration 30s with the centrifugal 15min of 3000g, reclaims the water that contains phage under 4 ℃.Follow these steps to prepare the glycerine stepwise gradient:

I) the TM solution that 3ml is contained 40% glycerine adds excess of imports centrifuge tube bottom.

Ii) on 40% glycerine-TM solution, spread the TM solution that 4ml contains 5% glycerine carefully.

Iii) the phage suspension is layered on carefully 5% glycerine-TM solution above.

Iv) the remaining space of centrifuge tube is filled it up with TM solution.

Under 4 ℃, the super centrifugal 60min of 35000rpm.Abandon supernatant, add the resuspended precipitation of 1ml TM solution.Promptly get the recombinant phage of purifying.

In the phage suspension, add 5 μ g pancreas DNA enzymes, 1 μ g Pancreatic RNase, 37 ℃ of digestion 30min.EDTA solution 40 μ l, the Proteinase K 50 μ g, the 10%SDS solution 50 μ l that add 0.5mol/LpH8.0 again are incubated 1h in 56 ℃ behind the mixing.After Digestive system is cooled to room temperature, add isopyknic balance phenol (pH8.0), upset is mixing for several times.The centrifugal 5min of 3000g reclaims the upper strata water; Use the phenol of isopyknic 1:1 more respectively: the chloroform of chloroform and 24:1: primary isoamyl alcohol extracting water respectively once.The sodium acetate solution that adds the 3mol/L pH7.0 of 1/10 volume then, the dehydrated alcohol of 2 times of volumes, room temperature is placed 30min.With the centrifugal 10min of 13000g, abandon supernatant and add lml 70% washing with alcohol precipitation under 4 ℃; Again under 4 ℃ with the centrifugal 2min of 13000g, remove most supernatant.After the DNA precipitation drying at room temperature, add the TE damping fluid dissolving of 100 μ l pH7.5.

With multiple restriction enzymes such as SalI reorganization λ DNA is made restriction analysis, make up and insert segmental physical map.Simultaneously the DNA endonuclease bamhi in the running gel is transferred to Hybond-N ⁺Film is made Southern blot with the used probe of library screening and is analyzed, and determines the position of 0sPIG-1 gene in inserting fragment.Each endonuclease bamhi is inserted into pBlueScript II SK+ plasmid, makes up subclone.Check order with the T3/T7 primer, and the nucleotide sequence of each subclone is spliced, obtain 0sPIG-1cDNA (SEQ ID No.1).

12, the acquisition of 0sPIG-1 gene 5 ' upstream regulatory sequence

According to the sequence of rice genome database, designed two pairs of primers (SEQ ID No.5, SEQ ID No.6, SEQID No.7), amplify the promoter sequence (SEQ ID No.3, SEQ ID No.4) of 0sPIG-1 gene.

The segmental amplification of ATG upstream 2205bp:

F：5’GTTTCAAGTAAAGCATGTAGGG?3’

R：5’TGTGGAAGCAAGAGGTATTTAC3’

The PCR reaction conditions:

94℃， 5min

94℃ 46sec

52℃ 46sec

72℃ 1min30sec

Circulate 30 times

Extend 72 ℃ of 10min

The fragment that amplifies is reclaimed, and clone (T-Vector) transforms the LB/Amp enzyme and cuts evaluation, and order-checking shows result and the Genbank data consistent of surveying from two.

The segmental amplification of ATG upstream 1137bp:

F：5’GTTTCAAGTAAAGCATGTAGGG3’

R：5’CCACCTGTCATACACATACTGC3’

The PCR reaction conditions:

94℃， 5min

94℃ 46sec

52℃ 46sec

72℃1min 30sec

Circulate 30 times

Extend 72 ℃ of 10min

It is the same to reclaim, clone, transform, check order.

13, the structure and the transgenic research of the plant transgene carrier of band 0sPIG-1 promotor

Relatively have the restriction enzyme site on 0sPIG-1 gene upstream sequence T carrier and the double base transgene carrier pCAMBTA 1301 (containing gus reporter gene).Pick out the combination of suitable double digestion respectively, make that original CaMV 35S promoter can be excised fully on the carrier, and the purpose fragment after enzyme is cut there is identical sticky end with carrier segments.Use Nco I, EcoR I double digestion respectively, can obtain the upstream regulation and control orders (SEQ IDNo.3,4) of the 0sPIG-1 gene of the about 2.2kb of length, 1.1kb.

