Soybean bHLH transcription factor and encoding gene and application thereof
A technology that encodes genes and transcription factors, applied in the field of genetic engineering, can solve problems that affect plant growth and development, endanger human health, etc., and achieve the effects of reducing cadmium content, reducing harm, and improving tolerance
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Embodiment 1
[0031] Example 1: soybean GmORG3 Gene cloning and subcellular localization
[0032] Cloning of Soybean by Combining Bioinformatics and Conventional Polymerase Chain Reaction (PCR) GmORG3 The DNA sequence, the specific method is:
[0033] Soybean roots were used as experimental materials, and total RNA was extracted using SVTotalRNAlysis Kit (Promega, USA). The first strand of cDNA was synthesized according to the method provided by TaKaRa Company (PrimeScriptTMReverseTranscriptase), and used as a template for PCR amplification. According to known in NCBI GmORG3 Sequence design a pair of primers (primers were synthesized by Shanghai Invitrogen Company):
[0034] P1: 5'-ATGGTTGCTTTGTTTTTCCCCT-3',
[0035] P2: 5'-TTAGAAAATCCTTTGCTTCTC-3'.
[0036] Amplified by RT-PCR GmORG3 The complete ORF fragment of the gene. 25μl PCR reaction system: 2.5μl containing MgCl 210×PCR buffer, 1.0 μl forward and reverse 10 μM primers, 1.0 μl 10 mM dNTP (deoxynucleotide mixture), 2.0 μl cDN...
Embodiment 2
[0038] Example 2: GmORG3 Transcript spatiotemporal distribution and Cd stress on GmORG3 Effects on Gene Expression
[0039] The tissue distribution of GmORG3 in soybean plants was detected by semi-quantitative PCR, and the following measures were taken to ensure the reliability of the detection results: the contamination of a small amount of genomic DNA that may exist in the total RNA extracted by digestion with amplification grade DNaseI was To check whether the genomic DNA is completely eliminated, a part of the total RNA sample digested with DNaseI can be taken out for conventional PCR reaction. When no amplified band is found, the reverse transcription step is carried out. At the same time, in order to further verify the band amplified by real-time quantitative PCR belt is GmORG3 , PCR products were gel-cut and recovered for sequencing. The specific method is as follows: extract total RNA from soybean roots, stems, leaves, flowers and pods in different growth stages as ...
Embodiment 3
[0051] Example 3: GmORG3 Construction of yeast expression vector and detection of Cd tolerance in transgenic yeast
[0052] (1) Construction of expression vector
[0053] by GmORG3 The full-length sequence of the cDNA was used as a template, and the primer (synthesized by Shanghai Biological Engineering Co., Ltd.) containing a restriction site: P5: 5′-TCC CCCGGG ATGGTTGCTTTGTTTTTCCCCT-3′ (underlined bases are restriction endonuclease SmaI recognition sites) and P6: 5′-CG GAATTC Under the guidance of TTAGAAAAATCCTTTGCTTCTC-3′ (the underlined base is the restriction endonuclease EcoRI recognition site), PCR amplified the 5’ end with SmaI recognition site and the 3’ end with EcoRI recognition site GmORG3 cDNA full-length sequence. After the reaction, the PCR amplification product was detected by 1.0% agarose gel electrophoresis, and the target fragment of about 800bp was recovered and purified, digested with SmaI and EcoRI, and then combined with the vector p424GPD ( Figu...
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