Two SNP markers in close linkage with cucumber powdery mildew resistance and application thereof
A technology for powdery mildew resistance and powdery mildew resistance, applied in the fields of genetic engineering and molecular biology, can solve the problems of weak powdery mildew resistance gene mapping research and no SNP markers, and achieve the effect of accelerating the breeding process
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Embodiment 1
[0023] 1. Construction of genetic segregation populations and identification of exchanged individual plants
[0024] 1. F 2 Group construction
[0025] D8 (female parent), high susceptibility to powdery mildew inbred line; quoted from the University of North Carolina, USA, the stem is thick, and when the internode grows to 12-14 nodes, the top is capped with a bunch of female flowers and stops growing, the leaves are dark green, and the fruit is short , thick flesh, dark green peel; JIN5-508 (male parent), highly resistant to powdery mildew; it is a creeping strain with tall plants and long internodes, which is derived from the domestic variety "Jinchun 5" (Tianjin Kerun Agricultural Technology Co., Ltd. The company) continuously selfed and separated for 8 generations, selected plants with high resistance to powdery mildew in each offspring, and self-crossed to the 8th generation to obtain a high-resistant cucumber powdery mildew and long-fruited inbred line. This implementa...
Embodiment 2
[0049] (1) Select 8 cucumber lines known to be resistant to powdery mildew, 4 of which are resistant to powdery mildew (R210, EP112, GY114, JD65), and 4 are susceptible to powdery mildew (LL017, CJ223, EP56, SD41);
[0050] (2) Extract the above-mentioned eight strains and parental genomic DNA respectively, use the dCAPS markers derived from Chr6SNP-pm01 and Chr6SNP-pm02 to perform PCR amplification, and then use AluI restriction endonuclease to digest the amplified Chr6SNP-pm01 primer pair The PCR product, using DdeI restriction endonuclease to digest the PCR product amplified by the Chr6SNP-pm02 primer pair;
[0051] (3) The results of agarose gel electrophoresis showed that the identification of disease resistance was consistent with the results of double enzyme digestion ( Figure 7 , Figure 8 ), the above two SNP markers can distinguish powdery mildew resistant from susceptible powdery mildew strains.
[0052]
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