CN102220325A - Method for preparing cabbage type rape BnPABP3 promoter and application thereof - Google Patents

Abstract

The invention discloses a method for preparing a cabbage type rape BnPABP3 promoter (PBnPABP3) and the application thereof. The method comprises the following steps of: cloning PBnPABP3 sequence by utilizing the genome walking method, extracting genome DNA by utilizing the SDS cracking method, carrying out enzyme digestion on DNA by respectively using endonuclease DraI, EcoRV, PvuII and StuI in different systems, carrying out the first round of PCR amplification by adopting the product as a template after joint segments are connected with the product, and carrying out the second round of PCR amplification by adopting the 50 times diluent of PCR products obtained in the first round as a template so as to obtain the PBnPABP3. The PBnPABP3 is applied to anther and pollen grains of plant. The promoter has the function of driving exogenous gene expression, the expression parts of the promoter are in the anther and pollen grains of plant, and the promoter has the application potentiality in the aspects of improving the safety of rape edible oil as well as the quality of crops, artificially creating sterile line and restorer line, enriching germ plasm resources, and the like.

Description

The preparation method and the application thereof of swede type rape BnPABP3 promotor

Technical field

The present invention relates to plant genetic engineering and biological technical field.Be specifically related to a kind of swede type rape BnPABP3 promotor (called after P _BnPABP3, below identical), also relate to a kind of preparation method of swede type rape BnPABP3 promotor simultaneously.The invention still further relates to the carrier that contains this promotor or its homologous nucleotide sequence and utilize the application of this promotor in rape and other plant genetic engineering with relating to.

Background technology

Plant promoter plays keying action in the expression of gene regulation and control.Gene expression regulation is a result of various factor comprehensive action.Generally according to the sequencing of an incident, the regulation and control of gene are divided into transcriptional level control, translation skill regulation and control and the regulation and control of protein level of processing etc.The protein of genes encoding and RNA and secondary metabolite thereof are of crucial importance for the whole vital movement of keeping organism.The mistake of any gene expression regulation all can cause serious consequence to life.Therefore, the mechanism research for gene expression regulation is the focus of molecular biology research always.The regulation and control of transcriptional level are the most important.Promotor is the critical elements of transcriptional level control, also is an important component part of gene engineering expression carrier.To a certain extent, promotor has determined the space-time order and the expression intensity of genetic expression.So the function sequence of research promotor has very important significance for gene expression regulation mechanism and day by day sophisticated plant genetic engineering.

Promotor is making up and can play a key effect in the process of high level expression heterogenous expression carrier, and what it had determined foreign gene transcribes efficient and expression of gene level.The used promotor of plant transgene breeding can be divided into composing type and Idiotype two classes.The foreign gene that constitutive promoter drives is stably express in all developmental stages of transfer-gen plant and tissue.Conversion to many dicotyledonss, usually all use the 35S promoter that contains cauliflower mosaic virus (CaMV) or the plasmid vector of nopaline synthetic enzyme no promotor, and the most frequently used in monocotyledons transforms be to contain rice actin Act promotor, the plasmid vector of corn ubiquitin Ubi promotor and 35S promoter (Guan Liying etc., the effective expression of foreign gene and safety evaluation thereof in the transgenic plant.Capital Normal University's journal.2002，23(2)：52-56)。But many times foreign gene continuing in recipient plant efficiently expresses the waste that not only causes the energy in the organism, and the expression in a organized way might have toxic action to plant itself, even cause transgenosis safety problem (Jia S-R.Environment and food biosafty assessment of transgenic plants.Advanced of Bioengineer.1997,17 (6): 37-42; Morris S H, Adley C.C.Irish public perceptions and attitudes to modern biotechnology:an overview with a focus on GM foods.Trends in Biotechnology, 2001,19 (2): 43-48).Therefore, the research of inducible promoter and tissue-specific promoter and use the person's that is subjected to the breeding work day by day attention.The inducible promoter of identifying in transgenic plant comprises heat-inducible promoter, derives from (Guan Liying etc., the effective expression of foreign gene and the safety evaluations thereof in the transgenic plant such as inducible promoter of spinach nitrate reductase.Capital Normal University's journal.2002，23(2)：52-56)。But the application of inducible promoter also has certain limitation, and the external condition that recipient plant is carried out is handled, and as heat shock, HORMONE TREATMENT etc. may cause a series of biochemical reactions in the organism and be unfavorable for the normal growth of plant.And be used as in the chemical regulation system inductor Methylprednisone acetate (dex, dexamethasone), estradiol (estradiol) and tsiklomitsin (tetracycline) be all harmful to ecotope, should not be used for production practice.And the tissue-specific promoter of itself just can avoid this problem in the use plant materials.Obviously, the tissue specific expression of foreign gene will effectively improve the biological safety of genetically modified crops.Obtained great success in recent years in this respect.Specific expressed all kinds of promotors constantly obtain research (Song Yang etc., the research of plant tissue specificity promoter in different tissues.The biotechnology circular.2007，(4)：21-24)。

Rape is extensively planted in the Yangtze valley as the main oil crops of China, and national economy is had material impact.Along with the maturation of transgenic technology, transgene rape will inevitably face the public opinion of transgenosis security risk.Being used in the Semen Brassicae campestris fully the expression that expression promoter not starts goal gene is a feasible method that addresses this problem.Reach and both improve rape each side quality, do not cause the purpose of edible oil security risk again.

Therefore, the present invention has developed a swede type rape endogenesis promoter.Show that by fluorescence quantitative PCR detection the native gene of this promoters driven a large amount in the root of plant, stem, blade, bud, angle fruit expresses.Gene a large amount in root, stem, blade, bud and angle pericarp of the expression characteristic proof promoters driven by examining report gene GUS is expressed and is not expressed in the seed.Our result is indicating that the promotor of this gene has suitable application prospect in transgenic plant.

Summary of the invention

The objective of the invention is to be to provide a kind of swede type rape P _BnPABP3Promotor, the spatial and temporal expression pattern of this promotor can be used for studying the expression of gene form, advantage is, derive from plant endogenous tissue-specific promoter and can accurately locate the gene regulated and control, the driving purposes gene was expressed in particular organization or the period of transgenic plant, avoid causing the waste of plant self energy and material, improve the expression efficiency of foreign gene in transgenic plant, limit its expressive site.Can be applicable to the genetically engineered research of plant and seed with rape safety transgenic research.

Another object of the present invention is to be to provide a kind of swede type rape P _BnPABP3The preparation method of promotor.This method obtains swede type rape P by the swede type rape genome is carried out genomic walking _BnPABP3Sequence.Its advantage is simple to operate, and the result is reliable and stable.

