Method for building genetic map of bamboo plants
A genetic map and technology of bamboo plants, which are applied in the field of rapid construction of bamboo genetic map based on segregated populations of self-inbred generation, and rapid construction of high-density genetic linkage map of bamboo plants, can solve the problem of restricting bamboo plants and difficult to obtain bamboo plants. problems such as genetic maps, to achieve the effect of reducing the cost and time of genotyping, avoiding the contamination of progeny materials, and simplifying the construction process
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Embodiment 1
[0054] The construction of the self-bred genetic population of Mazhu:
[0055] The present embodiment selects the Ma bamboo (Dendrocalamus latiflorus Munro) that is widely distributed in the provinces of southern China as the experimental material, and the construction of the Ma bamboo genetic mapping population includes the following steps:
[0056] The 1st step, the collection of Ma bamboo parent plant:
[0057] Ma bamboo is a kind of clump bamboo. Several bamboo poles growing in a clump are propagated from one mother plant. We found a clump of Bamboo japonica in the early flowering stage in Mile City, Yunnan Province, and transplanted it to the greenhouse area of Kunming Institute of Botany, Chinese Academy of Sciences as a standby parent.
[0058] 2nd step, the selfing of bamboo parent plant:
[0059] First, use scissors to cut off the pollinated seeds and the exposed pistils (pollination status is unknown), and only keep the stamens and unreleased pistils; then, colle...
Embodiment 2
[0063] Constructing the genetic map of Mazhu:
[0064] Step 1, extraction of parental and offspring genomic DNA:
[0065] Randomly select 188 progeny individuals from the S1 population obtained in Example 1 for the construction of the genetic map of bamboo. Using the modified CTAB method to extract the whole genome DNA of the young leaves of the parents and offspring of Mazhu:
[0066] (1) Take 200ml 2% CTAB and preheat at 60°C, add 2‰ dithiothreitol and mix well,
[0067] (2) Weigh 80 mg of fresh young leaves, add liquid nitrogen and quickly grind them into powder, transfer to a 2ml small centrifuge tube filled with 1ml 60°C CTAB buffer solution, oscillate and mix well, 60°C water bath, 50min, during the mixing Second-rate,
[0068] (3) Take out the centrifuge tube and cool it for 2 minutes, add 1ml of chloroform-isoamyl alcohol with a volume ratio of 24:1, invert it upside down to mix well, and then centrifuge at 10,000rpm for 5 minutes at room temperature.
[0069] (4) ...
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