CN103923923B - Derive from heavy metal evoked promoter and the application thereof of Arabidopis thaliana - Google Patents
Derive from heavy metal evoked promoter and the application thereof of Arabidopis thaliana Download PDFInfo
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Abstract
The invention discloses the heavy metal evoked promoter and application thereof that derive from Arabidopis thaliana.Does is this promotor that plant is subject to heavy metal evoked promoter, and name is called AtMT1a promotor, is following DNA molecular a), b) or c): a) nucleotide sequence is SEQ? ID? the DNA molecular of No.1; B) nucleotide sequence and a) limited has more than 75% or 75% consistence, and has the DNA molecular of promoter function; C) under high high stringency conditions with nucleotide sequence hybridization a) or b) limited, and there is the DNA molecular of promoter function.AtMT1a promotor of the present invention is significant to the resistance being improved transgenic plant heavy metal by the high expression level of goal gene under heavy metal stress, and AtMT1a promotor of the present invention also can be used for cultivating heavy metal pollution of soil early warning transgenic plant.
Description
Technical field
The present invention relates to the heavy metal evoked promoter and application thereof that derive from Arabidopis thaliana.
Background technology
In plant transgenic technology, high expression goal gene, be unable to do without efficient promotor.Promotor (Promoter) to refer on DNA sequence dna by RNA polymerase identification and forms the region of transcription initiation complex.Promotor is usually located at upstream region of gene, is the sequence of controlling gene transcription initiation, and decides the expression intensity of a certain gene.The cultivation of exploitation strong promoter to genetically modified crops is significant.In plant genetic engineering, conventional promotor can be divided three classes: constitutive promoter, inducible promoter and tissue-specific promoter.Constitutive promoter in a organized way in all promotor gene express, have persistence, do not show Space-time speciality, RNA and protein expression amount are also relative constancy.This type of representative promotor has tobacco mosaic virus (TMV) CaMV35S promotor, Maize Ubiquitin gene Ubiquitin promotor and rice actin gene Actin promotor etc.The feature of inducible promoter is, under normal circumstances can not the expression of promotor gene, but after the stimulation by some physics, chemistry, bio signal, the promotor of this type can improve the transcriptional level of gene significantly, as Arabidopis thaliana low temperature induction promotor rd29A.The feature of tissue-specific promoter is, the expression of its Downstream regulatory gene often only occurs in some specific Organ and tissue, and often shows the characteristic of Growth adjustment, as specific expression gene promotor TA29 in tobacco pollen tapetal cell.
But there are problems in actual applications in constitutive promoter.One, constitutive promoter can derive from virus, microorganism or animal (as CaMV35S promotor derives from virus), and consider from Biosafety angle, it have impact on the popularization of genetically modified crops to a certain extent.They are two years old, recent research shows that constitutive promoter is due to overexpression goal gene in plant materials, consume more material and energy in cell, while enhancing plant target resistance, but have a strong impact on plant normal growth and grow (as transgenic wheat, paddy rice, Arabidopis thaliana show the symptoms such as plant dwarfing, delayed growth).They are three years old, due to the specificity that constitutive promoter does not have Organ and tissue to express, the toxic products (as Bt toxalbumin) of genetic expression can be caused to generate in crop kernel (or edible position), and this is another Biosafety hidden danger of constitutive promoter.Along with the development of transgenic technology, urgently develop how efficient inducible promoter or tissue-specific promoter.Therefore, directly from the new promotor of plant cloning high expression, there is important using value.
Summary of the invention
Technical problem to be solved by this invention is to provide plant by heavy metal evoked promoter.
Plant provided by the present invention is by heavy metal evoked promoter, and name is called AtMT1a promotor, derives from Ler Arabidopsis thaliana ecotype, is following DNA molecular a), b) or c):
A) nucleotide sequence is the DNA molecular of SEQIDNo.1;
B) nucleotide sequence and a) limited has more than 75% or 75% consistence, and has the DNA molecular of promoter function;
C) under high high stringency conditions with nucleotide sequence hybridization a) or b) limited, and there is the DNA molecular of promoter function.
Wherein, SEQIDNo.1 is made up of 1140 Nucleotide.
More than above-mentioned 75% or 75% consistence, can be the consistence of 80%, 85%, 90%, more than 95%.
Described high high stringency conditions refers to, is placed in by Hybond membrane in prehybridization solution (0.25mol/L sodium phosphate buffer, pH7.2,7%SDS), 65 DEG C of prehybridization 30min; Abandon prehybridization solution, add hybridization solution (0.25mol/L sodium phosphate buffer, pH7.2,7%SDS, isotope-labeled nucleotide fragments), 65 DEG C of hybridization 12hr; Abandon hybridization solution, add film washing liquid I (20mmol/L sodium phosphate buffer, pH7.2,5%SDS), wash film 2 times, each 30min for 65 DEG C; Add film washing liquid II (20mmol/L sodium phosphate buffer, pH7.2,1%SDS), wash film 30min for 65 DEG C.
Those of ordinary skill in the art can adopt known method easily, the method for such as orthogenesis and point mutation, suddenly change to promotor nucleotide sequence of the present invention.Those are through manually modified, there is the Nucleotide being separated promotor the nucleotide sequence 70% or higher homology obtained with the present invention, as long as maintain the promoter activity of expressing target gene, be all be derived from nucleotide sequence of the present invention and be equal to sequence of the present invention.
