Rare allelic variation of wheat grain weight gene TaGW2-6A and molecular marker and application thereof
A gene and grain weight technology, applied in the biological field, can solve the problems of uncertain genetic effects of QTLs and inability to accurately select target QTLs.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0060] Embodiment 1, the acquisition of molecular markers related to wheat grain weight
[0061] 1. Alignment of CDS sequences of TaGW2-6A gene
[0062] Yumai 8679 (YM8679) and Jing 411 (J411) are commonly used wheat varieties, but there are differences in grain weight between them. Therefore, the TaGW2-6A gene related to grain weight in the genomes of Yumai 8679 (YM8679) and Jing 411 (J411) was cloned, and the differences between the two in different varieties were compared. The CDS sequence of the TaGW2-6A gene is completely identical, which is sequence 1 in the sequence listing, and the sequence length is 1278 bp, encoding a protein TaGW2-6A with 425 amino acids, and the amino acid sequence of the protein is sequence 2 in the sequence listing.
[0063] Align the amino acid sequence of the RING domain of TaGW2-6A protein with the RING domain of other species, the results are as follows figure 1 shown.
[0064] figure 1 In the figure, the horizontal line is the RING domai...
Embodiment 2
[0136] Embodiment 2, application of grain weight-related molecular markers
[0137] 1. Obtaining the samples to be tested
[0138] Using Yumai 8679 as the female parent and Jing 411 as the male parent, the hybrid offspring F was obtained by crossing 1 After that, the derived F 2 generational segregation groups.
[0139] 2. PCR amplification of molecular markers related to grain weight
[0140] Extract Yumai 8679, Jing 411 and F 2 Genomic DNA of each individual plant in the first-generation segregation population was used as a template, and the primers TaGW2-6Atgw primers in Example 1 were used for PCR amplification to obtain PCR amplification products.
[0141] Check the size of the PCR product.
[0142] f 2 The PCR amplification products of 41 individual plants in the generation isolation population only contained a fragment of 222bp (1705-1926 nucleotides in sequence 3), and the TaGW2-6A gene promoter of these wheats lacked a 114bp DNA fragment. Genotype is defined as...
PUM
| Property | Measurement | Unit |
|---|---|---|
| length | aaaaa | aaaaa |
| length | aaaaa | aaaaa |
| perimeter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