Enzyme is cut product 4 ℃ of following connections of b after gel electrophoresis reclaims and is spent the night.Coat ligation product transformed into escherichia coli TOP 10 competent cells on the LB flat board that has suitable microbiotic (kantlex or penbritin) next day, cultivates 14h down for 37 ℃.Choose single colony inoculation from flat board, 37 ℃ of following overnight incubation, alkaline process extracting plasmid promptly gets the transgene carrier after recombinating, and comprises the 0sPIG-1 upstream region of gene regulating and controlling sequence of two kinds of length respectively.

Choose fresh onion, in super clean bench, choose limb near the core, with the tear entocuticle of limb of tweezers, shiny surface is tiled in downwards on the MS culture medium flat plate that contains 1.5% agar, inductive experimental group wherein adds the allyl isothiazole (PBZ) of 100mg/L or contains the Whitfield's ointment (SA) of 200mg/L in the substratum.The Col wild-type Arabidopsis leaf of growing nearly January beats before the particle gun that the seedling from nutrition pot is cut, aquae destillata is cleaned, and expresses test as moment.When the paddy rice mature embryo is expressed test materials as gene moment, earlier with seed with 0.1% the mercuric chloride 4min that sterilizes; With the residual mercuric chloride of sterilized water flush away, after shelling, embryo is peeled with scalpel, again EMBRYO IN RICE was soaked in liquid MS medium 2 days.

Take by weighing 100mg bronze or tungsten powder (particle diameter 1.5-3.0 μ m) and put into the 1.5ml centrifuge tube, add the 1ml dehydrated alcohol, mixing fully vibrates; The centrifugal 1min of 13000g removes supernatant.With the resuspended precipitation of 1ml sterilized water, supersound process 1min with the centrifugal 1min of 13000g, removes supernatant again.Precipitation with absolute ethanol washing for several times after, be resuspended in the 1ml dehydrated alcohol.With bronze or tungsten powder suspension vibration mixing, draw 30 μ l, add transgene carrier (concentration is 1 μ g/ μ l) 60 μ l and 2.5mol/L calcium chloride solution 75 μ l, the vibration mixing.Add 0.1mol/L spermidine 30 μ l again, the vibration mixing.Ice bath 20min, during take out vibration frequently.The centrifugal 1min of 13000g abandons supernatant; Precipitation is resuspended in the 30 μ l dehydrated alcohols with washing with alcohol twice.

Before using particle gun to transform, with 75% ethanol particle gun (Bio-Rad company product) is carried out disinfection earlier.By the working specification that Bio-Rad company provides, the bronze or the tungsten powder (every ware 10 μ l bronze suspensions) that will have transgene carrier are squeezed in the plant tissue.The helium pressure of selecting for use is 1100kPa.

Onion epidermis after the conversion, Arabidopsis leaf and paddy rice mature embryo are cultivated after 1 day under 25 ℃, in the white light, place culture dish, add the X-Gluc staining fluid, 37 ℃ down dyeing observe the colour developing result after about 5 hours, formaldehyde solution through 3% is fixed, and takes pictures at microscopically.

37 ℃ of down dyeing after about 5 hours contain above-mentioned 0sPIG-1 upstream sequence and all can be by being observed visually blue spot through PBZ inductive experimental group, are the result of gus protein and its substrate-function of abduction delivering; And do not induce group not observe blue reaction product in any cell.This organizes presentation of results, and the regulation and control order of upstream 2.2kb, the 1.1kb of 0sPIG-1 gene all can the induction regulating controlling exogenous gene expression.

After the stable conversion, in Arabidopsis leaf and root, also observe above-mentioned abduction delivering effect.Abduction delivering effect in the paddy rice is similar to the above.