Term used herein " homology " refers to the sequence similarity with native sequence nucleic acid." homology " comprises and to have preferably 75% or higher with promotor nucleotide sequence of the present invention, and more preferably 85% or higher, even more preferably 90% or higher, and the nucleotide sequence of most preferably 95% or higher identity.Homology can with the naked eye or computer software evaluate.Use computer software, the homology between two or more sequence can represent with per-cent (%), and it can be used for evaluating the homology between correlated series.
Expression cassette containing AtMT1a promotor, recombinant vectors, recombinant microorganism or transgenic cell line also belong to protection scope of the present invention.
The described expression cassette containing AtMT1a promotor, refers to the DNA that can express goal gene in host cell, and this DNA not only comprises the AtMT1a promotor starting described goal gene and transcribe, and also can comprise the terminator stopping described goal gene and transcribe.Further, described expression cassette also can comprise enhancer sequence.Described transcription terminator includes but not limited to: Agrobacterium nopaline syntase terminator (NOS terminator), cauliflower mosaic virus CaMV35S terminator, tml terminator, pea rbcSE9 terminator and nopaline and octopine synthase terminator (see, such as: the people (I such as Odell
985) Nature313:810; The people such as Rosenberg (1987) Gene, 56:125; The people such as Guerineau (1991) Mol.Gen.Genet, 262:141; Proudfoot (1991) Cell, 64:671; The people GenesDev. such as Sanfacon, 5:141; The people such as Mogen (1990) PlantCell, 2:1261; The people such as Munroe (1990) Gene, 91:151; The people such as Ballad (1989) NucleicAcidsRes.17:7891; The people such as Joshi (1987) NucleicAcidRes., 15:9627).
The promotor AtMT1a promotor shown in 1-1140 position of the described concrete available SEQIDNo.1 of recombinant vectors containing AtMT1a promotor is replaced fragment between the BamH I of pCAMBIA1381 and SpeI and is obtained the gus gene recombinant expression vector pCAMBIA1381-AtMT1a – GUS of AtMT1a promoters driven.Described recombinant microorganism specifically can be bacterium, yeast, algae and fungi.Wherein, bacterium can from Escherichia (Escherichia), Erwinia (Erwinia), agrobacterium tumefaciens belongs to (Agrobacterium), Flavobacterium (Flavobacterium), Alcaligenes (Alcaligenes), Rhodopseudomonas (Pseudomonas), Bacillus (Bacillus) etc.Described transgenic cell line does not comprise the reproductive material of animal and plant.
In the present invention, the plant tissue of conversion by using including but not limited to Ti-plasmids, Ri plasmid, plant viral vector, directly delivered DNA, microinjection, conductance, conventional biology methods transformed plant cells or the tissue such as agriculture bacillus mediated, and is cultivated into plant by the plant expression vector carrying AtMT1a promotor.
The primer pair of amplification AtMT1a promotor total length or its arbitrary fragment also belongs to protection scope of the present invention.
Experiment proves, AtMT1a promotor can start destination gene expression under heavy metal induction, and it is different at the different growing stage expressive site of plant, at the Seedling Stage of Arabidopis thaliana, after heavy metal induction, in predominant expression in root, express more weak in cotyledon, vegetative period afterwards, in predominant expression in the vascular bundle of cotyledon and lotus throne leaf.
AtMT1a promotor starts the application that goal gene expresses in plant and also belongs to protection scope of the present invention under heavy metal stress.In this application, described startup goal gene express in plant specifically can be start goal gene in the cotyledon of Arabidopis thaliana and the vascular bundle of lotus throne leaf, express (specifically expressing).
AtMT1a promotor can be used for cultivating transgenic plant, and these transgenic plant can increase the expression amount of goal gene under heavy metal induction.
Above, described heavy metal can be divalent heavy metal ions.Described divalent heavy metal ions can be Cd
2+, Cu
2+and/or Zn
2+.
In above-mentioned application, described plant can be monocotyledons or dicotyledons, and described dicotyledons can be cress, as Arabidopis thaliana.
Described transgenic plant are interpreted as the first-generation transgenic plant not only comprising and obtained by AtMT1a promotor conversion object plant, also comprise its filial generation.For transgenic plant, this gene can be bred in these species, also with traditional breeding method, the transfer of this AtMT1a promotor can be entered other kind of same species, particularly including in commercial variety.Described transgenic plant comprise seed, callus, whole plant and cell.
AtMT1a promotor of the present invention is attached most importance to metal inducible promoter.Utilize AtMT1a promotor that gene can be made to express under heavy metal inductive condition, thus avoid negative interaction that constitutive promoter overexpression brings-produce a large amount of heterologous proteins and toxic substance.AtMT1a promotor of the present invention is significant to the resistance being improved transgenic plant heavy metal by the high expression of startup target resistant gene under heavy metal stress, and AtMT1a promotor of the present invention also can be used for cultivating heavy metal pollution of soil early warning transgenic plant.
Accompanying drawing explanation
Fig. 1 is the pcr amplification product electrophoretogram of AtMT1a promotor.
In figure, M, MarkerIII; The pcr amplification product of 1, AtMT1a promotor.
Fig. 2 is the structure schematic flow sheet of pCAMBIA1381-AtMT1a – GUS.
Fig. 3 is the genetic conversion system of Arabidopis thaliana.
In Fig. 3, A, the plantation of Arabidopis thaliana; B, the Arabidopis thaliana of blooming; C, the Arabidopis thaliana that Agrobacterium was infected.
Fig. 4 is for turning pCAMBIA1381-AtMT1a – GUST
3gUS tissue specificity for Arabidopis thaliana is analyzed.
