Method for improving fertility of indica-japonica rice hybrids by virtue of LRK1 gene transformation
A technology for gene transformation and rice, applied in the field of transgenic, can solve the problems such as indica-japonica rice that have not yet been seen, and achieve the effects of overcoming the sterile characteristics of indica-japonica hybridization, low cost, and wide compatibility.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0034] Example 1 Functional verification of LRK1 gene
[0035] (1) Construction of LRK1 gene expression vector
[0036] Using pCAMBIA1304 as the expression vector, the Dongxiang wild rice LRK1 gene was inserted into the downstream of the 35S-type promoter of the pCAMBIA1304 vector; the structure of the expression vector containing the LRK1 gene is as follows: figure 1 shown;
[0037] (2) LRK1 gene transformation experiments and results
[0038] 9311, one of the main parents of domestic super hybrid rice, was used as the transgenic receptor; the mature seeds of 9311 were dehulled and sterilized and then inoculated on the dedifferentiated plant tissue culture medium to induce callus; after 2-3 weeks of callus induction, The purified pCAMBIA1304 plasmid DNA containing the LRK1 gene was introduced into 9311 callus cells by the method of microprojectile bombardment; the resistant cell lines were screened by continuous culture on MS medium supplemented with 30 ppm hygromycin for 3...
Embodiment 2
[0046] Example 2 The method of transforming indica rice 9311 with rice LRK1 gene
[0047] (1) Select the full-length ORF segment of LRK1 (see sequence listing), amplify it from Dongxiang wild rice by PCR method, and clone it into the plant expression vector pCAMBIA1304 with a synthetic insert to obtain the LRK1 expression vector pCAMBIA1304 / LRK1;
[0048] (2) Induced rice callus medium
[0049] 1) Induction and subculture medium: MS+2mg / L2,4-D;
[0050] 2) Hypertonic medium: MS+2mg / L2,4-D+46.67g / L sorbitol+46.67g / L mannitol;
[0051] 3) The first round of screening medium: MS+2mg / L2,4-D+30mg / L hygromycin;
[0052] 4) The second round of screening medium: MS+2mg / L2,4-D+50mg / L hygromycin;
[0053] 5) Differentiation medium: MS+3mg / L6-BA+0.5mg / LNAA+50mg / L hygromycin;
[0054] 6) Medium for rooting and strong seedlings: 1 / 2MS+0.1mg / LNAA;
[0055] Note: ①The above medium contains 30g / L sucrose+2.5g / L agar, pH 5.8; ②The culture conditions for callus induction, subculture and sc...
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