Rice leaf rolling-associated protein OsMYB103L as well as encoding gene and application thereof
A gene and curling technology is applied to the rice leaf curling-related protein OsMYB103L and its encoding gene and application fields, so as to achieve the effect of improving plant type and increasing rice yield
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0040] Example 1. Discovery of rice leaf curl-related protein OsMYB103L and its encoding gene
[0041] Systematic reverse genetics research on several rice MYB genes pre-screened from the japonica rice variety Nipponbare (Oryza sativa L.subsp.japonica cv.Nipponbare), the main research strategy is to overexpress and / or RNAi the target gene analyze. A novel protein and its coding gene were discovered during phenotypic analysis of transgenic rice populations.
[0042] The protein shown in Sequence 1 of the Sequence Listing was named OsMYB103L protein (consisting of 359 amino acid residues). The domain analysis of OsMYB103L protein on the protein conservation domain analysis website showed that there were two tandem MYB DNA binding domains (R2 and R3) at its N-terminus. Systematic evolution of the OsMYB103L protein and the related R2R3MYB protein of Arabidopsis thalina (Arabidopsis thalina L.) revealed that it has the highest homology with AtMYB103 (At1g63910), and the two are hig...
Embodiment 2
[0044] Example 2. Functional verification of OsMYB103L protein as a transcription factor
[0045] 1. Localization of OsMYB103L protein in plant cells
[0046] Transcription factors generally perform their biological functions in the nucleus. In order to analyze the localization of the OsMYB103L protein in cells, the 3' end of the full-length ORF of the OsMYB103L gene (the DNA shown in Sequence 2 of the Sequence Listing without the stop codon) was combined with the binary vector pEZR(K)-LN (Brown et al , PNAS, 2005, 102:18225-18230) was fused with the green fluorescent protein gene eGFP and placed under the control of the CaMV 35S promoter, thereby constructing a 35S::OsMYB103L-eGFP expression vector. The recombinant vector and the control empty vector were respectively introduced into the inner epidermis of the onion by a gene gun-mediated method, and after 24 hours of culture, the eGFP fluorescence signal was observed under a laser confocal microscope. The green fluorescent...
Embodiment 3
[0060] Embodiment 3, the expression analysis of OsMYB103L gene
[0061] To study the expression pattern of the OsMYB103L gene, it was first analyzed by quantitative RT-PCR in the roots, stems, leaves, young panicles (less than 5 mm in length) and mature panicles of the indica rice variety Kasalath (Oryza sativa L. subsp. indica cv. Kasalath). expression in other tissues. The fluorescent signal (expressed in Ct value) of OsMYB103L gene and the fluorescent signal (expressed in Ct value) of Actin1 gene (internal reference gene) were calculated according to the formula (relative expression amount=2 -ΔCt , where ΔCt=Ct 目的基因 -Ct 内参基因 ) calculated value as the relative expression level of OsMYB103L gene, the results are shown in image 3 . The results showed that the OsMYB103L gene was expressed in roots, stems, leaves and mature ears, with the highest expression level in stems, relatively low expression levels in roots, leaves and mature ears, and basically no expression in youn...
PUM
Property | Measurement | Unit |
---|---|---|
Curvature | 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