The sequence that the present invention relates to

The information of SEQ ID No:1

Length: 1749 bases

Type: nucleic acid

Chain: strand

Topological framework: linearity

Molecule type: cDNA

Sequence description: SEQ ID No:1

1?atggagccgc?cgaccagcca?cgtcaccaac?gcgttctccg?actcggacag?cgcgtccgtg

61?gaggaggggg?gcgccgacgc?ggacgccgac?gtggaggcgc?tccgccgcct?ctccgacaac

121?ctcgccgcgg?cgttccgctc?gcccgaggac?ttcgcgttcc?tcgccgacgc?gcgcatcgcc

181?gtcccgggcg?gcggcggcgg?cggcggcgac?ctgctggtgc?accgctgcgt?gctctccgcg

241?cggagcccct?tcctgcgcgg?cgtcttcgcg?cgccgcgccg?ccgccgccgc?aggcggcggc

301?ggcgaggatg?gcggcgagag?gctggagctc?cgggaactcc?tcggcggcgg?cggcgaggag

361?gtggaggtcg?ggtacgaggc?gctgcggctg?gtgctcgact?acctctacag?cggccgcgtc

421?ggcgacctgc?ccaaggcggc?gtgcctctgc?gtcgacgagg?actgcgccca?cgtcgggtgc

481?caccccgccg?tcgcgttcat?ggcgcaggtc?ctcttcgccg?cctccacctt?ccaggtcgcc

541?gagctcacca?acctcttcca?gcggcgtctc?cttgatgtcc?ttgataaggt?tgaggtagat

601?aaccttctat?tgatcttatc?tgttgccaac?ttatgcaaca?aatcttgcat?gaaactgctt

661?gaaagatgcc?ttgatatggt?agtccggtca?aaccttgaca?tgattactct?tgagaagtca

721?ttgcctccag?atgttatcaa?gcagattatt?gatgcacgcc?taagcctcgg?attaatttca

781?ccagaaaaca?agggatttcc?taacaaacat?gtgaggagga?tacacagagc?ccttgactct

841?gacgatgtag?agctagtcag?gatgctgctc?actgaaggac?agacaaatct?tgatgatgcg

901?tttgcactgc?actacgccgt?cgaacattgt?gactccaaaa?ttacaaccga?gcttttggat

961?ctcgcacttg?cagatgttaa?tcatagaaac?ccaagaggtt?atactgttct?tcacattgct

1021?gcgaggcgaa?gagagcctaa?aatcattgtc?tcccttttaa?ccaagggggc?tcggccagca

1081?gatgttacat?tcgatgggag?aaaagcggtt?caaatctcaa?aaagactaac?aaaacaaggg

1141?gattactttg?gggttaccga?agaaggaaaa?ccttctccaa?aagataggtt?atgtattgaa

1201?atactggagc?aagctgaaag?aagggaccca?caactcggag?aagcatcagt?ttctcttgca

1261?atggcaggtg?agagtctacg?aggaaggttg?ctgtatcttg?aaaaccgagt?tgctttggcg

1321?aggattatgt?ttccgatgga?ggcaagagta?gcaatggata?ttgctcaagt?ggatggaact

1381?ttggaattta?acctgggttc?tggtgcaaat?ccacctcctg?aaagacaacg?gacaactgtt

1441?gatctaaatg?aaagtccttt?cataatgaaa?gaagaacact?tagctcggat?gacggcactc

1501?tccaaaacag?tggagctcgg?gaaacgcttt?ttcccgcgat?gttcgaacgt?gctcgacaag

1561?atcatggatg?atgaaactga?tccggtttcc?ctcggaagag?acacgtccgc?ggagaagagg

1621?aagaggtttc?atgacctgca?ggatgttctt?cagaaggcat?tccacgagga?caaggaggag

1681?aatgacaggt?cggggctctc?gtcgtcgtcg?tcatcgacat?cgatcggggc?cattcgacca

1741?aggagatga

The information of SEQ ID No:2

Length: 2502 bases

Type: nucleic acid

Chain: strand

Topological framework: linearity

