SSR (simple sequence repeat) markers on No.3 chromosome, closely linked to RBSDV (rice black-streaked dwarf virus) resistant QTL (quantitative trait locus) and application thereof
A rice black streak dwarfing and resistance technology, which is applied in the detection/testing of microorganisms, DNA/RNA fragments, recombinant DNA technology, etc., can solve problems such as interference, complex genetic mechanism, and influence on the reproducibility of results, and achieve accelerated breeding process, simplified selection methods, and improved breeding efficiency
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Embodiment 1
[0019] Example 1, Acquisition of Molecular Markers Tightly Linked to Major QTL for Rice Black-streaked Dwarf Resistance
[0020] 1. Plant material
[0021] In 2008, the parents Huaidao 5 and Tetebo were planted in the field of Jiangsu Academy of Agricultural Sciences, and hybrid F 1 , next year F 1 F 2 Seeds, propagated F in Hainan in 2009 2 group, as a mapping group. f 2 Individual plant number, parent and hybrid F at tillering stage 1 and F 2 Some leaves of each individual plant in the population were stored in a -70°C refrigerator for SSR analysis, F 2 Harvest the individual plants of the population for phenotypic identification. In 2010, the main susceptible cultivar Huaidao 5 and the resistant cultivars Tetebo and F 1 and F 2:3 The family was identified by artificial inoculation (Journal of Plant Protection, 2011, 38(4): 301-305).
[0022] 2. Screening of toxin-transmitting mediators
[0023] Collect rice diseased plants showing RBSDV symptoms (Zhejiang Agricu...
Embodiment 2
[0061] Example 2, the application of the molecular markers closely linked to the rice black-streaked dwarf resistance QTL on chromosome 3 in the offspring of the hybrid combination with Huaidao 5 and Tetebo as parents
[0062] The SSR marker closely linked to the rice black-streaked dwarf resistance QTL obtained on chromosome 3, the F 2:3 Part of the individual plants in the family were predicted for resistance to rice black-streaked dwarf disease, the DNA of each individual plant was extracted, and then PCR amplification analysis was performed with the primers of SSR markers RM5626 and RM7097, and the band type analysis was used to determine whether there were corresponding markers , the presence of the marker indicates that the line has reached the level of resistance to black-streaked dwarf disease, and the absence of the marker indicates that the line is susceptible to the disease. Then, the actual resistance to black-streaked dwarf disease of the tested lines was measured...
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