In Fig. 4, a-j be respectively growth 1 day, 3 days, 5 days, 10 days, 10 days, 15 days, 15 days, 20 days, 20 days, 20 days turn pCAMBIA1381-AtMT1a – GUST
3for Arabidopis thaliana, k is for contrasting-turning pCAMBIA1381T
3for Arabidopis thaliana.
Fig. 5 is the structure schema of pBI-AtMT1a-RFP.
Fig. 6 is for turning pBI-AtMT1a-RFPT
1for the growth photo of Arabidopsis thaliana Seedlings in the screening culture medium containing kantlex.
Fig. 7 be the kantlex positive turn pBI-AtMT1a-RFPT
1for the PCR detected result of Arabidopsis plant.
In Fig. 7, CK is pBI-AtMT1a-RFP (positive control), 1-20 be the 20 strain kantlex positives turn pBI-AtMT1a-RFPT
1strain for Arabidopis thaliana is numbered.
Fig. 8 is for turning pBI-AtMT1a-RFPT
2northern for Arabidopis thaliana detects.
Fig. 9 is that under different cadmium concentration, line-1 strain turns pBI-AtMT1a-RFPT
3for Arabidopsis leaf laser confocal microscope photo.In Fig. 9, a, b, c are respectively the Arabidopsis leaf of 10 μm of ol/LCd treatment group, 20 μm of ol/LCd treatment group and 100 μm of ol/LCd treatment group, and scalebars is 30 μm; D, e are respectively the Arabidopsis leaf of 10 μm of ol/LCd treatment group and 20 μm of ol/LCd treatment group, and scalebars is 5 μm; F is the Arabidopsis leaf of 0 μm of ol/LCd treatment group.
Figure 10 is that the line-1 strain of 0 μm of ol/LCd treatment group turns pBI-AtMT1a-RFPT
3for Arabidopis thaliana root laser confocal microscope photo.Scalebars is 50 μm.
Figure 11 is that the line-1 strain of 10 μm of ol/LCd treatment group turns pBI-AtMT1a-RFPT
3for Arabidopis thaliana root laser confocal microscope photo.Scalebars is 50 μm.
Figure 12 is that the line-4 strain of 10 μm of ol/LCd treatment group turns pBI-AtMT1a-RFPT
3for Arabidopis thaliana root laser confocal microscope photo.Scalebars is 50 μm.
Embodiment
Following examples further illustrate of the present invention, instead of limitation of the present invention.Without departing from the spirit and substance of the case in the present invention, amendment method of the present invention, step or condition done or replace and all belong to scope of the present invention.
If do not specialize, the conventional means that technique means used in embodiment is well known to those skilled in the art.
Molecular biology reagents conventional in following embodiment is TAKARA Products.
Plant expression vector pBI-121 (i.e. the pBI121 of Clontech company) in following embodiment (Sun Jingwen etc. the Cloning and Expression vector construction of three-coloured amaranth AmPCS gene. North China agronomy reports .2012.27 (2): 44-49), the public can obtain from Chinese Academy of Agricultural Sciences's agricultural resource and agricultural regionalization institute, this biomaterial related experiment of the present invention of only attaching most importance to again is used, not can be used as other purposes and uses.
Agrobacterium tumefaciens lba4404 (Shanghai Dongguo Biology Co., Ltd., production code member: MCC027-1) in following embodiment.
Ler Arabidopsis thaliana ecotype (Arabidopsisthaliana.Landsbergerecta) in following embodiment (effect of red .ABI1 and GPA1 of Li Yan in Arabidopis thaliana grows. Agriculture of Anhui science .2006,34 (18): 4507-4512) public can obtain from Chinese Academy of Agricultural Sciences's agricultural resource and agricultural regionalization institute, this biomaterial related experiment of the present invention of only attaching most importance to again is used, not can be used as other purposes and uses.
PCAMBIA1381 (the great Bioisystech Co., Ltd in Shanghai, production code member: MGT-M1702-C020) in following embodiment.
The solvent of the MS substratum in following embodiment is that water, solute are as shown in table 1.1/2MS substratum is all reduced by half at the macroelement of MS substratum, trace element and sucrose concentration, the minimum medium that other component is constant.1/2MS liquid nutrient medium is removed by the agar in 1/2MS substratum, other component and the constant substratum obtained of concentration.MS substratum in following embodiment, 1/2MS substratum, 1/2MS liquid nutrient medium, 1/2MS+10 μm ol/LCd
2+substratum, 1/2MS+20 μm ol/LCd
2+substratum and 1/2MS+100 μm of ol/LCd
2+the pH of substratum is 5.8.
The solute of table 1.MS substratum
The clone of embodiment 1, heavy metal inducible promoter AtMT1a promotor and functional verification thereof
1, the clone of AtMT1a promotor
With the genomic dna of Ler Arabidopsis thaliana ecotype blade for template, with P1:5 '-AT
gGATCCcATAGTTACGTAATCTTAAC-3 ' and P2:5 '-GC
aCTAGTcCGCAAGTTTTAGTTACGTA-3 ' carries out pcr amplification as primer, electrophoresis detection pcr amplification product, and result shows that this pcr amplification product size is about 1200bp (Fig. 1).Check order after this pcr amplification product is connected with pMD19-T cloning vector (TAKARA company).Sequencing result is shown the recombinant vectors called after pMD19-AtMT1a containing the DNA molecular shown in the 1-1140 position of SEQIDNo.1.Wherein, SEQIDNo.1 is made up of 1140 Nucleotide, is the nucleotide sequence of AtMT1a promotor.
