An anthrax transcription factor csatf1 and its application
A transcription factor, anthracnose technology, applied in the application, fungicides, fungi and other directions, to achieve the effect of improving sterilization efficiency and sensitivity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] Cloning of embodiment 1 rubber tree anthracnose bacteria CsATF1 gene
[0025] According to the bZIP gene sequence of C. graminicola transcription factor (accession number XM008094996.1) obtained in NCBI, the homologous sequence was obtained by using the local BLAST method in the transcriptome database of Hevea anthracis HN08, and the primer pair CsATF1- F(5'-ATGGGAACTTCGCCGACCGAC-3') / CsATF1-R(5'-TCATGAGAAACGTCGCTGGA-3'), using the cDNA and DNA of C. siamense HN08 as templates, respectively amplified to obtain the target bands. Sequence analysis showed that the obtained sequence contained a complete coding open reading frame. The size of the DNA sequence is 1758bp, and the size of the cDNA sequence is 1611bp. The gene contains 2 introns, encodes 536 amino acids, and contains three Aft1 domains and a BRLZ (basic leucine zipper) domain, indicating that CsATF1 is bZIP ATF transcription factor in the transcription factor family. The gene was named CsATF1.
Embodiment 2
[0026] Example 2 Construction of CsATF1 gene knockout vector and acquisition of CsATF1 gene knockout mutant
[0027] Before and after the coding reading frame of the CsATF1 gene, design primer pairs CsATF1-UP-F / CsATF1-UP-R and CsATF1-D-F / CsATF1-D-R, use PCR amplification to obtain the upper arm sequence of the CsATF1 gene and the lower arm sequence after the C-terminal, using The method of homologous recombination, the upper arm and the lower arm sequence are joined into the vector pCX62-S, and the knockout vector pCX62-S-CsATF1 is obtained. See the diagram for details figure 1 .
[0028] The knockout vector pCX62-S-CsATF1 obtained from the above construction was introduced into protoplasts of Hevea anthracis HN08 by PEG-mediated protoplast transformation method, and screened by DCM medium containing chlorimuron-methyl (100 μg / mL) . A total of 3 batches were transformed and 159 transformants were obtained.
[0029] Genomic DNA sequences of 159 transformants were extracted ...
Embodiment 3
[0031] Example 3 CsATF1 gene deletion affects the sensitivity of fungi to the fungicide fludioxonil
[0032]In the medium containing different concentrations of fludioxonil, with the increase of fludioxonil concentration, the growth rate of the wild-type strain containing CsATF1 gene decreased gradually. However, in the CsATF1 gene deletion mutant, on the medium with the same concentration of fludioxonil, the growth rate of the mutant is greater than that of the wild type; see image 3 . The results indicated that the transcription factor CsATF1 could regulate the sensitivity of fungi to pyrrole agents such as fludioxonil, and the expression of this gene could increase the sensitivity of fungi such as anthrax to fludioxonil and other pyrrole agents.
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