A further object of the present invention is to be to provide a kind of recombinant vectors that plant efficient is expressed promotor that contains, and it contains described promotor nucleotide sequence.This carrier size is fit to, easy and conversion in plant, and the marker gene GUS expression intensity height that is had detects easily.Can obtain the Arabidopis thaliana transfer-gen plant that gus gene efficiently expresses by this carrier arabidopsis thaliana transformation in plant.

A further object of the invention is to be to provide a kind of swede type rape P _BnPABP3The application of promotor in flower pesticide, pollen granule.P _BnPABP3Function can reflect the function of rape BnPABP3 gene promptly in growth course, to have critical function; Under the driving of this promotor, goal gene is meticulous expression in the flower pesticide of plant, pollen granule mainly, and does not express fully in the seed.This promotor with tissue specific expression is created plant in genetically engineered such as sterile line, manual creation germ plasm resource and the transgenosis safety (edible, pollen drift) has using value.

In order to realize above-mentioned purpose, the present invention adopts following technical scheme:

In order to obtain the present invention, the contriver has carried out deeply and comprehensively research the genes involved in the rape growth course, found that a kind of new promotor.The native gene of this promoters driven efficiently expresses in the flower pesticide of plant, pollen granule.

According to an aspect of the present invention, above-mentioned purpose can realize by a kind of promotor is provided, described promotor can specificity drives gene and efficiently expresses in plant, described promotor contain SEQ ID No.1 nucleotide sequence or with SEQ ID No.1 homologous nucleotide sequence in fact.

According to another aspect of the present invention, above-mentioned purpose can realize by the recombinant vectors that the nucleotide sequence that contains described promotor is provided.

According to another aspect of the present invention, above-mentioned purpose can realize by providing with described recombinant vectors microorganism transformed.

According to another aspect of the present invention, above-mentioned purpose can realize by providing with the transgenic plant of described microbial transformation.

1, a kind of swede type rape promotor P _BnPABP3The preparation method, the steps include:

1.1P _BnPABP3The expression pattern of the native gene that drives:

The used rape of the present invention is swede type rape (Brassica napus L.).Be seeded in the land for growing field crops for the examination material, normal field management.

The plant that grows under the grown in field condition is got root, stem, leaf, bud, and angle every kind of material of fruit is got three repetitions at least, and each repeats at least one strain, and the sampling back is positioned in the liquid nitrogen-80 ℃ of preservations rapidly with the masking foil parcel.The extraction of RNA is carried out in the requirement that utilizes Trirol to extract test kit.

Quantitative real time PCR Instrument is RT ^TM-Cycler (Boao Biological Co., Ltd) adopts rape Actin as internal standard gene (accession number AF111812), and the Actin gene primer is 5 '-CTGGAATTGCTGACCGTATGAG-3 ' and 5 '-ATCTGTTGGAAAGTGCTGAGGG-3 '.P _BnPABP3The native gene primer that drives is 5 '-GGGAAGATGATAGGAAGGAAA-3 ' and 5 '-CTGGTGCTCTAATCTGTGAAAA-3 '.

Quantitative fluorescent PCR reacts every group of experiment and all finishes three biology repetitions, and each biology repeats to do at least three technology and repeats.Detect P respectively _BnPABP3The expression of the native gene that drives in rape tissue (root, stem, leaf, flower, angle fruit).

Calculate the relative expression quantity of gene with comparing Ct method (Δ Δ Ct).By 2 ^{-Δ Δ Ct}Relative expression quantity and systematic error (Kenneth J Livak.Thomas D Schmittgen.2001, the Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2 of estimation goal gene ^{-Δ Δ C}TMethod.METHODS 25,402-408).When calculating relative expression quantity, be reference with the sample of bud, be about to its value and convert 1 (standard value) to, other sample again with its relatively, obtain relative expression's value.

1.2 genomic walking clone P _BnPABP3Sequence:

Utilize SDS cracking process (J. Sa nurse Brooker .D.W. Russell work, Huang Peitang etc. translate molecular cloning test guide (third edition) Science Press) the extraction genomic dna, according to the genomic walking test kit (available from Clontech company, product code name Cat.No.638904) schedule of operation is carried out genomic walking.Concrete steps are: extract genomic dna 25 μ L (0.1 μ g/ μ L), cut with endonuclease Dra I, EcoR V, PvuII and Stu I enzyme respectively, add joint behind the purifying and form four different genomic dna storehouses, be used as genomic walking first round pcr template first, increase according to goal gene conserved sequence design Auele Specific Primer GSP1 (table 2) and genomic walking test kit (available from Clontech company, product code name Cat.No.638904) interior upstream joints primer AP1 (table 2).Second to take turns PCR be template with 50 times of diluents (water diluent) of first round PCR product, increases with the Auele Specific Primer GSP2 (table 2) and the joint primer AP2 (table 2) of quadrat method design, carries out second subsequently and take turns genomic walking.All PCR reactions are 50 μ L amplification systems: template 1 μ L, and dNTPs 0.2mM, primer 0.5mM, LATaq enzyme 1.25 units, 10 * LA-PCRbuffer (contains MgCl ₂) 5 μ L, moisturizing to 50 μ L.Reaction conditions is: 94 ℃ of pre-sex change 1min; 98 ℃ of 10s, 7 circulations of 72 ℃ of 6min; 98 ℃ of 10s, 33 circulations of 67 ℃ of 6min; 72 ℃ are extended 10min.The PCR product detects through 1.0% (mass volume ratio) agarose gel electrophoresis, gel reclaims test kit (available from root biochemical technology Beijing, sky company limited, below identical) after purifying reclaims, be connected to pMD18-T carrier (available from TaKaRa company, below identical), transform the gold bacterial strain (available from the precious biotechnology in Dalian company limited, below identical) competent cell, picking positive colony, enzyme are cut checking back order-checking, obtain the flanking sequence of goal gene upstream, this sequence comprises P _BnPABP3The initiator codon of the native gene that drives is to the promoter sequence of the section between the GSP2 and this gene.According to the sequence that obtains, the segmental primer P of design amplification promoter region _BnPABP3S:5 '-CAGAAGCTT (HindIII) AATTAAGAGAGAGAGAGAGAGAGAGAGAG-3 ' and P _BnPABP3A:5 '-GACATCTAGA (XbalI) GCTCGTGCGTTTACCTTTTTAGAGAA-3 ' is a template with the genomic dna, carries out pcr amplification.5 of all primers ' end contains Hind III restriction enzyme site, and 3 ' end contains Xba I restriction enzyme site.Reaction system is that 25 μ L include: 1 * PCR buffer, and MgCI 1.5mmol/L, dNTP0.2mmol/L (every liter of mmole), primer concentration are 0.5mol/L, Pfu enzyme 1.5 units, the about 100ng of template is provided with loop parameter as the case may be.(mass volume ratio, below identical) sepharose detects the PCR product through 1.0%, and gel reclaims test kit and reclaims each purpose deletion fragment.By the deletion fragment of each recovery: carrier (the 0.3pmol deletion fragment: the 0.1pmol carrier segments)=3: 1 mixed sample, add T4DNA ligase enzyme 5 units, 1 * reaction buffer, sterilized water replenish volume to 25ml, 16 ℃ of ligations of spending the night.(J. Sa nurse Brooker .D.W. Russell work, Huang Peitang etc. translate molecular cloning test guide (third edition) Science Press to freeze-thaw method transformed into escherichia coli gold bacterium, 96-99) in the competent cell.(it is as follows to fill a prescription: take by weighing 10 gram Tryptoness respectively, 5 gram yeast extracts and 10 restrain sodium-chlor, and 8 gram agar are dissolved in the distilled water successively, and constant volume is in 1000 milliliters to coat the LB solid medium that contains penbritin 50 μ g/mL.Be sub-packed in 500 milliliters of triangular flasks, 121 ℃, autoclave sterilization is 15 minutes under 6.859 * 104Pa.4 ℃ of refrigerations are standby) on the flat board, 37 ℃ of overnight incubation, respectively select three of hickies, (reaction system is that 25 μ L include: 1 * PCR buffer. to do bacterium colony PCR detection, MgCI 1.5mmol/L, dNTP 0.2mmol/L (every liter of mmole), primer concentration is 0.5mol/L, Pfu enzyme 1.5 units, the a small amount of bacterial plaque of toothpick picking with sterilization is done masterplate, loop parameter is set as the case may be), positive recombinant is inoculated in the liquid LB substratum that contains penbritin 50 μ g/mL, and (it is as follows to fill a prescription: take by weighing 10 gram Tryptoness respectively, 5 gram yeast extracts and 10 gram sodium-chlor are dissolved in the distilled water, and constant volume is in 1000 milliliters.Be sub-packed in 500 milliliters of triangular flasks, 121 ℃, autoclave sterilization is 15 minutes under 6.859 * 104Pa.4 ℃ of refrigerations are standby), 37 ℃ of following 200r/min shaking culture are spent the night, (J. Sa nurse Brooker .D.W. Russell is outstanding for alkaline process in a small amount, Huang Peitang etc. translate molecular cloning test guide (third edition) Science Press) the extraction plasmid, Hind III/Xba I digested plasmid 1 μ g, 0.8% (mass volume ratio) agarose gel electrophoresis detects.Detect correct positive recombinant clone, called after pMD18-P _BnPABP3(the purpose fragment is connected into the pMD18-T vector construction forms, below identical) in order to ensure the sequence information of promotor in the carrier, is primer (M13 F5 '-AGCGGATAACAATTTCACACAGGA-3 ' with M13F/M13R; M13R5 '-GTAAAACGACGGCCAGT-3 '), with pMD18-P _BnPABP3Carry out sequencing, analytical results has obtained P _BnPABP3Its sequence is a nucleotide sequence shown in the SEQ ID NO:1.