Molecule type: genomic dna

Sequence description: SEQ ID No:2

CAGGATGGCCTTGTTTCAAGTAAAGCATGTAGGGGACATTGTATTATGTGAAATGAATTAGTTTAGT

ATAGTTTAGCTAAGGACTGGGCCTCACACATGCCACTCCCTTCCAACTCCGTGCAAAGTTTGGAGC

AATGACAAGTGGATCCAACTGGTAGAGTCCATAGCCAAACACAATAAAATTATGGGTACACATCCA

AGGCGAAAAAGCAAGTCATTAATCTTTCTTCACATCGACGTGTAGATGTGATCTCTTCTTTGTCAAT

CTTTGTTTTTTCACTTTCTTTAATACGGGCAGCTTCGTTTTGCAATTTGGTCCTTTCAGTTCCTGGAA

AATATAGAGTAAACACTCCTGCGTGTGGTGAACTGGTGACAAGTGACAACTCCTTTTATCTCTTCTT

TAATTGGAGCTGTTTATTACTTTATTGTAAAACTAATATAAGTTAACTACTCCCACTATTTCATAATAT

AAAACATGGTCAAATTTGGTACAATCTCCAACACTAATGTTTAGCTTATAATTTCTCATATAAGGTTT

GTAGCAATCAAATTATAGACATATGAAAGTAAATTTAAATCTCAAACTAATGATATAATTCTTAGCAA

ATAAAATTCATTTCATATTATACTAAGTGTTGGTCAAATGTTTTAAATGTTGATTCTTGAAATACGTG

AGTATAATCTTGTATGAAAAGGATAGAGGAAGAAAATTAAGAAATGTTAACTCTTATGTACTGAGCT

AACTGTATATTCCATTCTTTAGTTTTTCTAAAAGTGTAAGTCCTATTTGTAGTCAATAAGTGCTAAATT

AAATTGTTAATTGGAACCCAAGAAGCCATTCTATTACTTCGTTGTATGTTCATTGGTTTTGGAGTATC

ACACAGTGAATAAATTAATTGCTTCTTAGTCTTGGTGAAAAGAAATAGATTTTAGACTTTTGGAAGG

AGGCAGTTCATGCTTCAAGGTAAATATATTAATTACATAGGTGAGAGGAAAAGAGAAAAATAATTA

GATGCACCCTCAGAGTAAGTTTAATAGTATAGCTTACTACTAACTCCAATTCATTTATAGCCAATCTA

GTAGTCAATTTATACAATAGTTGCCTACTATACTATTAATATATGGTCCCACCTGTCATACACATACTG

CGTCTTGTAGTCCGTACTGCAGCTAGCTACAAATCTGTAGCCCGCTGGTCTTCTCTCTTATCTTTTAT

CTAATTAAAATATACTTATAGCTGGCTAATAGTCTGCTATTGTACTTGCTCTCATAGCTAATATATTATA

TATGTTCGTATTAATACTACTTTATGATTGATTTGTAATTATTTTACTACTAGTATTAAATTTGCTCTTA

CTCCAGTTCATACTACTTCCTCTGTCCACCAATGCAAGAGATTTAAACTAAAAATTATCCATAAACA

TGTTTAGAGTGTATACAGCTTCACCGACCCACTGGTAGTTTAGTCATTTGGCTTTTCAGTAAGCACT

TGATTAATTAATTATTAATTACTATAAATTTGAAGATAAATTTATTTAATATTGTGAAACCTTTTATTTA

GAAAAACTAAAACACACTATTTAGATGTTTTGGAGTTTGTTAATAAAAACGAGGGAGTTATCATCCT

AATATGCAAAAATAAACTAAGCCTTAGGGGCATAACTTCAACCTTAAACTTTGCTAATAGCCTACTC

CTTTCATTATAAAATATACTAGTAGGTCTTTACTACAAAACAAACATATGATAAAAACATATTTAATG

TTAGATTTAATAAAACTAATTTAATATTTTAAATAGTACTAAATTATTCTATAAATTTGGTCAAACTTA

ACAAGTTTGACAAAAGAAAAGTTAAACGACTCATAATATGAAACATAGGAGTATAGGTTATTACAG

TTGAGAAGAAAATATCTGGGTGTCACATGAGAACTTGTTGAGGTGAGAGGCTAGGGTAAGATAAA

AAGAAATTTAAAAAGTGGATGAGGGAGGCTAGAGTATAACACATAGTATTATGTATTATGAATACTC

CTTCCATCCTAAAAAAGCTGACCTAGTTAGGGATAGAAGATAACATAGTACGATGAATATTCATGTC

TAGACTTGCTACGTTAGGTTGTGTTCCATCCTTATTTTATTTTTTTTATGAAGGGAATAATTTCTCTCG

GAAGAGAGGAGGTGTGTAAGCCATTATTTGTGTGGGAAGCAAGAGGTATTTACGTTTGTTGGCTTTC

ACGAGGCACCACCAATTGTGCATTTGTCAGTTACTCCAGTCTGGTCAACGAAGGAATGACCTTGTAA

