SNP molecular marker relating to peach tree bleeding disease resistance
A technology of peach gummosis and molecular markers, which is applied in the direction of recombinant DNA technology, microbial measurement/inspection, DNA/RNA fragments, etc., to achieve the effects of improving breeding efficiency, high accuracy, and high degree of separation
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Publication Date
- 2017-05-10
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Abstract
Description
technical field
[0001] The invention belongs to the technical field of peach tree breeding, and in particular relates to a SNP molecular marker related to peach tree gummosis resistance. Background technique
[0002] Peach is a Rosaceae drupe fruit tree native to western my country, and it is also one of the most widely cultivated fruit trees in the world. Peach gummosis is one of the important factors affecting the healthy and orderly development of peach industry, which has caused serious harm to peach production in my country.
[0003] Peach tree gummosis is caused by the infection of the fungus Botryosphaeria dothidea, which mainly occurs on the trunk and side branches of the tree, and develops into fruiting branches and fruits when the disease is severe. In the early stage of the disease, light yellow transparent glue flows out of the lenticels, and after the glue is solidified, it gradually turns reddish brown, the diseased part is slightly swollen, the cortex and xyl...
Examples
Embodiment Construction
[0041] The present invention will be further described below in conjunction with specific examples.
[0042] Embodiment The acquisition of the closely linked SNP molecular markers of the QTL associated with peach tree gummosis resistance comprises the following steps:
[0043] 1) Build F 1 hybrid population
[0044] F 1 Finally, 80 hybrid offspring were obtained, and the offspring populations were segregated for gummosis traits.
[0045] 2) Genomic DNA extraction
[0046] Use the Qiagen DNeasy mini Kit kit to extract genomic DNA from 2 peach parents and 80 hybrid offspring, and follow the method provided in the kit, as follows:
[0047] ①Weigh 0.1g of frozen leaves, quickly grind them in liquid nitrogen, and place them in a 2ml sterilized centrifuge tube.
[0048] ② Add 400 μl AP1 buffer solution and 4 μl RNase A to the above centrifuge tube, vortex and mix well, bathe in 65°C water for 10 minutes, and mix up and down 2-3 times.
[0049] ③ Add 130 μl AP2 buffer solution to...