1.3 promoter sequence bioinformatic analysis:

Institute's cloned sequence is carried out the homology comparison with BLASTN (http://www..ncbi.nlm.nih.gov/BLAST).Core promoter element and Upstream cis acting promotor forecasting software http://www.fruitfly.org/seq_tools/promoter.html and PLACE (Higo et al., Plant cis-acting regulatory DNA elements (PLACE) database (J) .Nucleic Acids Research.1999,27:297～300) http://www.dna.affrc.go.jp/PLACE/ predicts.Obtain possible core promoter sequence and upstream promoter element.

2, a kind of swede type rape promotor P _BnPABP3In the flower pesticide of transfer-gen plant, the application in the pollen granule, the steps include:

2.1P _BnPABP3The conversion of the structure of plant expression vector and agrobacterium tumefaciens bacterial strain EHA105 (purchasing still identical below the bio tech ltd) in Shanghai, Shanghai:

The recombinant vectors that makes up is that the 35S promoter on the plasmid pBI121 (available from TaKaRa company) is obtained P with clone in the technical scheme 1 _BnPABP3Fragment is replaced.For finishing this purpose, at first use Xba I/Hind III double digestion cloning vector pMD18-P _BnPABP3Promoter fragment, cut pBI121 (Chen with Xba I/Hind III enzyme simultaneously, P.Y., Wang, C.K., Soong, S.C.To, K.Y.Complete sequence of the binary vector pBI121 and its application in cloning T-DNA insertion from transgenic plants.Mol.Breed.11,287-293) plasmid.Endonuclease reaction carries out in 37 degree incubators, after about 4-6 hour, with 1% (mass volume ratio.Below identical) agarose gel electrophoresis detects.With cloning vector pMD18-P _BnPABP3The big fragment that small segment that enzyme downcuts and pBI121 (front is stated) enzyme downcut reclaims test kit (front is stated) with dna gel and reclaims.Press pMD18-P _BnPABP3The big fragment that small segment that enzyme downcuts and pBI121 (front is stated) enzyme downcut (the little mistake fragment of 150ng: the big fragment of 50ng)=3: 1 ratio (molar concentration rate) biased sample, add T4 dna ligase 5 units, 10 * reaction buffer, sterilized water replenishes volume to 20 μ L, and 16 ℃ of connections are spent the night.After the conversion, on the solid LB culture medium flat plate that contains kantlex (50 μ g/mL), screen, choose spot and be bacterium colony PCR, and the upgrading grain, cut the correct recombinant plasmid called after pBI-P of checking through enzyme _BnPABP3(step is as follows: 1: get 0.2ml competence Agrobacterium, slowly melt in frozen water to utilize freeze-thaw method.2: add about 2 μ g recombinant plasmid dnas, mixing behind the ice bath 30min, drops into liquid nitrogen flash freezer 1min gently, and 37 ℃ of water-bath 5min melt cell then.3: add 800 μ l and do not contain microbiotic YEP liquid nutrient medium, 28 ℃ of jogs are cultivated 4-5h.4:12000rpm, 30s removes supernatant, and cell is resuspended in the 0.2mlYEP substratum.5: culture is uniformly coated on contains Rif (50mg/L), on the agar plate of Str (50mg/L) and Kan (50mg/L), cultivated 2 days for 28 ℃, treat to occur on the flat board to choose bacterium behind the transformant and detect) with pBI-P _BnPABP3Change agrobacterium tumefaciens EHA105 (available from the precious biotinylated biomolecule in Dalian Products Co., Ltd, below identical) over to, screen, choose spot, bacterium colony PCR detection validation with kantlex (50 μ g/mL) and the two resistant panel of Rifampin (50 μ g/mL).