2, the functional verification of AtMT1a promotor
2.1 containing the structure of AtMT1a promotor gus gene recombinant expression vector pCAMBIA1381-AtMT1a – GUS
With BamHI and SpeI two restriction enzymes cleaving plant expression vector pCAMBIA1381 and pMD19-AtMT1a simultaneously, reclaim AtMT1a promoter fragment and carrier large fragment T
4dNA ligase connects, and AtMT1a promotor is connected into the restriction enzyme site of pCAMBIA1381 carrier, obtains the recombinant expression vector pCAMBIA1381-AtMT1a – GUS transcribed by AtMT1a promotor startup gus gene.Confirm through order-checking, pCAMBIA1381-AtMT1a – GUS replaces fragment between BamHI and the SpeI site of pCAMBIA1381 for the AtMT1a promotor shown in the 1-1140 position with SEQIDNo.1, keeps the constant gus gene recombinant expression vector obtained of other sequence of pCAMBIA1381.PCAMBIA1381-AtMT1a – GUS carries damp enzyme element resistance, and it builds schematic flow sheet as shown in Figure 2.
2.2pCAMBIA1381-AtMT1a – GUS arabidopsis thaliana transformation
Getting 1 μ g recombinant plasmid pCAMBIA1381-AtMT1a – GUS is added in agrobacterium tumefaciens lba4404 competent cell, and ice bath 30 minutes, freezes in liquid nitrogen 8 minutes (5-8 minute), 37 DEG C of heat shocks 5 minutes; Add 1mlYEP (containing 50mg/Lrif, 28 DEG C, 200rpm shaking culture about 4 hours, 5000rpm, 2 minutes; Abandon supernatant 900 μ l, remaining bacterium liquid suction nozzle suspends, and moves on on YEP flat board (containing 50mg/Lrif, 100mg/LKm) and is coated with bacterium.28 DEG C, cultivate 2-3 days, select positive clone identification, obtain containing the recombinational agrobacterium of pCAMBIA1381-AtMT1a – GUS expression vector, called after LBA4404/pCAMBIA1381-AtMT1a – GUS, infect bacterium as genetic transformation Arabidopis thaliana.
Classical colored method (Clough and Bent, 1998) of being stained with is adopted to carry out genetic transformation to Ler Arabidopsis thaliana ecotype.In certain volume LB (50 μ g/ μ l kantlex, 50 μ g/ μ l gentamicins) nutrient solution, add LBA4404/pCAMBIA1381-AtMT1a – GUS bacterium liquid (100ml/6 strain) according to transformed plant quantity, 28 DEG C are shaken bacterium 24hr to OD600 and are about 0.5.Centrifugal, collection LBA4404/pCAMBIA1381-AtMT1a – GUS, and Eddy diffusion is about 0.8 to OD600 in MS (3% sucrose).Before conversion, in LBA4404/pCAMBIA1381-AtMT1a – GUS bacterium liquid, add the SilwetL-77 of 0.005%, and remove flower open on plant and fruit pod.Whole plant is immersed bacterium liquid 15min, and place 16 ~ 24 hours in dark, moist environment, then continue normal cultivation, and again transformed after one week.Stop after seed maturity watering, within about one month, gather in the crops seed later.Collect pCAMBIA1381-AtMT1a – GUS and transform (T in the present age
0generation) T that ties of Arabidopsis plant
1the seed (Fig. 3) in generation, obtains turning pCAMBIA1381-AtMT1a – GUST
1for Arabidopis thaliana seed.
Get and turn pCAMBIA1381-AtMT1a – GUST
1be layered on screening culture medium (1/2MS+50 μ g/ml Totomycin) upper cultivation about 1 week for Arabidopis thaliana seed, select root can the plantlet of transplant of normal growth in flowerpot, cultivate in 22 DEG C of greenhouses, remove terminal bud to promote that lateral bud grows.Get blade after cultivating for some time and extract genomic dna in a small amount, identify positive plant by PCR method.Collect the seed of positive seedling (pcr amplification product of about 1200bp can be obtained with primer pair P1 and P2), and number.Continue to turn pCAMBIA1381-AtMT1a – GUST to what gather in the crops
2screen for Arabidopis thaliana seed, obtain and turn pCAMBIA1381-AtMT1a – GUST
3for Arabidopis thaliana seed, identify for next step promoter function.According to above-mentioned same procedure, transform Ler Arabidopsis thaliana ecotype with pCAMBIA1381, obtain turning pCAMBIA1381T
3for Arabidopis thaliana seed, as empty vector control.
