Plant resistance related protein MAG, and coding gene and application thereof

A gene and protein technology, applied to plant resistance-related protein MAG and its encoding gene and application field, can solve the problems of increasing salicylic acid, not yet found, not found, etc., to achieve the effect of enhancing disease resistance

Active Publication Date: 2013-08-21
FUJIAN SANAN SINO SCI PHOTOBIOTECH CO LTD
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

So far, it has only been found that ETHYLENEINSENSITIVE3 (EIN3) and EIN3-LIKE1 can directly bind to the ICS1 promoter of the key SA biosynthesis gene, and negatively regulate the synthesis level of SA. It has not been found that ICS1 gene expression can be promoted by positively inducing the ICS1 promoter. proteins that increase the level of salicylic acid synthesis
In addition, studies have found that SAR Deficient 1 (SARD1) and CBP60g proteins are important factors in inducing ICS1 gene expression and SA synthesis, but failed to find more positive induction of ICS1 promoter to promote ICS1 gene expression, thereby increasing the level of salicylic acid synthesis protein

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Plant resistance related protein MAG, and coding gene and application thereof
  • Plant resistance related protein MAG, and coding gene and application thereof
  • Plant resistance related protein MAG, and coding gene and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0062] Embodiment 1, the acquisition of MAG protein and its coding gene

[0063] 1. According to the existing NCBI database and literature, set a pair of primers as follows:

[0064] F1 (forward primer): 5'- TCTAGA GTCAACGTCGCATACTTTTGAA-3' (underlined XbaI restriction recognition sequence);

[0065] R1 (reverse primer): 5'- GGATCC CGAGAGGTTTAAGAGGTGTTCTTA-3' (underlined BamHI restriction recognition sequence).

[0066] 2. Genomic DNA was extracted from leaves of Arabidopsis thaliana ecotype Columbia.

[0067] 3. Using genomic DNA as a template, use the primer pair designed in step 1, and perform PCR amplification with PrimeSTAR HS high-fidelity enzyme from TaKaRa Company.

[0068] 4. The PCR amplification product is sequenced, as shown in sequence 2 of the sequence listing.

[0069] The protein shown in Sequence 1 of the Sequence Listing is named MAG protein. The gene encoding the MAG protein is named as the MAG gene, and its genomic DNA is shown in Sequence 2 of the ...

Embodiment 2

[0070] Embodiment 2, the cloning of each gene and the construction of its recombinant expression vector

[0071] 1. Obtaining of MAG gene and construction of recombinant plasmid 326-MAG-FLAG

[0072] 1. Genomic DNA was extracted from leaves of Arabidopsis thaliana ecotype Columbia.

[0073] 2. Using the genomic DNA in step 1 as a template, use the primer pair composed of F1 and R1 to carry out PCR amplification under the action of TaKaRa's PrimeSTAR HS high-fidelity enzyme to obtain PCR amplification products. The agarose gel electrophoresis of the PCR amplification product is shown in figure 1 (M represents a nucleotide marker, which is DL2000 from TaKaRa Company).

[0074] 3. The PCR amplification product of step 2 was double-digested with restriction enzymes XbaI and BamHI, and the digested product was recovered.

[0075] 4. The 326-FLAG expression vector was double digested with restriction enzymes XbaI and BamHI, and the vector backbone of about 3827 bp was recovered.

...

Embodiment 3

[0097] Embodiment 3, the application of MAG gene in inducing ICS1 gene promoter (ProAtICS1) to start gene expression

[0098] 1. Transient expression of recombinant plasmids in Arabidopsis leaf protoplasts

[0099] The recombinant plasmid 326-MAG-FLAG and recombinant plasmid 326-Pro constructed in Example 2 AtICS1 ::GFP co-transformed Arabidopsis protoplasts (recombinant plasmid 326-T 7 -FLC is used as a negative control of the recombinant plasmid 326-MAG-FLAG; the 326-FLAG expression vector is used as another negative control of the recombinant plasmid 326-MAG-FLAG), the specific steps are as follows:

[0100] 1. Germinate Colombian ecotype Arabidopsis seeds on MS medium, transplant them into soil when the roots grow to 1-3 cm, and cultivate them in a greenhouse at 23° C. (12 hours of light per day, light intensity of 150 μE).

[0101] 2. Add 20ml of double distilled water to a 90mm petri dish, then add 1.82g of D-mannitol and dissolve it.

[0102] 3. Take the unbolted lea...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a plant resistance related protein MAG, and a coding gene and application thereof. The protein disclosed by the invention is named MAG protein, comes from Arabidopsis thaliana, and is (a) a protein composed of an amino acid sequence shown in sequence 1; or (b) a protein derived from sequence 1, which is formed by the substitution and / or deletion and / or addition of one or more amino acid residues in the amino acid sequence shown in sequence 1 and has any function of inducing the activation of an ICS1 gene promoter, inducing the activation of a PR1 gene promoter, being related to the synthesis of salicylic acid in plants or being related to the plant resistance. The MAG protein disclosed by the invention can enhance the disease resistance of plants by regulating and controlling the synthesis of salicylic acid in the plants. The invention has an important value for the cultivation of disease-resistant plants.

Description

technical field [0001] The invention relates to a plant resistance related protein MAG, its encoding gene and application. Background technique [0002] Plants often suffer from various diseases in the process of cultivation and production. Some diseases pose a great threat to plant growth and seriously damage the yield and quality of crops. For plant diseases, at present, the main measures are to control them with drugs. Recently, people have begun to use abiotic inducers to induce plant disease resistance, and have been widely used in many important crops such as tobacco, potato, tomato, cucumber, bean, and rice. Although the effect of this measure is ideal, it is costly and pollutes the environment. Therefore, there is an urgent need to develop new biological means to improve the plant's own disease resistance. [0003] Systemic acquired resistance is a plant defense response that is induced when plants are attacked by pathogens and pests and can quickly spread to othe...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): C07K14/415C12N15/29C12N15/63C12N5/10C12N1/21C12N15/82A01H5/00
Inventor 金京波蔡斌林晓莉
Owner FUJIAN SANAN SINO SCI PHOTOBIOTECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products