2.2P _BnPABP3Functional analysis:

2.2.1P _BnPABP3Plant expression vector pBI-P _BnPABP3Genetic transformation in Arabidopis thaliana and transfer-gen plant screening:

Method in the reference literature carry out Arabidopis thaliana transform (Zhang X.R.et al.Agrobacterium-mediated transformation of Arabidopsis thaliana using the floral dip method.Nature, 2006,1:1-6).Preparation contains agrobacterium tumefaciens EHA105 (front is stated) the bacterium liquid that builds carrier, changes in the LB liquid nutrient medium that contains kantlex 50 μ g/ml, Rifampin 50 μ g/ml 28 ℃ of incubated overnight over to the day before yesterday in conversion.Second day, the light absorption value with ultraviolet spectrophotometer (SPEKOL 1300) detection bacterium liquid under the 276nm nano wave length took out when the light absorption value of bacterium liquid reaches between 1.6-2.0.Room temperature (20-25 ℃, below identical) with the centrifugal 10min of 4000g, is abandoned supernatant, and precipitation is suspended in isopyknic 5% sucrose (mass volume ratio).The sucrose solution of muddiness is poured in the big culture dish, added the Silwet 1-77 that final concentration is 0.02% (volume ratio) (available from the Five continents, Beijing unit industry science and trade center, below identical) before transforming.The whole inflorescence of Arabidopis thaliana to be transformed being immersed in the sucrose gently, silent several 15 seconds, take out plant behind the mixing.Plant after the conversion is wrapped with a black plastic bag, is placed on the growth case and cultivates.Plastics bag was opened in second day, cultivate in the place that is placed on light intensity.Every the conversion that tries again in a week.Cultivate and gathered in the crops seed in about one month, seed under incubator or daylight dry 3-5 days.The T0 that transforms results is distinguished surface sterilization 3 minutes and 10 minutes for seed with the mercuric chloride of 70% (volume ratio) alcohol and 0.01% (mass ratio), with distilled water wash several (5～7 times), blow and beat MS solid screening culture medium (MS macroelement mother liquor 100ml then equably then; MS trace element mother liquor 10ml; The organic mother liquor 10ml of MS; MS molysite 10ml; Inositol 10ml; Sucrose 30g; Transfer PH to 5.8 with 1M NaOH, the 12g agar powder is settled to 1L, and high pressure 121 degree sterilization backs are standby.Add the 8g agar powder and can be configured to solid medium.Various mother liquor prescriptions see Table 1) surface.4 ℃ vernalization 4-6 days, put into constant incubator (photoperiod 16 (daytime)/8 (dark) hour, temperature: 22 ℃ of daytimes, 20 ℃ of dark cycles) and cultivate.Screen positive seedling according to peculiar kalamycin resistance on the expression vector.Blade is long when enough big or small (3-4 leaf phase), get a little green seedling leaf, extract DNA, carry out the PCR positive detection (reaction system is that 25 μ L include: 1 * PCR buffer., MgCI 1.5mmol/L, dNTP 0.2mmol/L (every liter of mmole), primer concentration are 0.5mol/L, Pfu enzyme 1.5 units, the about 100ng of template is provided with loop parameter as the case may be), the result shows and has obtained the transgenic positive seedling.

Table 1MS substratum mother liquor prescription

2.2.2P _BnPABP3Functional analysis:

Use P _BnPABP3Replace the 35S promoter sequence on pBI121 (front the is stated) plasmid, form pBI-P _BnPABP3The recombinant plant expression vector, gus gene wherein is subjected to P _BnPABP3Regulation and control.Utilize the inflorescence infestation method arabidopsis thaliana transformation of agrobacterium tumefaciens EHA105 (front is stated) mediation.T1 obtains positive plant (front is stated) for utilizing kalamycin resistance and PCR to detect screening.

With PCR checking be male T1 for the transfer-gen plant seed at MS (front is stated) substratum upper seeding wheel, in the growth case, sprout after 4 ℃ of vernalization, the back of emerging began sampling dyeing in 5-7 days.Dyeing course is as follows: sample is immersed in GUS dye liquor (X-gluc 0.5mg/mL, phosphoric acid buffer 50mmol/L, each 0.5mmol/L of the Tripotassium iron hexacyanide and yellow prussiate of potash, EDTA 10mmol/L, Triton-x-100 0.001% (volume ratio), in the methyl alcohol 20% (volume ratio), vacuum suction 5 minutes, 37 ℃ are spent the night.Decoloured with alcohol-acetate (volume ratio is 1: 1) in second day, and bleached until blade, use distilled water rinsing (5～7 times) for several times afterwards, Stereo microscope (OLYMPUS SZX16) is taken pictures.Get the whole plant of different time sections seedling stage; Reproductive stage, blade are got tender leaf and mature leaf; The inflorescence of flower that flower took away and the bud of not opening; The angle fruit of different times is really got at the angle.It is exactly the position that gus gene is expressed that plant is dyed blue position.Explore P by the expressive site and the expression intensity that detect gus gene under the different space-times _BnPABP3The spatial and temporal expression pattern.

This promoter-driven GUS gene efficiently expresses in the flower pesticide of Arabidopis thaliana, pollen granule, but does not express in the seed.Illustrating that this promotor has drives downstream gene and efficiently expresses in the flower pesticide of plant, pollen granule, and seed is not expressed.This promotor with tissue specific expression has using value in plant genetic engineering and transgenosis safety (eating).As containing the carrier that this promoters driven causes the gene of flower pesticide abortion by structure, the transformation receptor plant, the artificial male sterile material of creating, be applied in the production of cross-breeding, or the control transgenic plant are by the elegant genetically modified escape that causes of pollen, or some improves the gene of pollens nutrition composition by promoters driven, improves pollens nutrition etc.Simultaneously because P _BnPABP3The gene that drives is not expressed in seed, therefore can not occur the protein product of external source quiding gene in seed, has important use in transgenosis food safety field and is worth.

A kind of rape P _BnPABP3The description of promotor full length sequence SEQ ID NO:1 functional expression in plant tissue.Utilize genomic walking method clone to obtain 5 ' upstream sequence of swede type rape BnPABP3 gene, through core promoter element and Upstream cis acting promotor forecasting software http://www.fruitfly.org/seq_tools/promoter.html and PLACE (Higo et al., Plant cis-acting regulatory DNA elements (PLACE) database (J) .Nucleic Acids Research.1999,27:297～300) http://www.dna.affrc.go.jp/PLACE/ predicts.Obtain possible core promoter sequence and upstream promoter element (Fig. 3).The analyses and prediction result determines P _BnABP3Promoter sequence length.P _BnPABP3The native gene that drives is expressed in bud, does not express in other tissue.This illustrates P _BnPABP3The native gene that drives is a gene that efficiently expresses in bud, proves P _BnPABP3It is high efficient expression starter in the bud.