The Histochemical localization of 2.3pCAMBIA1381-AtMT1a – GUS arabidopsis thaliana transformation
Experiment in triplicate, repeats to turn pCAMBIA1381-AtMT1a – GUST at every turn
3for Arabidopis thaliana seed, turn pCAMBIA1381T
3plant respectively in screening culture medium (1/2MS+50 μ g/ml Totomycin) for Arabidopis thaliana seed and these three strains of Ler Arabidopsis thaliana ecotype seed, each strain arranges following 10 kinds of process respectively: cultivate respectively 1 day (in Fig. 4 a), 3 days (in Fig. 4 b), 5 days (in Fig. 4 c), 10 days (in Fig. 4 d), 10 days (in Fig. 4 e), 15 days (in Fig. 4 f), 15 days (in Fig. 4 g), 20 days (in Fig. 4 h), within 20 days, (in Fig. 4, i) He 20 days (in Fig. 4 j).The plant each strain often being planted process is divided into two groups of-Cd
2+induction group and water treatment group, often organize 5 strains.By Cd
2+the plant of induction group and water treatment group is taken out respectively, by Cd
2+the root system of induction group plant is all placed in 100 μMs of CdCl
2within in the aqueous solution 24 hours, carry out Cd
2+induction, is all placed in water 24 hours as not through Cd using the root system of water treatment group plant
2+the contrast of induction, then takes out Cd
2+the plant of induction group and water treatment group proceeds to GUS staining fluid respectively, makes the volume ratio of material and GUS staining fluid be 1:5.Put into 37 DEG C of thermostat containers to be incubated overnight.Infiltrate after in material until GUS, material proceeds in transparent liquid transparent, to slough chlorophyll, is positioned over 3-5 hour under room temperature, until green is removed completely.Vegetable material after transparent processing is at dissection Microscopic observation, and the position having GUS to express manifests stable, to be insoluble to transparent liquid blueness, and anatomical lens connects digital photo camera, is used for gathering photograph.With the various organs of different development stage plant for material, carrying out GUS histochemical stain, to analyze AtMT1a promotor tissue expression specificity as follows: result shows through Cd
2+induction and not through Cd
2+the all of each vegetative period of induction turn pCAMBIA1381 empty carrier T
3for all not detecting in all organs of Arabidopis thaliana and Ler Arabidopsis thaliana ecotype plant that gus gene is expressed (in Fig. 4 k).Through Cd
2+the all of induction turn pCAMBIA1381-AtMT1a – GUST
3be predominant expression for Arabidopis thaliana sprouting the underground part of 1-5 days size seedling, and express more weak in cotyledon, gus gene expresses (in Fig. 4 a-c) hardly at tip of a root position; But, along with turning pCAMBIA1381-AtMT1a – GUST
3for the further growth of Arabidopsis thaliana Seedlings, grow 10-20 days turn pCAMBIA1381-AtMT1a – GUST
3for in Arabidopsis plant, gus gene in the vascular bundle of cotyledon and lotus throne leaf in predominant expression (e, f in Fig. 4, h, i).Not through Cd
2+the all of growth 10 days of induction turn pCAMBIA1381-AtMT1a – GUST
3for the faint expression of gus gene (g in Fig. 4, j), but blueness is obviously shallower than through Cd being detected in the cotyledon of Arabidopsis plant and the vascular bundle of lotus throne leaf
2+the growth 10 days of induction turn pCAMBIA1381-AtMT1a – GUST
3for vascular bundle (e, f in Fig. 4, the h, i) of the cotyledon of Arabidopis thaliana and lotus throne leaf.
Wherein, GUS staining fluid preparation: (1) 100mlA liquid: take 19.907 grams of Na
2hPO
412H
2after O dissolves with sterile distilled water, constant volume is to 100ml; (2) 100mlB liquid: take 7.80 grams of NaH
2pO
42H
2after O dissolves with sterile distilled water, constant volume is to 100ml; (3) 10ml phosphoric acid buffer configuration: by 5.77mlA liquid and 4.23mlB liquid mixing (PH=7.0); (4) 100ml5mMK
4(Fe (CN)
6): claim 0.211 gram of K
4(Fe (CN)
6) 3H
2after O dissolves with sterile distilled water, constant volume is to 100ml; (5) 100ml5mMK
3(Fe (CN)
6): take 0.165 gram of K
3(Fe (CN)
6) dissolve rear constant volume to 100ml with sterile distilled water; (6) 10mg/mlX-Glue mother liquor configuration: take 10mgX-Glue, use 1ml dmso solution ,-20 DEG C of preservations; (7) configuration of GUS staining fluid: 4.0ml phosphoric acid buffer, 10 μ lTriton-100,20 μ lNa
2eDTA, 1.0ml5mMK
4(Fe (CN)
6), 1.0ml5mMK
3(Fe (CN)
6), 1.0mlX-Glue mother liquor, 3.0mlH
2o.
Transparent liquid forms: the acetic acid of the ethanol+10% of 90%.
The GUS activation analysis of 2.4pCAMBIA1381-AtMT1a – GUS arabidopsis thaliana transformation
Experiment in triplicate, repeats to turn pCAMBIA1381-AtMT1a – GUST at every turn
3for Arabidopis thaliana seed on 1/2MS substratum, get the growth seedling of 10 days and be divided into five groups: CK treatment group, H
2o treatment group, Cd treatment group, Cu treatment group and Zn treatment group, each treatment group 5 strain seedling.The seedling of CK treatment group places 24 hours as Quality Control, H in 1/2MS liquid nutrient medium
2the seedlings root of O treatment group is placed in sterile distilled water 24 hours as not through the contrast of heavy metal induction, and the seedlings root of Cd treatment group is placed in 100 μMs of CdCl
2within in solution 24 hours, carry out Cd
2+induction, the seedlings root of Cu treatment group is placed in 150 μMs of CuSO
4within in solution 24 hours, carry out Cu
2+induction, the seedlings root of Zn treatment group is placed in 2mMZnSO
4within in solution 24 hours, carry out Zn
2+induction.Except root system being placed in different liqs China and foreign countries in above-mentioned process, other envrionment conditions is all identical.The seedling leaves of above-mentioned respective handling of learning from else's experience carries out analysis GUS activity.Concrete grammar is as follows:
A, GUS extract
(1) 100mg blade is put in liquid nitrogen and is pulverized;
(2) Extraction buffer (50mM buffer solution of sodium phosphate (pH7.0), 10mM beta-mercaptoethanol, the 10mMNa of 5 times of volumes is added
2eDTA (pH8.0), 0.1%SDS, 0.1%TritonX-100), make homogenate;
(3) 10000r/min4 DEG C of centrifugal 10min, collects supernatant liquor, obtains blade GUS extracting solution.