AATCCCTAAATCTACAGGTGCAATGTGCAAAATTGCGGTTTGCACCTCACTCCTCGTTTTACTACTC

CATCCCTTTCGCCTTCGACTTCCTCGCGCCTTCCCACCAGCTCGGGCGGGAGGCCTCCTCCTCGCC

TCGCCTCGCCACGCCGCGCCGCGACGCGACGCGCCGTGGTCAGCTGGTCGCCGGTGCGGGTGCG

GGTGCGCA

The information of SEQ ID No:3

Length: 2205 bases

Type: nucleic acid

Chain: strand

Topological framework: linearity

Molecule type: genomic dna

Sequence description: SEQ ID No:3

GTTTCAAGTAAAGCATGTAGGGGGACATTGTATTATGTGAAATGAATTAGTTTAGTATAGTTTAGCTAA

GGACTGGGCCTCACACATGCCACTCCCTTCCAACTTGATTCTTGAAATACGTGAGTATAATCTTGTA

TGAAAAGGATAGAGGAAGAAAATTAAGAATCCGTGCAAAGTTTGGAGCAATGACAAGTGGATCCA

ACTGGTAGAGTCCATAGCCAAACACAATAAAATTATGGGTACACATCCAAGGCGAAAAAGCAAGT

CATTAATCTTTCTTCACATCGACGTGTAGATGTGATCTCTTCTTTGTCAATCTTTGTTTTTTCACTTTC

TTTAATACGGGCAGCTTCGTTTTGCAATTTGGTCCTTTCAGTTCCTGGAAAATATAGAGTAAACACT

CCTGCGTGTGGTGAACTGGTGACAAGTGACAACTCCTTTTATCTCTTCTTTAATTGGAGCTGTTTAT

TACTTTATTGTAAAACTAATATAAGTTAACTACTCCCACTATTTCATAATATAAAACATGGTCAAATTT

GGTACAATCTCCAACACTAATGTTTAGCTTATAATTTCTCATATAAGGTTTGTAGCAATCAAATTATA

GACATATGAAAGTAAATTTAAATCTCAAACTAATGATATAATTCTTAGCAAATAAAATTCATTTCATA

TTTATACTAAGTGTTGGTCAAATGTTTTAAATGATGTTAACTCTTATGTACTGAGCTAACTGTATATCC

ATTCTTTAGTTTTTCTAAAAGTGTAAGTCCTATTTGTAGTCAATAAGTGCTAAATTAAATTGTTAATT

GGAACCCAAGAAGCCATTCTATTACTTCGTTGTATGTTCATTGGTTTTGGAGTATCACACAGTGAAT

AAATTAATTGCTTCTTAGTCTTGGTGAAAAGAAATAGATTTTAGACTTTTGGAAGGAGGCAGTTCAT

GCTTCAAGGTAAATATATTAATTACATAGGTGAGAGGAAAAGAGAAAAATAATTAGATGCACCCTC

AGAGTAAGTTTAATAGTATAGCTTACTACTAACTCCAATTCATTTATAGCCAATCTAGTAGTCAATTTA

TACAATAGTTGCCTACTATACTATTAATATATGGTCCCACCTGTCATACACATACTGCGTCTTGTAGTC

CGTACTGCAGCTAGCTACAAATCTGTAGCCCGCTGGTCTTCTCTCTTATCTTTTATCTAATTAAAATAT

ACTTATAGCTGGCTAATAGTCTGCTATTGTACTTGCTCTCATAGCTAATATATTATATATGTTCGTATTA

ATACTACTTTATGATTGATTTGTAATTATTTTACTACTAGTATTAAATTTGCTCTTACTCCAGTTCATAC

TACTTCCTCTGTCCACCAATGCAAGAGATTTAAACTAAAAATTATCCATAAACATGTTTAGAGTGTAT

ACAGCTTCACCGACCCACTGGTAGTTTAGTCATTTGGCTTTTCAGTAAGCACTTGATTAATTAATTAT

TAATTACTATAAATTTGAAGATAAATTTATTTAATATTGTGAAACCTTTTATTTAGAAAAACTAAAAC

ACACTATTTAGATGTTTTGGAGTTTGTTAATAAAAACGAGGGAGTTATCATCCTAATATGCAAAAAT

AAACTAAGCCTTAGGGGCATAACTTCAACCTTAAACTTTGCTAATAGCCTACTCCTTTCATTATAAA

ATATACTAGTAGGTCTTTACTACAAAACAAACATATGATAAAAACATATTTAATGTTAGATTTAATAA

AACTAATTTAATATTTTAAATAGTACTAAATTATTCTATAAATTTGGTCAAACTTAACAAGTTTGACA

AAAGAAAAGTTAAACGACTCATAATATGAAACATAGGAGTATAGGTTATTACAGTTGAGAAGAAAA

TATCTGGGTGTCACATGAGAACTTGTTGAGGTGAGAGGCTAGGGTAAGATAAAAAGAAATTTAAA