A kind of swede type rape P _BnPABP3The description of the application of promotor in flower pesticide and pollen granule.By the quantitative fluorescent PCR analysis, the native gene that the result shows this promoters driven spend, Ct value in the angle fruit, root, stem, leaf is respectively 25.54,32.08,34.05,33.03,37.76, and the Ct value of the Actin in above-mentioned tissue is respectively 18.69,18.24,17.71,17.13,17.02, shows that this promotor is a strong promoter of expressing in spending.Utilize genomic walking method clone to obtain rape P _BnPABP35 ' upstream sequence of the native gene that drives.Structure is by the plant expression vector pBI-P of the reporter gene GUS of this promoter regulation _BnPABP3(front is stated).Adopt agriculture bacillus mediated florescence infestation method arabidopsis thaliana transformation, T1 is for being added with preliminary screening transfer-gen plant on the MS of kantlex (front the is stated) substratum, after Arabidopis thaliana grows two true leaves, be transplanted to and continue plantation on the vermiculite, after inflorescence appears in plant, carry out PCR and detect, utilize the molecule means to identify positive strain.T2 is for selecting 10 transgenic lines to carry out GUS dyeing.GUS histochemical method dyeing shows, this promoter-driven GUS gene is expressed in the flower pesticide of Arabidopis thaliana and pollen granule.This shows that this promoter-driven GUS gene has certain spatial and temporal expression specificity, have the downstream gene of driving and in flower pesticide and pollen granule, express, do not express the function of (Fig. 6) in the seed fully.This promotor with tissue specific expression has using value in manual creation germ plasm resource, plant genetic engineering and transgenosis safety (eating), as utilizes this promotor to drive with pollen granule and grow relevant goal gene, at first makes up P _BnPABP3The expression vector excessively of driving purposes gene, the transformation receptor plant, then goal gene is at P _BnPABP3Under the driving of promotor, can improve the expression amount of goal gene in above-mentioned tissue, not express fully in the seed, can not cause food-safety problem.

Advantage of the present invention:

1, the promotor that the promotor cloning process that is provided is cloned into can obtain to have the rape promotor of tissue specific expression function by regulation and control and the group fractional analysis to gus gene.

2, be cloned into the P in rape source _BnPABP3From the security of rape edible oil with utilize the genetically modified crops quality, aspects such as manual creation germ plasm resource consider that this promotor has application potential.Use P _BnPABP3Replace the 35S promoter sequence on pBI121 (front the is stated) plasmid, form pBI-P _BnPABP3The recombinant plant expression vector, gus gene wherein is subjected to P _BnPABP3Regulation and control.Prove by transgenic experiments, the characteristic enlightenment applicant that the high strength of this promotor in flower pesticide and pollen granule drives the expression of gus gene and do not drive the expression of gus gene fully in seed can come replaced C aMV35S strong promoter to drive the gene relevant with pollen development with this promotor, make this gene overexpression in pollen, artificial sterile line, the recovery system of creating, enrich germ plasm resource, or the biological safety of raising transgenic plant, suppress the diffusion of foreign gene, prevent that gene from drifting about.

Description of drawings

Fig. 1 is a kind of P _BnPABP3The expression pattern analysis chart of the native gene that drives.

Fig. 2 is a kind of genomic walking amplification P _BnPABP3The fragment electrophorogram.

Swimming lane 1,2,3,4 is represented the pcr amplification result in four genomic dnas " storehouse " that form respectively after Dra I, EcoR V, Pvu II and Stu I enzyme are cut; Swimming lane M represents the nucleic acid Marker of DL2000.

Fig. 3 is a kind of P _BnPABP3The promoter sequence analysis chart.

Square frame and the underscore representative element relevant with anther-specific expression; Shade is represented primary element; Black matrix adds shade and represents ABRE motif; Runic adds square frame C, and runic ATG representative is transcribed and translation initiation site;

Fig. 4 is a kind of pBI-P of structure _BnPABP3The carrier synoptic diagram.

Fig. 5 is a kind of conversion carrier pBI-P _BnPABP3Part transfer-gen plant PCR identify figure

Swimming lane M represents the nucleic acid Marker of DL2000; Swimming lane 1 is represented pBI-P _BnPABP3The pcr amplification result of positive plasmid; The pcr amplification result of swimming lane 2,3,4,5,6 positive strains: the pcr amplification result of swimming lane 7 wild-type Arabidopis thalianas.

Fig. 6 is a kind of P _BnPABP3The histochemical stain result of driven GUS gene.

A:15 day seedling (colourless); B: inflorescence (the blue look of flower pesticide); C: not open bud (the blue look of flower pesticide); D: open bud (the blue look of flower pesticide); E angle fruit (colourless); F: flower pesticide (blue look); G: column cap (colourless); H: pollen granule (blue look); Bar=100 μ m.

Embodiment

According to following examples, can better understand the present invention, but described embodiment is in order better to explain the present invention rather than limitation of the present invention.

Embodiment 1:

Rape P _BnPABP3The expression pattern analysis of the native gene that drives:

The used rape of the present invention is swede type rape (Brassica napus L.).Be seeded in the land for growing field crops for the examination material, normal field management.

Get root, stem, leaf, bud, angle fruit from the identical fertile plant of grown in field condition, every kind of material is got three repetitions at least, and each repeats at least one strain, and the sampling back is positioned in the liquid nitrogen-80 ℃ of preservations rapidly with the masking foil parcel.Extract RNA (the method front is stated).Quantitative real time PCR Instrument is RT ^TM-Cycler (Boao Biological Co., Ltd), adopt rape Actin (accession number AF111812) as internal standard gene, the Actin gene primer be forward primer 5 '-CTGGAATTGCTGACCGTATGAG-3 ' and reverse primer 5 '-ATCTGTTGGAAAGTGCTGAGGG-3 '.Rape P _BnPABP3The native gene primer that drives is 5 '-GGGAAGATGATAGGAAGGAAA-3 ' and 5 '-CTGGTGCTCTAATCTGTGAAAA-3 '.

The quantitative fluorescent PCR reaction system is 20 μ L: contain SYBR Mix 10 μ L, and each 0.8 μ L of forward and reverse primer (10 μ mol/L), template 2 μ L, the sterilized water that DEPC handled complements to 20 μ L.Amplification condition is: 94 ℃, and 5min:94 ℃, 15s, 60 ℃, 20s, 72 ℃, 30s, 40 circulations; Each is circulated in 72 ℃ of renaturation ends and carries out fluoroscopic examination.Reaction is heated to 95 ℃ earlier after finishing, and reduces to 72 ℃ then, slowly is warming up to 95 ℃ again, writes down the variation of fluorescent signal, draws the melting curve of amplified production.Every group of experiment all finished three biology and repeated, and each biology repeats to do at least three technology and repeats.Detect P respectively _BnPABP3The expression of the native gene that drives in rape tissue (root, stem, leaf, flower, angle fruit).