B, GUS extracting solution determining the protein quantity
(1) production standard curve: preparation 0.2mg/mlBSA mother liquor: take 20mgBSA, add 0.5ml Extraction buffer, use H
2o constant volume 100ml.BSA gradient liquid is made by table 2:
Table 2
| BSA mother liquor (ml) | H 2O(ml) | BSA concentration (μ g/ml) |
| 0.0 | 5.0 | 0 |
| 0.25 | 4.75 | 10 |
| 0.5 | 4.5 | 20 |
| 1.0 | 4.0 | 40 |
| 1.5 | 3.5 | 60 |
| 2.0 | 3.0 | 80 |
| 2.5 | 2.5 | 100 |
(2) extracting solution determining the protein quantity: get blade GUS extracting solution 20 μ l, add H
2o to 4ml, adds 1ml Coomassie Brillant Blue solution, and mixing, ambient temperatare puts 2min.Measure 595nm absorbance value, according to typical curve calculation sample protein content.
C, GUS enzyme reaction
(1) get the GUS extracting solution 20 μ l of blade, add H
2o to 4ml, then add 1ml Coomassie Brillant Blue solution, fully mix, be placed in 37 DEG C of preheatings;
(2) get 5 Eppendorf centrifuge tubes, respectively add 900 μ l reaction terminating liquid (0.2MNa
2cO
3), numbering, obtains No. 1-5 pipe;
(3) reaction buffer that 1 Eppendorf centrifuge tube adds 500 μ l preheatings is got, add 100 μ l Extraction buffers again, mixing, takes out 100 μ l immediately and joins in No. 1 pipe, this is the sample (as blank during fluorometric assay) during reaction 0, and starts strict timing;
(4) reaction tubes is put into 37 DEG C of water-baths and carry out enzyme reaction, respectively at 20,40,60,80min time respectively get 100 μ l reaction solutions, join in 2-5 pipe successively, mixing, be respectively enzyme reaction 20,40,60,80min time sample, for fluorometric assay;
(5) at exciting light 365nm, the fluorescence intensity of each sample under utilizing emitted light 455nm, slit 10nm condition, is surveyed.
The amount producing 4-MU with per minute every milligram protein hydrolase 34-MUG represents that GUS is active.Result is as shown in table 3, CK treatment group, H
2in these five treatment group of O treatment group, Cd treatment group, Cu treatment group and Zn treatment group, the activity of Zn treatment group is the highest, is H
23.41 times of O treatment group, being secondly Cd treatment group and Cu treatment group, is H respectively
23.36 times of O treatment group and 2.82 times; CK treatment group and H
2o treatment group is quite active.Illustrate that AtMT1a promotor is through Cd
2+, Cu
2+and/or Zn
2+induction can significantly improve the expression amount of goal gene, thus prove that AtMT1a promotor is heavy metal inducible promoter.
The GUS of each treatment group plant of table 3. is active
| Treatment group | GUS activity (nmol4-MU min -1mg -1Albumen) |
| CK treatment group | 9.37±0.98 |
| H 2O treatment group | 11.18±1.09 |
| Cd treatment group | 37.54±1.13 |
| Cu treatment group | 31.56±1.57 |
| Zn treatment group | 38.13±2.58 |
Note: in table, numerical value is mean+SD.
Above-mentioned experiment proves that AtMT1a promotor has tissue expression specificity and is subject to the stress-inducing of the divalent-metal ions such as cadmium, copper, zinc.This lays a good foundation to utilizing this promotor to carry out genetically engineered improvement to farm crop further.
Embodiment 2, cultivation heavy metal pollution of soil early warning transgenic plant
1, the structure of the plant expression vector of AtMT1a promoters driven RFP gene
With the genomic dna of Ler Arabidopsis thaliana ecotype blade for template, carry out pcr amplification with P3:5 '-CATAGTTACGTAATCTTAAC-3 ' and P4:5 '-CCGCAAGTTTTAGTTACGTA-3 ' as primer, check order after the pcr amplification product obtained is connected with pMD19-T cloning vector (TAKARA company).Sequencing result is shown the recombinant vectors called after pMD-AtMT1a containing the DNA molecular shown in the 1-1140 position of SEQIDNo.1.Wherein, SEQIDNo.1 is made up of 1140 Nucleotide, is the nucleotide sequence of AtMT1a promotor.
Intermediate carrier pMD-AtMT1a and plant expression vector pBI-121 is cut with enzyme while of HindIII and XbaI two Restriction Enzymes, recovery AtMT1a promoter fragment is cut large fragment with the enzyme of pBI-121 and is connected, the recombinant vectors pBI-AtMT1a-Gus that between HindIII and the XbaI site of the AtMT1a promotor replacement pBI-121 of acquisition SEQIDNo.1, fragment obtains; With BamHI and SacI two restriction enzymes, simultaneously enzyme cuts the RFP gene shown in SEQIDNo.2 that BamHI and SacI restriction enzyme site is carried at pBI-AtMT1a-Gus and two ends, recovery RFP gene endonuclease bamhi is cut large fragment with pBI-AtMT1a-Gus enzyme and is connected, the plant expression vector pBI-AtMT1a-RFP (Fig. 5) of the AtMT1a promoters driven RFP gene that fragment obtains between BamHI and the SacI restriction enzyme site of the RFP gene coded sequence replacement pBI-AtMT1a-Gus shown in acquisition SEQIDNo.2 9-686 position.Red fluorescent protein expression casette containing SEQIDNo.3 in pBI-AtMT1a-RFP, in SEQIDNo.3,7-1146 position is AtMT1a promotor, and 1159-1836 position is RFP gene, and 1843-2097 position is Tnos terminator.The red fluorescent protein of the RFP genes encoding SEQIDNo.4 of SEQIDNo.3 1159-1836 position.