AAGTGGATGAGGGAGGCTAGAGTATAACACATAGTATTATGTATTATGAATACTCCTTCCATCCTAAA

AAAGCTGACCTAGTTAGGGATAGAAGATAACATAGTACGATGAATATTCATGTCTAGACTTGCTACG

TTAGGTTGTGTTCCATCCTTATTTTATTTTTTTTATGAAGGGAATAATTTCTCTCGGAAGAGAGGAGG

TGTGTAAGCCATTATTTGTGTGGAAGCAAGAGGTATTTAC

The information of SEQ ID No:4

Length: 1137 bases

Type: nucleic acid

Chain: strand

Topological framework: linearity

Molecule type: genomic dna

Sequence description: SEQ ID No:4

GTTTCAAGTAAAGCATGTAGGGGACATTGTATTATGTGAAATGAATTAGTTTAGTATAGTTTAGCTAAGGACTGGGCCTCACACATGCCACTCCCTTCCAACTTGATTCTTGAAATACGTGAGTATAATCTTGTATGAAAAGGATAGAGGAAGAAAATTAAGAATCCGTGCAAAGTTTGGAGCAATGACAAGTGGATCCAACTGGTAGAGTCCATAGCCAAACACAATAAAATTATGGGTACACATCCAAGGCGAAAAAGCAAGTCATTAATCTTTCTTCACATCGACGTGTAGATGTGATCTCTTCTTTGTCAATCTTTGTTTTTTCACTTTCTTTAATACGGGCAGCTTCGTTTTGCAATTTGGTCCTTTCAGTTCCTGGAAAATATAGAGTAAACACTCCTGCGTGTGGTGAACTGGTGACAAGTGACAACTCCTTTTATCTCTTCTTTAATTGGAGCTGTTTATTACTTTATTGTAAAACTAATATAAGTTAACTACTCCCACTATTTCATAATATAAAACATGGTCAAATTTGGTACAATCTCCAACACTAATGTTTAGCTTATAATTTCTCATATAAGGTTTGTAGCAATCAAATTATAGACATATGAAAGTAAATTTAAATCTCAAACTAATGATATATCTTAGCAAATAAAATTCATTTCATATTATACTAAGTGTTGGTCAAATGTTTTAAATGATGTTAACTCTTATGTACTGAGCTAACTGTATATTCCATTCTTTAGTTTTTCTAAAAGTGTAAGTCCTATTTGTAGTCAATAAGTGCTAAATTAAATTGTTAATTGGAACCCAAGAAGCCATTCTATTACTTCGTTGTATGTTCATTGGTTTTGGAGTATCACACAGTGAATAAATTAATTGCTTCTTAGTCTTGGTGAAAAGAAATAGATTTTAGACTTTTGGAAGGAGGCAGTTCATGCTTCAAGGTAAATATATTAATTACATAGGTGAGAGGAAAAGAGAAAAATAATTAGATGCACCCTCAGAGTAAGTTTAATAGTATAGCTTACTACTAACTCCAATTCATTTTATAGCCAATCTAGTAGTCAATTTATACAATAGTTGCCTACTATACTATTAATATATGGTCCCACCTGTCATACACATACTGC

The information of SEQ ID No:5

Length: 22 bases

Type: nucleic acid

Chain: strand

Topological framework: linearity

Molecule type: oligonucleotide

Sequence description: SEQ ID No:5

F：5′GTTTCAAGTAAAGCATGTAGGG?3′

The information of SEQ ID No:6

Length: 22 bases

Type: nucleic acid

Chain: strand

Topological framework: linearity

Molecule type: oligonucleotide

Sequence description: SEQ ID No:6

R：5’TGTGGAAGCAAGAGGTATTTAC?3’

The information of SEQ ID No:7

Length: 22 bases

Type: nucleic acid

Chain: strand

Topological framework: linearity

Molecule type: oligonucleotide

Sequence description: SEQ ID No:7

R：5’CCACCTGTCATACACATACTGC3’

Claims (1)

1, a kind of paddy rice systemic acquired resistance inductor inductive promotor that is subjected to is characterized in that the nucleotides sequence of described promotor is classified SEQ ID.NO.3 or SEQ ID.NO.4 as.