Calculate the relative expression quantity of gene with comparing Ct method (Δ Δ Ct).Utilize software that instrument is with, at first optimize internal standard gene and goal gene amplification condition, measure the Ct value of Actin and goal gene respectively, choose that the most approaching three results (systematic error of Ct value is less than 0.3) average in nine measured value of experiment, by internal standard gene goal gene is proofreaied and correct then and obtained Δ Δ Ct, at last by 2 ^{-Δ Δ Ct}The relative expression quantity and systematic error (the Kenneth J Livak.Thomas D Schmittgen Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2 of estimation goal gene ^{-Δ Δ C}T Method METHODS 25,402-408 (2001)).When calculating relative expression quantity, be reference with the sample of bud, be about to its value and convert 1 to, other sample again with its relatively, obtain relative expression's value.

The result shows: P _BnPABP3The native gene that drives is expressed (Fig. 1) in bud, do not express in other tissue.This illustrates P _BnPABP3The native gene that drives is a gene that efficiently expresses in bud, proves P _BnPABP3It is a high efficient expression starter.

Embodiment 2:

A kind of swede type rape promotor P _BnPABP3The preparation method of promotor the steps include:

A, rape P _BnPABP3The promoter primer design:

Utilize the SDS cracking process to extract rape DNA (J. Sa nurse Brooker .D.W. Russell work, Huang Peitang etc. translate molecular cloning test guide (third edition) Science Press), according to the genomic walking test kit (available from Clontech company, product code name Cat.No.638904) schedule of operation, carry out genomic walking, the capable two-wheeled pcr amplification of step shift-in, the clone obtains rape P _BnPABP3(942bp).Step is moved the primer such as table 2.

Table 2 genomic walking clone P _BnPABP3The primer

B, swede type rape P _BnPABP3The promotor preparation is:

According to the genomic walking test kit (available from Clontech company, product code name Cat.No.638904) explanation, respectively with producing flat terminal restriction enzyme DraI, EcoRV, PvuII and StuI cuts about 2.5 μ g at 100 μ l system endoenzymes genomic dna, setting up four " storehouses " through restriction enzyme DNA that handle, that be connected with the specificity joint, is that template is carried out two-wheeled PCR reaction with it.Get 1 μ lDNA (1 μ g/ μ L) and cut, detect its purity with Dra I enzyme.System is as follows: DNA 5 μ l, Dra I (10 units/μ l) 1.6 μ l, 10 * buffer, 2 μ l, sterilized water polishing to 20 μ l.37 ℃, spend the night, detect enzyme with 1% (front is stated) agarose gel electrophoresis and cut effect.Cut DNA with DraI, EcoRV, PvuII and StuI enzyme respectively, reaction system is as follows: DNA (0.1 μ g/ μ l) 25 μ l, and EcoRV (10 units/μ l) 8 μ l, 10 * buffer, 10 μ l, sterilized water polishing to 100 μ l, 37 ℃ are spent the night.Cut the 3M NaOAc of adding 10 μ l in the liquid and the 95% (volume ratio of 50 μ l to enzyme, below identical) ethanol,-20 ℃ precipitate more than 3 hours down, 12000rpm is centrifugal 5 minutes then, 70% (volume ratio, below identical) washing with alcohol twice, centrifugal 5 minutes of 12000rpm, (20-25 ℃) dries under the room temperature, with 20 μ l sterilized waters dissolving air dried DNA.The reaction system that the specificity joint connects is as follows: 10 * T4 ligase buffer, 2.0 μ l, enzyme cut the DNA 8.0 μ l of processing, T4 ligase (1 unit/μ l) 1 μ l, and AP1 (25 μ M) 4.0 μ l, sterilized water is mended to 20 μ l, and 16 ℃ are spent the night.To connect liquid with 10 times of distilled water dilutions, be stored in-20 ℃.Carry out first round PCR reaction with genomic walking Auele Specific Primer GSP1 (table 2), system is as follows: 10 * buffer (MgCl ₂Free) 5 μ l, dNTPs mixture (10mM) 1.0 μ l, GSP1 (10 μ M) 2.5 μ l, AP1 (10 μ M) 2.5 μ l, Taq polymerase (5 units/μ l) 0.2 μ l connects liquid 0.1 μ l, and sterilized water is mended to 50 μ l.Response procedures is as follows: 94 ℃ of 1min; 98 ℃ of 10s, 72 ℃ of 2min, totally 7 circulations; 98 ℃ of 10s, 68 ℃ of 2min, totally 33 circulations; 72 ℃ of 10min., carry out second with genomic walking Auele Specific Primer GSP2 (table 2) and take turns the PCR reaction as second template of taking turns the PCR reaction with 50 times of distilled water dilution first round PCR reaction product, reaction system is as follows: 10 * buffer (no MgCl ₂) 5 μ l, dNTPs mixture (10mM) 1.0 μ l, GSP2 (10 μ M) 2.5 μ l, AP2 (10 μ M) 2.5 μ l, Taq polysaccharase (5 units/μ l) 0.2 μ l, template solution 1.0 μ l, sterilized water is mended to 50 μ l.Response procedures is with first round PCR reaction, pcr amplification result such as Fig. 2.Reclaim purifying second and take turns the PCR product, and connect, transformed into escherichia coli competence (front is stated), order-checking in order-checking T carrier (front is stated).Obtain P _BnPABP3Full length sequence, called after P _BnPABP3, a kind of isolating promotor, its series be the nucleotide sequence shown in the SEQ ID No.1 or with SEQ ID No.1 homologous nucleotide sequence in fact.

Rape P _BnPABP3The structure of recombinant expression vector and agrobacterium tumefaciens transform:

Be connected with P with Xba I/Hind III double digestion _BnPABP3PMD18-P _BnPABP3(front is stated) and pBI121 (front is stated) plasmid.Gel reclaims each promoter fragment and pBI121 (front the is stated) fragment that enzyme scales off, and connects, and transformed into escherichia coli (the method front is stated) is built into plant expression vector pBI-P _BnPABP3(front is stated) (Fig. 5).Use freeze-thaw method (front is stated) to change this carrier over to agrobacterium tumefaciens EHA105 (front is stated) at last, contain select positive colony on kantlex (50mg/L) and the two resistant panel of Rifampin (50mg/L) after, whether contain target fragment with PCR checking.

