SNP Molecular Marker, Detection Method and Application of Wheat Leaf Rust Resistance Gene lr42
An anti-leaf rust gene and molecular marker technology, applied in biochemical equipment and methods, microbial determination/inspection, recombinant DNA technology, etc., can solve the problems of inability to meet the needs of modern breeding, complex detection procedures, poor accuracy, etc. Achieve the effect of easy automation, high detection throughput and high accuracy
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Embodiment 1
[0036] The method for obtaining the SNP molecular marker TC113325 of wheat leaf rust resistance gene Lr42 comprises the following steps:
[0037] (1) Construction of high-generation genetic segregation population:
[0038] Using the existing molecular markers of Lr42: Xcfd15 and Xwmc432 to scan the F4 generation population of KS93U50 / Morocco, it was found that the genetically isolated individual plants were heterozygous genotypes at the disease resistance site. Planted as high generation genetic segregants;
[0039] (2) Obtain SNP molecular markers and design amplification primers:
[0040] Using the homologous segment sequences of the wheat chromosome segments of the existing molecular markers Xcfd15 and Xwmc432 of Lr42 in closely related species such as rice, Brachypodium, and barley, to find genes with disease resistance domains, and use the found genes to Primers were designed for its conserved domain, and after verification by the KS93U50 / Morocco high-generation segrega...
Embodiment 2
[0042] The detection method of wheat leaf rust resistance gene Lr42 comprises the following steps:
[0043] (1) Take 93 seeds of an isolated F5 population of KS93U50 / Morocco and plant them in the greenhouse. When the population grows to three leaves and one heart, extract population DNA: use QIAGEN's DNeasy Plant MiniKit to extract according to the instructions; all populations After the sample DNA is extracted, perform DNA integrity electrophoresis detection, and use a concentration meter to measure the sample DNA concentration, and dilute all sample concentrations to 50-100ng / ul according to the measurement results;
[0044] (2) PCR amplification of molecular markers: PCR amplification system is: DNA 2.5ul (50-100ng / ul); mixed primer 0.07ul (SEQ ID NO.1:SEQ ID NO.1:SEQ ID NO.1: H2O=12:12:30:46); MasterMix 3ul (2×); ddH2O 0.493ul; PCR reaction total volume 6.0ul;
[0045] The PCR amplification program was as follows: denaturation at 94°C for 15 min; denaturation at 95°C for ...
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