Plants stress tolerance correlation transcription factor GmWRKY54, encoding gene and application thereof
A coding gene and gene technology, applied in soybean stress tolerance-related proteins and their coding genes and application fields, to achieve the effects of increasing yield, improving salt tolerance, and improving drought tolerance
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Embodiment 1
[0037] Example 1. Screening of soybean stress tolerance-related protein GmWRKY54 encoding gene and its cDNA clone
[0038] BLAST search was performed in the soybean EST database, and 64 WRKY-like gene fragments including the complete WRKY domain were clustered. 64 pairs of primers were designed according to the sequences of 64 WRKY gene fragments, and total RNA was extracted from soybean Kefeng 1 seedlings treated with 250mM NaCl, drought, -4°C and untreated for 3 weeks by conventional methods, and RT-RCR method was used to extract total RNA The relationship between the expression of 64 genes and stress treatment was determined. Screening resulted in a gene whose expression was induced by drought or salt stress and slightly induced by low temperature.
[0039] Total RNA was extracted from soybean Kefeng 1 seedlings, and cDNA was synthesized from RNA with reverse transcriptase. The primers were designed according to the gene sequence obtained from the above retrieval as follo...
Embodiment 2
[0043] Example 2, Expression characteristics of soybean GmWRKY54 gene under adversity stress treatment
[0044] Soybean Kefeng No. 1 seeds were planted in pots, and after 2 weeks of growth, the seedlings were taken and subjected to the following stress treatments: 1) salt stress treatment: the soybean seedlings were moved into 250 mM NaCl solution; 2) osmotic stress treatment: the soybean seedlings were moved into 20 %PEG solution; 3) low temperature stress treatment: the soybean seedlings were moved into 4°C aqueous solution. Illumination culture, samples were taken at 0, 0.5, 1, 3, 6, and 12 hours after the above-mentioned various treatments, and 1 g of fresh leaves were collected and ground in liquid nitrogen, suspended in 4 mol / L guanidine thiohydrogen, and the mixture was washed with acid phenol, Extract with chloroform, and add ethanol to the supernatant to precipitate to obtain total RNA. Northern analysis was performed using GmWRKY54 DNA as a probe (sequence 1 in the ...
Embodiment 3
[0046] Embodiment 3, use GmWRKY54 gene to cultivate salt-tolerant and drought-resistant plants
[0047] 1) Construction of GmWRKY54 expression vector pBin438-GmWRKY54
[0048] Using the cDNA obtained by reverse transcription of the total RNA of soybean Kefeng 1 as a template, GmWRKY54 (sequence 1 in the sequence listing) was amplified by PCR with specific primers containing BamHI and KpnI linker sequences; then BamHI and KpnI double-digested the PCR product , Recovered, GmWRKY54 was inserted forward into the plant binary expression vector pBin438 (Li Taiyuan, Tian Yingchuan, Qin Xiaofeng, etc. Research on efficient insect-resistant transgenic tobacco [J]. Chinese Science (Series B), 1994, 24 (3): 276- 282.) between the BamHI and KpnI restriction sites behind the CaMV 35S promoter, the recombinant vector pBin438-GmWRKY54 was obtained (Fig. 2).
[0049] The primer sequences are as follows:
[0050] 5’-ATC AGG ATC CAT GAC AGT AGA TCT GGT AGG-3’
[0051] 5'-GAT GGG TAC CTG ACA ...
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