Embodiment 3:

PBI-P _BnPABP3Arabidopis thaliana transform and PCR detects:

According to above-mentioned document (Zhang X R.et al.Agrobacterium-mediated transformation of Arabidopsis thaliana using the floral dip method.Nature, 2006,1:1-6) middle method for transformation arabidopsis thaliana transformation.According to the peculiar kalamycin resistance of transfer-gen plant, to grow containing on the MS that concentration is the 50mg/L kantlex (front the is stated) substratum, the green seedling of acquisition is tentatively thought positive seedling.After treating that green seedling grows two true leaves, it is transplanted in the vermiculite, treat that inflorescence appears in plant after, get a slice true leaf and extract genomic dna (front is stated) with the SDS method, be PCR and identify.Primer sequence is, 5 '-GAATTGTGAGCGGATAAC-3 ' and 5 '-ACATAAGGGACTGACCAC-3 '; The PCR reaction system is as follows: genomic dna template 1 μ L (about 50ng), 10 * Taq enzyme reaction buffer solution 2ul, 25mMMgCL ₂1.2ul, 2mM dNTP 1.5ul, each 0.2ul of 10uM primer, 0.3 Taq of unit enzyme, add sterilized water to 20 μ l.Response procedures is: 94 ℃ of sex change 5min, and 94 ℃ of 45s, 55 ℃ of 45s, 72 ℃ of 2min32 circulations, 72 ℃ are extended 5min.Detect the PCR reaction product with 1% (front is stated) agarose gel electrophoresis, the result shows P _BnPABP3Expression vector pBI-P _BnPABP3Successfully changed Arabidopis thaliana (Fig. 5) over to.Obtain the positive seedling of 10 strains altogether.

Embodiment 4:

Swede type rape P _BnPABP3The functional analysis of promotor:

The present invention clones first and obtains P _BnPABP3Sequence, and it has been carried out functional analysis.From embodiment 3, Arabidopis thaliana transforms and PCR detects that screening obtains in the step positive seedling T1 generation, selfing results seed (being T2 generation).The different times tissue of getting T2 generation 10 strain systems carries out GUS dyeing.

T2 is as follows for getting dyeing course: sample is immersed in GUS dye liquor (X-gluc 0.5mg/mL, phosphoric acid buffer 50mmol/L, each 0.5mmol/L of the Tripotassium iron hexacyanide and yellow prussiate of potash, EDTA 10mmol/L, Triton-x-100 0.001%, methyl alcohol 20% (volume ratio) vacuum suction 5 minutes, 37 ℃ are spent the night.Decoloured with alcohol-acetate (volume ratio is 1: 1) in second day, and bleached until blade, use distilled water rinsing 3-5 time afterwards, Stereo microscope (OLYMPUS SZX16) is taken pictures.Get the whole plant of different time sections seedling stage; Reproductive stage, blade are got tender leaf and mature leaf; The inflorescence of flower that flower took away and the bud of not opening; The angle fruit of different times is really got at the angle; Seed removes back about the 10 days seed of blooming.It is exactly the position that gus gene is expressed that plant is dyed blue position.

Coloration result is found (table 3, Fig. 6): in the whole growth process of Arabidopis thaliana, flower pesticide and pollen granule are dyed blueness; In the fruit of angle, blueness does not appear in seed, does not occur blue in other tissue.This shows that this promoter-driven GUS gene is mainly expressed, and does not express in other tissue in flower pesticide and pollen granule.

Experimental result shows, rape P _BnPABP3Have following biological function: this promoter-driven GUS gene is expressed in the flower pesticide of Arabidopis thaliana and pollen granule, does not express in other tissue.P _BnPABP3Gus gene under the regulation and control has certain spatial and temporal expression characteristic, and this illustrates P _BnPABP3Have and drive the function that downstream reporter gene GUS expresses in recipient plant.Under the regulation and control of this promotor, gus gene can be mainly meticulous expression in the flower pesticide of transfer-gen plant and pollen granule, and in other tissue, do not express (table 3, Fig. 6) fully.

This promotor with tissue specific expression has using value in plant genetic engineering and transgenosis safety (eating).

Embodiment 5:

A kind of swede type rape P _BnPABP3The application of promotor in flower pesticide and pollen granule the steps include:

Utilize genomic walking method clone to obtain rape P _BnPABP35 ' upstream sequence of the native gene that drives.Structure is by the plant expression vector pBI-P of the reporter gene GUS of this promoter regulation _BnPABP3(front is stated).Adopt agriculture bacillus mediated florescence infestation method arabidopsis thaliana transformation, T1 is for being added with preliminary screening transfer-gen plant on the MS of kantlex (front the is stated) substratum, after Arabidopis thaliana grows two true leaves, be transplanted to and continue plantation on the vermiculite, after inflorescence appears in plant, carry out PCR and detect, utilize the molecule means to identify positive strain.T2 is for selecting 10 transgenic lines to carry out GUS dyeing.GUS histochemical method dyeing shows, this promoter-driven GUS gene is expressed in the flower pesticide of Arabidopis thaliana and pollen granule.This shows that this promoter-driven GUS gene has certain spatial and temporal expression specificity, have the downstream gene of driving and in flower pesticide and pollen granule, express, do not express the function of (Fig. 6) in other tissue fully.This promotor with tissue specific expression has using value in plant genetic engineering and transgenosis safety (eating), as utilizes this promoters driven pollen fertility or the goal gene relevant with oleaginousness, at first makes up P _BnPABP3The expression vector excessively of driving purposes gene, the transformation receptor plant, then goal gene is at P _BnPABP3Under the driving of promotor, in flower pesticide and pollen granule, express, can improve the expression amount of goal gene in above-mentioned tissue, do not express fully in the seed, can not cause food-safety problem.

Table 3 P _BnPABP3Transgenic arabidopsis T2 is for the GUS dyeing cartogram of strain system

Strain system number

Positive

Root

Stem

Blade

Flower pesticide

The angle pericarp

Pollen granule

Seed

Wild-type (CK)

NO

NO

NO

NO

NO

NO

NO

NO

P BnPABP3-1

NO

NO

NO

NO

YES

NO

YES

NO

P BnPABP3-2

NO

NO

NO

NO

YES

NO

YES

NO

P BnPABP3-3

NO

NO

NO

NO

YES

NO

YES

NO

P BnPABP3-4

NO

NO

NO

NO

YES

NO

YES

NO

P BnPABP3-5

NO

NO

NO

NO

YES

NO

YES

NO

P BnPABP3-6

NO

NO

NO

NO

YES

NO

YES

NO

P BnPABP3-7

NO

NO

NO

NO

YES

NO

YES

NO

P BnPABP3-8

NO

NO

NO

NO

YES

NO

YES

NO

P BnPABP3-9

NO

NO

NO

NO

YES

NO

YES

NO

P BnPABP3-10

NO

NO

NO

NO

YES

NO

YES

NO

SEQUENCE?LISTING

＜110〉Inst. of Oil Crops, Chinese Academy of Agriculture

＜120〉preparation method of swede type rape PBnPABP3 promotor and application thereof

＜130〉preparation method of swede type rape PBnPABP3 promotor and application thereof

<160> 1

<170> PatentIn?version?3.1

<210> 1

<211> 1440

<212> DNA

＜213〉swede type rape P _BnPA The preparation method of BP3 promotor and application thereof

