Drought-resistant transcription factor PbrERF109, preparation method and application of transcription factor PbrERF109, encoded protein and application of encoded protein
A transcription factor and protein technology, applied in the field of plant genetic engineering, can solve the problems of unreported ERF transcription factors such as drought resistance, and achieve the effect of enhancing reactive oxygen species scavenging ability and improving drought resistance ability.
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[0038] In the present invention, the preparation method of the drought-resistant transcription factor PbrERF109 comprises the following steps:
[0039] Using pear cDNA as a template, the drought-resistant transcription factor PbrERF109 was obtained by PCR amplification with transcription factor primers;
[0040] The transcription factor primer pair includes a transcription factor upstream primer and a transcription factor downstream primer, the transcription factor upstream primer has the nucleotide sequence shown in SEQ ID No.3, and the transcription factor downstream primer has the nucleotide sequence shown in SEQ ID No.4 The nucleotide sequence shown.
[0041] In the present invention, the method for preparing pear cDNA preferably comprises: extracting RNA from leaves of Pear pear, and reverse-transcribing the obtained RNA to obtain cDNA. The method for extracting RNA is not particularly limited in the present invention, and the method for extracting plant RNA conventional...
Embodiment 1
[0066] Cloning and expression analysis of PbrERF109 gene
[0067] RNA was extracted from the leaves of Duli pear under drought and dehydration treatment, and cDNA was obtained by reverse transcription. In the present invention, after obtaining the cNDA, the obtained cDNA is used as a template, and a specific transcription factor primer pair is used to obtain the drought-resistant transcription factor PbrERF109, the specific sequence of which is shown in SEQ ID No.1.
[0068] For RNA extraction, Plant Total RNA Isolation Kit Plus (Foregene, RE-05022) was used, and the operation instructions provided by the kit were followed. First-strand cDNA was synthesized using First Script Strand cDNASynthesis SuperMix (Transgene, AE301-02) reverse transcription kit (operated according to the instructions provided by the kit).
[0069] The primer pair for amplifying the drought-resistant transcription factor PbrERF109 is: Forward primer: PbrERF109 Forward, 5'-GA AGATCT TATGCCCTTCCATGCGAA...
Embodiment 2
[0079] Analysis of subcellular localization and transcriptional activation of PbrERF109 gene
[0080] Since the PbrERF109 gene is a transcription factor, the present invention uses tobacco mesophyll cells to study the subcellular localization of the PbrERF109 gene. The entire ORF reading frame of the PbrERF109 gene was amplified by RT-PCR, and two restriction sites, XbaI and BamHI, were added at both ends of the amplification primer. The amplification primer is (forward primer PbrERF109-F2: 5'- TCTAGA ATGCCCTTCCATGCGAATCGGATA-3'(SEQ ID No.11); reverse primer PbrERF109-R2: 5'- GGATCCCCTAGTTCGTGGATAACCA-3' (SEQ ID No.12)), firstly digest the amplified product. In the present invention, the temperature for the double digestion of the pear drought-induced transcription factor PbrERF109 is 37° C., and the time for the double digestion is 12 hours; the total volume of the double digestion system is 20 μl, including the PCR purified product of the pear drought-induced transcripti...
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