Linked KASP molecular markers for high temperature tolerance traits of rice and applications thereof
A technology of molecular markers and high temperature resistance, which is applied in the field of linked KASP molecular markers for high temperature resistance traits of rice, can solve the problems of high cost, achieve low cost, improve the efficiency of variety breeding, and promote the effect of genetic improvement
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Embodiment 1
[0048] The primer development and preparation method of molecular markers 7238, 6400, 7334, the steps are:
[0049] According to the inventor's previous research, a new set of chromosome segment substitution lines (CSSLs) was established using the high temperature tolerant indica rice variety N22 and the high temperature sensitive indica rice variety 9311, and their genetic basis was analyzed. The effects of high temperature stress on rice seedling and heading stages were studied using relative electrical conductivity (REC) and seed setting rate (SSR). This study clarified that the high temperature tolerance of rice at the heading stage has a significant positive correlation with its seed setting rate under high temperature stress. And the study identified five QTLs for high temperature resistance: qSSR6-1, qSSR7-1, qSSR8-1, qSSR9-1 and qSSR11-1. Among them, qSSR7-1 and qSSR11-1 explained higher phenotypic variation, which were 26.35% and 14.21%, respectively. For the two QT...
Embodiment 2
[0068] The primer application method of KASP molecular marker 7238,6400,7334, its steps are:
[0069] (1) Using the KASP molecular markers 7238, 6400, 7334 and genotyping methods provided by the summary of the invention, 10 individual plants of the 9311 / N22 CSSLs population were genotyped, and QTLqSSR7-1 and QTLqSSR11 with high temperature resistance were screened out Lines CSSL74, CSSL105 of -1 genome segment. CSSL74 carried the high temperature resistant QTLqSSR7-1, and CSSL105 carried the high temperature resistant QTLqSSR11-1.
[0070] (2) The two individual plants obtained in step (1) are crossed to obtain F 1 Seeds, planted in the field to get F 1 Generation single plant, each F 1 F 2 generation seeds.
[0071] (3) The F obtained in step (2) 2 Generation seeds were germinated in the laboratory, DNA was extracted, and 1200 strains of F 2 Genotype identification was carried out on the seedlings, and 52 homozygous individual plants that aggregated QTL qSSR7-1 and QTL...
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