Alfalfa draught resistant gene MsTHI1 and encoded protein and application thereof
A kind of technology of alfalfa and gene, applied in the direction of application, genetic engineering, plant genetic improvement, etc., can solve the problem of weak drought resistance and achieve the effect of improving drought resistance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0068] Example 1 Acquisition of MsTHI1 gene from alfalfa
[0069] (1) Extraction of total RNA and its reverse transcription
[0070] Plant alfalfa No. Longmu 801 in vermiculite, extract total RNA from alfalfa seedlings with a plant total RNA extraction kit purchased from Kangwei Century Biotechnology Co., Ltd., detect its integrity with agarose gel, and measure it with a micro-spectrophotometer concentration. The reverse transcription of RNA was carried out with HiScript II Q Select RT SuperMix for qPCR (+gDNAwiper) kit (Vazyme, China), and the quality of cDNA was identified by PCR with Taq enzyme (Kangwei Century). The reaction system is shown in Table 2.
[0071] Table 2 Reverse transcription reaction system
[0072]
[0073] Reverse transcription primer sequence:
[0074] Upstream primer: 5'-TTTGAGACTTTCAATGTGCCCGCC-3' (Sequence Listing ID NO.3)
[0075] Downstream primer 5'-TAGCATGTGGGAGTGCATAACCCT-3' (Sequence Listing ID NO.4)
[0076] The reverse transcription re...
Embodiment 2
[0092] Example 2 Real-time fluorescent quantitative PCR detection gene expression characteristics in alfalfa under adversity stress conditions
[0093] Select alfalfa seeds with full grains, cultivate them in vermiculite, and water them with 1 / 10 Hoagland nutrient solution. When the seeds were 4 weeks old, the plants were treated with 15% PEG-6000, 150mmol / L NaCl, 150mmol / L NaHCO 3 , 4°C stress treatment, the treatment time was 0h (CK), 3h, 6h, 12h, 24h, 48h, and each treatment set 3 repetitions. The leaves, stems and roots of the plants were taken, frozen in liquid nitrogen, and stored at -80°C. Design fluorescent quantitative expression primers based on the full-length cDNA sequence:
[0094] Upstream primer 5'-TGTGGCCATGATGGTCCTTT-3' (Sequence Listing ID NO.7)
[0095] Downstream primer 5'-TCCTCGGCAGTGTTCATGTC-3' (Sequence Listing ID NO.8)
[0096] Internal reference gene primers:
[0097] Upstream primer: 5'-GGCTGCCATCAAGGAGGAAT-3' (Sequence Listing ID NO.9)
[0098]...
Embodiment 3
[0110] The subcellular localization of embodiment 3MsTHI1 gene
[0111] By constructing a tobacco transient expression vector, use GV3101 Agrobacterium (purchased from Beijing Bomaide Biotechnology Co., Ltd.) to inject into Nicotiana tabacum L (provided by Plant Genetic Engineering and Molecular Biology Experiment, College of Biological Sciences, Northeast Agricultural University) In , transient expression was carried out, and the expression position of MsTHI1 gene was observed under confocal electron microscopy.
[0112] The construction method of tobacco transient expression vector is:
[0113] Primers were designed based on the complete open reading frame of the MsTHI1 gene:
[0114] Upstream primers:
[0115] 5'-CGGGGGACTCTTGACGAGCTCATGACGACGTCGTTCGCC-3' (Sequence Listing ID NO.11)
[0116] Downstream primers:
[0117] 5'-CATGTCGACTCTAGAGGATCCAAATTCACCTTTTCCATTTTGGTT-3' (Sequence Listing ID NO.12)
[0118] The PCR amplification product in Example 1 was ligated with th...
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