<400> 1

gagagagaga?gagagagaga?gagagagaga?gagagaggtg?ttcacctagc?agtatatata 60

aaaagaatca?tattgaagat?gtctagttaa?acttttgaag?aacttcatac?tatagttaca 120

gtaatccatg?atctggtcaa?aataatctaa?aaatagttta?gtgttctatt?tgtggtaatg 180

tagataaata?tcttagccat?gaccaaatca?gtagttccca?gattcgcaaa?ctctactcct 240

taagatagat?gggtgtttgt?tctgtaccat?tattatacaa?gctagtcaaa?tgttatcaat 300

acatttgtta?gtaattagta?tgtatatatg?agggaatacc?acaaatataa?ttaaaaataa 360

aaatgatcat?cttgagtgta?ttaaatttta?ttcaacatgg?tcaagtaaat?ctggtcagac 420

gtcggtagat?cttcgtagaa?cggctaaagt?gatgcaatta?ggcataggtc?tacataaagc 480

acatagtatt?ttcggttgtc?gaatcttcta?tataatcttt?ctcgtatcat?aattgtaata 540

tcctaataaa?tcatcgttaa?aaaaaaaact?aaaaaattaa?gattttgtat?aaaactttaa 600

aatattaaat?catgtgactt?ccgtataaac?cattctatat?ataatatttt?ttttgagaaa 660

atatatatag?ttatttaact?tctaaaatca?gtataatata?gtattgatat?tgtttattat 720

tcataaatat?tttgatatta?tgtatgttaa?tatatttcta?aataacattc?taagagttac 780

gttcttatta?aaaaatgtta?tcaatatctt?agatcatttg?tattatttct?aaaatcttaa 840

attataacat?atacgaaaat?attatggtct?aatggtttat?aaaaagattt?ggttcgttac 900

acctttcagt?tttttgtgtt?atagaactat?atgaatcatc?tagttccaga?ctcactgaga 960

tatattattt?tatcctgatt?tttcttatgg?tgtataaaaa?agcactacta?atgtgaaaga 1020

gacatcatca?tcctgaattt?tgagactata?aaacacacac?aaacaagtaa?aaatacaaga 1080

gaagaaaaaa?aattgtaact?cttttcatat?taaaaataaa?taaaataagt?cattttctca 1140

tctataaata?ccttagacac?actcttcaca?tcgattcgat?tttcccctca?ccaatccctc 1200

tcgatcattg?gaggaaaaaa?ctaaaaggca?aaaaaaaatc?gacataagaa?taaaaacaat 1260

ttccctttaa?aataaggaaa?ttataaactt?cgaagaaaat?atacaaaaca?caatctctca 1320

cacttaaagc?ccctagagaa?tctaatcctc?ccattattct?ttttaggatc?ggtgattctc 1380

taaaaaggta?aacgcacgag?catggcggcc?gcggttgcga?cgggggttgc?accgtcgaca 1440

 

Claims (5)

1. isolating promotor P _BnPABP3 , its sequence is the nucleotide sequence shown in the SEQ ID No.1.

2. a kind of isolating promotor according to claim 1, it is characterized in that: described promotor contains recombinant vectors pBI- P _BnPABP3

3. the described a kind of swede type rape of claim 1 P _BnPABP3 The preparation method of promotor the steps include:

A, rape P _BnPABP3 The promoter primer design:

Utilize the SDS cracking process to extract rape DNA,, carry out genomic walking according to genomic walking test kit schedule of operation, the capable two-wheeled pcr amplification of step shift-in, the clone obtains rape P _BnPABP3 , the step moves the primer and is:

AP1：5'–GTAATACGACTCACTATAGGGC–3'；GSP1：5'–TTGATCAGCCGCAACCACTGGAGATTG–3'；AP2：5'–ACTATAGGGCACGCGTGGT–3'；GSP2：5'–TGATCAATCATTGTCGACGGTGCAACCC–3'；

B, swede type rape promotor P _BnPABP3 Preparation is:

According to the explanation of genomic walking test kit, get 5 μ l DNA and use DraThe I enzyme is cut, and detects its purity, and system is as follows: DNA 5 μ l, DraI 1.6 μ l, 10 * buffer, 2 μ l, sterilized water polishing to 20 μ l, 37 ℃, spend the night, detect enzyme with 1% mass volume ratio agarose gel electrophoresis and cut effect, respectively with producing flat terminal restriction enzyme DraI, EcoRV, PvuII and StuI cuts the genomic dna of 2.5 μ g at 100 μ l system endoenzymes, the reaction system of four kinds of restriction enzymes is as follows: DNA 2.5 μ g, restriction enzyme 8 μ l, 10 * buffer, 10 μ l, sterilized water polishing to 100 μ l, 37 ℃ are spent the night, enzyme cuts the back purifying, purification step is as follows: cut the 3M NaOAc of adding 10 μ l in the liquid and the 95% volume ratio ethanol of 50 μ l to enzyme,-20 ℃ precipitate 3 hours down, 12000rpm is centrifugal 15 minutes then, twice of 70% volume ratio washing with alcohol, centrifugal 5 minutes of 12000 rpm, dry under the room temperature, dissolve with 20 μ l sterilized waters, after finishing, purifying adds the specificity joint, reaction system is as follows: 10 * T4 ligase buffer, 2.0 μ l, above-mentioned enzyme is cut the DNA 8.0 μ l of processing, T4 ligase 1 μ l, specificity joint 14.0 μ l, sterilized water is mended to 20 μ l, and 16 ℃ are spent the night, and will connect liquid and dilute 10 times with distilled water, be stored in-20 ℃, having set up four and handled and be connected with the dna library of specificity joint through restriction enzyme, is that template is carried out two-wheeled PCR reaction with it, and first round PCR reaction is a primer with GSP1 and AP1, system is as follows: 10 * buffer, 5 μ l, dNTPs mixture 1.0 μ l, GSP1 2.5 μ l, AP1 2.5 μ l, Taq enzyme 0.2 μ l, the dna library 0.1 μ l of dilution, sterilized water is mended to 50 μ l, and response procedures is as follows: 94 ℃ of 1min; 98 ℃ of 10s, 72 ℃ of 2min, totally 7 circulations; 98 ℃ of 10s, 68 ℃ of 2min, totally 33 circulations; 72 ℃ of 10min, second take turns PCR with 50 times of diluents of first round PCR reaction product as template, be that primer increases with GSP2 and AP2, reaction system is as follows: 10 * buffer, 5 μ l, dNTPs mixture 1.0 μ l, GSP2 2.5 μ l, AP2 2.5 μ l, Taq enzyme 0.2 μ l, dilution template solution 1.0 μ l, sterilized water is mended to 50 μ l, response procedures is with first round PCR, reclaim purifying second after finishing and take turns the PCR product, and be connected, obtain through order-checking with the T carrier P _BnPABP3 Full length sequence.

4. claims 1 described a kind of isolating promotor P _BnPABP3 Application in flower pesticide.

5. claims 1 described a kind of isolating promotor P _BnPABP3 Application in pollen granule.

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