2, heavy metal pollution of soil early warning transgenic arabidopsis is cultivated
2.1, conversion and kantlex screening
According to the colored method pBI-AtMT1a-RFP that is stained with of document (Clough and Bent, 1998) and embodiment 1, genetic transformation is carried out to Ler Arabidopsis thaliana ecotype.Spray at the petal of Arabidopis thaliana with restructuring agrobacterium tumefaciens lba4404/pBI-AtMT1a-RFP (pBI-AtMT1a-RFP being proceeded to the recombinant bacterium that agrobacterium tumefaciens lba4404 competent cell obtains) the bacterium liquid containing plant expression vector pBI-AtMT1a-RFP; After one month, collect pBI-AtMT1a-RFP and transform (T in the present age
0generation) T that ties of Arabidopsis plant
1the seed in generation, obtains turning pBI-AtMT1a-RFPT
1for Arabidopis thaliana seed.
Get and turn pBI-AtMT1a-RFPT
1be layered on screening culture medium (1/2MS+50 μ g/ml kantlex) upper cultivation 10 days (Fig. 6) for Arabidopis thaliana seed, select root can the plantlet of transplant of normal growth in flowerpot, cultivate in 22 DEG C of greenhouses.What finally have the acquisition 35 strain kantlex positive altogether turns pBI-AtMT1a-RFPT
1for Arabidopsis thaliana Seedlings.
2.2, pBI-AtMT1a-RFPT is turned
1pCR for Arabidopis thaliana detects
The 35 strain kantlex positives 2.1 turn pBI-AtMT1a-RFPT
1pBI-AtMT1a-RFPT is turned for random selecting in the Arabidopsis thaliana Seedlings 20 strain kantlex positive
1pCR detection is carried out: with the genomic dna of blade for template for Arabidopsis thaliana Seedlings, special primer by AtMT1a promotor: P5:5 '-GCGATAGTTACTCTTCTTGCGT-3 ', with the special primer of red fluorescent protein gene: P6:5 '-GTCCCTCGGTTCTTTCATAC-3 ' carries out pcr amplification, electrophoresis detection pcr amplification product.Wherein, using the positive control that recombinant plasmid pBI-AtMT1a-RFP detects as PCR for template.
PCR detected result (Fig. 7) shows: turn pBI-AtMT1a-RFPT in the 20 strain kantlex positives
1for in Arabidopsis thaliana Seedlings, what have the 16 strain kantlex positives turns pBI-AtMT1a-RFPT
1be positive (PCR primer is 972bp) for Arabidopsis thaliana Seedlings PCR detected result.Which illustrate Arabidopis thaliana to be stained with colored method for transformation to be combined kantlex screening method be highly effective, transformation efficiency is about 80%.
This 16 strain PCR positive turned pBI-AtMT1a-RFPT
1strain for Arabidopis thaliana be called Line-1, Line-2 ..., Line-16.
2.3 turns of pBI-AtMT1a-RFPT
2northern for Arabidopis thaliana detects
That gathers in the crops the 16 strain PCR positives of 2.2 respectively turns pBI-AtMT1a-RFPT
1for the seed of Arabidopis thaliana, its seed is continued plantation, obtain and turn pBI-AtMT1a-RFPT
2for the plant of Arabidopis thaliana.
PBI-AtMT1a-RFPT is turned in order to detect
2can the red fluorescent protein gene for Arabidopis thaliana at transcriptional level correction, respectively with this Line-1, Line-2 ..., Line-16 these 16 turns pBI-AtMT1a-RFPT
2blade for Arabidopis thaliana is material extraction total serum IgE, carries out Northern hybridization qualification with the RFP gene shown in SEQIDNo.2 9-686 position as probe.Qualification result shows: T
2red fluorescent protein gene for transgenic arabidopsis all can be expressed at transcriptional level, but expression level presents certain otherness (Fig. 8).Wherein, the red fluorescent protein gene of line-1, line-4, line-5, line-6, line-7, line-8 and line-13 strain is expressed comparatively strong at transcriptional level, so gather in the crops the seed of the positive seedling of this 7 strain respectively, obtain turning pBI-AtMT1a-RFPT
3for Arabidopis thaliana seed.
