Molecule marker of characteristics of cotton yield or quality of fibre
A cotton fiber and molecular marker technology, which can be used in plant genetic improvement, botanical equipment and methods, applications, etc., and can solve problems such as low efficiency
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Embodiment 1
[0044] Extraction and Purification of Cotton Genomic DNA
[0045] Referring to the method reported by Song Guoli et al. (1998) with slight modifications, the basic steps are briefly described as follows:
[0046] (1) Cotton genomic DNA extraction:
[0047] Step 1: Add 2% β-mercaptoethanol to the extract, and preheat it in water at 65°C.
[0048] Step 2: Take out an appropriate amount of frozen leaves (about 2g) from the ultra-low temperature (-70°C) refrigerator, immediately put them into a pre-cooled mortar, add liquid nitrogen, quickly grind them into powder, and immediately put them into a container with a small amount of activated carbon. Add 0.6ml extract solution to a 1.5ml centrifuge tube, mix well, and bathe in water at 65°C for 60min. (Mix once every 10 minutes or so to fully disperse the sample).
[0049] The third step: after the water bath is completed, add an equal volume of chloroform-isoamyl alcohol (24:1, V / V), cover the lid, slowly invert the centrifuge tub...
Embodiment 2
[0062] Establishment of target traits pole plant bank
[0063] According to the BSA method proposed by Michelmore (1991), 5 F2 individual plants with extreme performance of each trait were selected from the population, and their DNA was mixed in equal amounts to construct the extreme value gene pool of each trait, with a final concentration of 10 ng / μl .
Embodiment 3
[0065] Tag screening
[0066] According to the performance of fiber traits in the F2 population, a mixed pool of extreme value DNA for six traits, including fiber strength, length, micronaire value, uniformity, coat percentage, and elongation, was constructed, and the parents were first screened with 386 pairs of SSR primers. The differential primers were then screened with the established extreme DNA pool, and the differential primers obtained from the extreme DNA pool were amplified and detected for all F2 single plants, and a total of 5 polymorphic markers were obtained.
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