Gene CdERF1 of Cynodon dactylon significantly induced by low temperature and application thereof
A low-temperature induction, bermudagrass technology, applied in application, genetic engineering, plant genetic improvement, etc., can solve the problems of weak research on the molecular mechanism of bermudagrass cold resistance, unclear genetic background of bermudagrass, lack of original cold resistance genes, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 2
[0058] 2. Example 2: Molecular Cloning of Bermudagrass CdERF1 Gene
[0059] Sequencing found that the 5' end of the ERF2 sequence started from the start codon ATG, followed by 3'RACE PCR amplification; according to TaKaRa 3'-Full RACE Core Set with PrimeScript TM According to the requirements of the RTase manual, 3 specific primers were designed for 3’-RACE, and the primers are as follows:
[0060] ERF2-3'RACEouter, 5'-CTCGTGGATTCTCCAAATGGTGCA-3';
[0061] ERF2-3'RACEinner1, 5'-AGGACGAGAGAACCCAGTATTACC-3';
[0062] ERF2-3'RACEinner2,5'-ACCAAGCGTAGAAAACGGCACAGA-3';
[0063] The principle of 3'-RACE is: use Total RNA as a template, use 3'RACE Adapter primers, perform reverse transcription under the action of reverse transcriptase PrimeScript Reverse Transcriptase, and synthesize the first standard cDNA; use the upstream outer specific primer ( ERF2-3'RACEouter) and 3'RACE OuterPrimer for the first round of PCR amplification; if the first round of PCR reaction fails to obtain ...
Embodiment 3
[0068] 3. Example 3: Analysis of the expression profile of the transcription factor gene CdERF1 under stress
[0069] ERF transcription factors respond to a wide range of biotic and abiotic stresses, such as low temperature, drought, high salinity, pests and mechanical damage, etc. can induce the expression of ERF transcription factor genes, and different ERF transcription factors show different behaviors under different stress conditions. expression pattern; the primer sequences used in this experiment are as follows:
[0070] CdERF1-q up: 5'-ACTGCAGAGGTACACCT-3';
[0071] CdERF1-q dn: 5'-GAAGAGCCACCACCATT-3';
[0072] CdACT2up: 5'-TCTGAAGGGTAAGTAGAGTAG-3';
[0073] CdACT2dn: 5'-ACTCAGCACATTCCAGCAGAT-3'.
[0074] Mature bermudagrass grown for 2 months were given low temperature (4°C), drought (25% PEG), high salt (200 mM NaCl), abscisic acid (100 μM ABA), ethylene (100 μM ACC) and jasmonic acid (100 μM JA), etc. Different treatments; the leaves of the seedlings were cut a...
Embodiment 6
[0120] 6. Embodiment 6: Cultivation and genetic transformation of Arabidopsis thaliana
[0121] 1) Culture of Arabidopsis
[0122] A. Put a little Arabidopsis seeds into a centrifuge tube, add sodium hypochlorite to treat for 5-6 minutes, absorb the sodium hypochlorite and wash the seeds with sterile water 4-6 times;
[0123] B. Spread the seeds on the surface of MS solid medium, and disperse the seeds evenly; place the culture dish at 4°C for 3 days, then transfer it to the Arabidopsis room (22°C) for germination and culture for 10 days, and then transplant ;
[0124] C, plant about 6-9 Arabidopsis thaliana in the sterilized nutrient soil of every pot;
[0125] D. When Arabidopsis thaliana is bolted, the main stem is cut off from the base, so as to promote the growth of side branches and bolting and flowering, and then be used for transformation;
[0126] 2) Transfection of Arabidopsis thaliana by soaking flowers
[0127] A, select Arabidopsis thaliana with more flowering...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com