A pair of special primers for assisted evaluation of relevant locus of soybean seed weight and method thereof
A 100-kernel weight and soybean technology, which is applied to a pair of special primers for assisting identification of soybean 100-kernel weight-related loci and the field thereof, can solve the problems of rarely found trait gene molecular markers and map positioning, etc., to improve breeding efficiency and Soybean Yield Level, Effects of Shortening Breeding Cycle
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Embodiment 1
[0022] Example 1. Acquisition of soybean 100-kernel weight-related locus (high 100-kernel weight-related locus) hsw3
[0023] 1. Primer synthesis
[0024] Satt126 primer pair sequence was obtained from the SOYBASE database; the upstream forward primer sequence was: 5'-GCTTGGTAGCTGTAGGAA-3'; the downstream reverse primer sequence was: 5'-ATAAAACAAATTCG CTGATAT-3', which was synthesized by Beijing Osaibo Biological Company.
[0025] 2. Parental genome amplification detection
[0026] The parents used to create soybean recombinant inbred line (recombinant inbred line, RIL) population were Zhonghuang 4 (National Soybean Germplasm Bank) and Zhongpin 661 (National Soybean Germplasm Bank). Zhonghuang 4 is the female parent, and its grain volume is relatively large (22.0-26.5 g / 100 grains); Zhongpin 661 is the male parent, and its grain volume is small (17.7-19.5 g / 100 grains).
[0027] Genomic DNA was extracted from parental leaves by CTAB method, and the amplification experiment w...
Embodiment 2
[0033] Example 2, Correlation verification between the amplified product of the Satt126 primer pair and the grain weight trait
[0034] 48 soybean resource materials (homozygous varieties or lines) were collected from different soybean ecological regions in my country.
[0035] The genomic DNA of each soybean plant leaf was extracted by CTAB method, and the PCR amplification experiment was carried out with Satt126 primer pair. The PCR reaction system is: 10×Buffer 2μl (containing Mg 2+ ), dNTP 0.4μl (10mM), upstream forward primer and downstream reverse primer 2μl (5μM), genomic DNA 1μl (40ng / μl), Taq enzyme 0.5μl (5U / μl), the reaction volume is 20μl, dropwise A drop of mineral oil to cover. The PCR reaction program was: 94°C for 5min; 35 cycles of 94°C for 60s, 53.5°C for 60s, and 72°C for 60s; 72°C for 10min.
[0036] PCR amplification products were analyzed by 9% polyacrylamide gel electrophoresis, stained by rapid silver staining and observed and photographed under ultr...
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