Solanum torvum StoWRKY6 gene and expression vector and applications thereof
A technology of expression vector and wild eggplant, applied in application, genetic engineering, plant gene improvement, etc., can solve problems such as low disease resistance and yield loss
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0035] The cloning of embodiment 1StoWRKY6 gene
[0036] Total RNA was extracted from wild eggplant Solanum torvum Swartz by Trizol kit. The first strand of cDNA was synthesized using the reverse transcriptase system of Bao Bioengineering Company.
[0037] Design intermediate conserved sequence primer P1 (forward primer W1: 5'-ATATGGGTAACTCATCGAMTSATC-3' (SEQ ID NO.3) (M stands for A or C; S stands for C or G) and reverse primer W2: 5'-TGTTTTTGTCCATCTTGTCC- 3' (SEQ ID NO.4)), the middle conserved region of StoWRKY6 cDNA was obtained by PCR amplification of the first strand of synthetic cDNA. After electrophoresis on 1.0% agarose, the PCR product was recovered with the gel recovery kit of Bao Bio Company, connected to pMD18-T Vector, transformed into Escherichia coli DH5α, single clone was detected by PCR, and the positive clone was sent to BGI for sequencing. The middle fragment of about 382bp.
[0038] According to the blastn alignment results of the wild eggplant StoWRKY6...
Embodiment 2
[0039] Example 2 StoWRKY6 Gene Tissue Expression Analysis
[0040] Total RNA was extracted from wild eggplant roots, stems, leaves, senescent leaves, mature leaves, and young leaves at the 6-leaf stage, and the cDNA obtained after reverse transcription was used as a template. ID NO.7) and reverse primer 5'-CAAAATTCCAAAGACCCTCC-3' (SEQ ID NO.8)), semi-quantitative RT-PCR was performed to detect the expression of StoWRKY6 gene in different tissues of wild eggplant. PCR amplification conditions Pre-denaturation at 94°C for 4min, followed by 30 cycles at 94°C for 40s; 58°C for 40s; 72°C for 30s, and finally 72°C for 10min. PCR products were spotted and detected by 1% agarose gel electrophoresis. The internal reference used the constitutively expressed EF1α gene, and the primers were EF1α1:5′-GTGGTGGAGTCAATAATGAGGAC-3′ (SEQ ID NO.9) and EF1α2:5′-TCGACAACAGAAACATCAGCAGT-3′ (SEQ ID NO.10). The PCR conditions were: 94°C pre-denaturation for 4min, then 94°C for 40s; 58°C for 30s; 72°...
Embodiment 3
[0041] Semi-quantitative analysis of StoWRKY6 gene expression under embodiment 3SA, JA and Verticillium dahliae induction
[0042] To study the expression of StoWRKY6 under the stress of salicylic acid (SA) and jasmonic acid (JA). The healthy and disease-free 6-leaf stage seedlings were taken for chemical treatment as follows: the final concentrations of salicylic acid and jasmonic acid were 300 mM and 200 μM, respectively, and the control treatment was Tween20 / water to make it similar to the corresponding chemical treatment conditions. The leaves of all plants were sampled at 0h, 2h, 4h, 12h, and 48h after treatment, and all were frozen and stored in a -70 refrigerator. RNA was extracted for semi-quantitative reverse transcription PCR (RT-PCR) analysis, and the constitutively expressed EF1α gene was used as an internal reference. Semi-quantitative RT-PCR using primer QN was used to detect the expression of StoWRKY6 gene in wild eggplant plants under SA and JA treatment, resp...
PUM
Property | Measurement | Unit |
---|---|---|
molecular weight | aaaaa | aaaaa |
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