2.4 turns of pBI-AtMT1a-RFPT
3for the checking of Arabidopis thaliana as heavy metal pollution of soil early warning transgenic plant
Line-1, line-4, line-5, line-6, line-7, line-8 and line-13 strain of getting 2.3 results turns pBI-AtMT1a-RFPT
3for Arabidopis thaliana seed, each strain all establishes following four treatment group: 0 μm of ol/LCd treatment group, 10 μm of ol/LCd treatment group, 20 μm of ol/LCd treatment group, 100 μm of ol/LCd treatment group.0 μm of ol/LCd treatment group turned pBI-AtMT1a-RFPT
3be implanted on 1/2MS substratum for Arabidopis thaliana seed, 10 μm of ol/LCd treatment group are turned pBI-AtMT1a-RFPT
31/2MS+10 μm of ol/LCd is implanted in for Arabidopis thaliana seed
2+on substratum, 20 μm of ol/LCd treatment group are turned pBI-AtMT1a-RFPT
31/2MS+20 μm of ol/LCd is implanted in for Arabidopis thaliana seed
2+on substratum, 100 μm of ol/LCd treatment group are turned pBI-AtMT1a-RFPT
31/2MS+100 μm of ol/LCd is implanted in for Arabidopis thaliana seed
2+on substratum.Cultivate after 14 days at identical conditions, get root and blade respectively, after rinsing with 1/2MS liquid nutrient medium, adopt laser confocal microscope to detect immediately, excitation wavelength is 561nm, and sensing range is 570-630nm.Three repetitions are established in experiment, repeat each treatment group 3 strain Arabidopis thaliana at every turn.Result shows at 0 μm of ol/LCd
2+environment in line-1, line-4, line-5, line-6, line-7, line-8 and line-13 strain of growing turn pBI-AtMT1a-RFPT
3(in Fig. 9 f), 10 μm of ol/LCd are being more than or equal to for all can't detect red fluorescence in Arabidopsis leaf
2+environment (10 μm of ol/LCd
2+, 20 μm of ol/LCd
2+with 100 μm of ol/LCd
2+environment) in growth line-1, line-4, line-5, line-6, line-7, line-8 and line-13 strain turn pBI-AtMT1a-RFPT
3for all detecting red fluorescence (in Fig. 9 a-c) in Arabidopsis leaf.In blade, RFP gene is mainly expressed in the vacuole chamber that central authorities are large, further raising magnification can clearly be observed, and RFP gene does not navigate on vacuole skin and other plasmalemmas, but to be positioned in vacuole chamber (d and e) in Fig. 9.
At 0 μm of ol/LCd
2+environment in line-1, line-4, line-5, line-6, line-7, line-8 and line-13 strain of growing turn pBI-AtMT1a-RFPT
3for all can't detect red fluorescence (Figure 10) in the root of Arabidopis thaliana, at 10 μm of ol/LCd
2+environment in line-1, line-4, line-5, line-6, line-7, line-8 and line-13 strain of growing turn pBI-AtMT1a-RFPT
3red fluorescence (Figure 11 and Figure 12) is all detected in vacuole chamber for the root of Arabidopis thaliana.
Above, 1/2MS+10 μm of ol/LCd
2+substratum adds CdCl in 1/2MS substratum
2the substratum obtained, 1/2MS+10 μm of ol/LCd
2+cd in substratum
2+concentration be 10 μm of ol/L.1/2MS+20 μm of ol/LCd
2+substratum adds CdCl in 1/2MS substratum
2the substratum obtained, 1/2MS+20 μm of ol/LCd
2+cd in substratum
2+concentration be 20 μm of ol/L.1/2MS+100 μm of ol/LCd
2+substratum adds CdCl in 1/2MS substratum
2the substratum obtained, 1/2MS+100 μm of ol/LCd
2+cd in substratum
2+concentration be 100 μm of ol/L.
The above results shows, the transfer-gen plant carrying AtMT1a promoters driven RFP gene can under there is the condition of 10 μm of more than ol/L cadmium metal ions in environment, inspire danger signal, illustrate that AtMT1a promotor and the expression cassette by AtMT1a promoters driven RFP genetic expression can be used for cultivating heavy metal-polluted soil (as Cd
2+) pollution prewarning transgenic plant.
Although above the present invention is described in detail with a general description of the specific embodiments, on basis of the present invention, can make some modifications or improvements it, this will be apparent to those skilled in the art.Therefore, these modifications or improvements without departing from theon the basis of the spirit of the present invention, all belong to the scope of protection of present invention.
Claims (7)
1. nucleotide sequence is the DNA molecular of SEQIDNo.1.
2. the expression cassette containing DNA molecular described in claim 1.
3. the recombinant vectors containing DNA molecular described in claim 1, or the recombinant vectors containing expression cassette described in claim 2.
4. containing the recombinant microorganism of DNA molecular, the recombinant microorganism containing expression cassette described in claim 2 or the recombinant microorganism containing recombinant vectors described in claim 3 described in claim 1.
5. containing the transgenic cell line of DNA molecular, the transgenic cell line containing expression cassette described in claim 2 or the transgenic cell line containing recombinant vectors described in claim 3 described in claim 1.
6. DNA molecular according to claim 1 is at Cd
2+coerce the application that lower startup goal gene is expressed in plant.
7. DNA molecular according to claim 1 is at cultivation soil Cd
2+application in pollution prewarning transgenic plant.
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| CN101845437A (en) * | 2010-04-19 | 2010-09-29 | 清华大学 | Promoter with properties of inducing and organizing specific expression |
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| CN101845437A (en) * | 2010-04-19 | 2010-09-29 | 清华大学 | Promoter with properties of inducing and organizing specific expression |
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| Title |
|---|
| Characterization of the Arabidopsis metallothionein gene family：tissue-specific expression and induction during senescence and in response to copper;Woei-Jiun Guo等;《New Phytologist》;20031231;第159卷;371-375 * |
| Structure，organization and expression of the metallothionein gene family in Arabidopsis;Jianmin Zhou等;《Mol Gen Genet》;19951231;第248卷;322 * |
| U11253;登录号;《NCBI Genbank》;19951130;全文 * |
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