Molecular marker tightly linked with major QTL (Quantitative Trait Loci) of cotton seed oil content of upland cotton and application thereof
A technology of oil content and molecular markers, which is applied in the fields of cotton breeding and molecular biology, to improve breeding efficiency, reduce workload, and speed up selection progress
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Embodiment 1
[0023] Molecular markers closely linked to the main QTL for cottonseed oil content in upland cotton were obtained by the following methods:
[0024] (1) Construction of population and determination of cottonseed oil content:
[0025] The high-oil upland cotton variety DPLSR3 was used as the female parent, and the low-oil upland cotton variety Yancheng 115 was used as the male parent. In 2008, a hybrid combination was established at the Lishui Plant Experimental Base of the Jiangsu Academy of Agricultural Sciences. At the end of the same year, Hainan Nanfan F 1 , selfing produces F 2 . In 2009, F 2 and parents, a total of 151 F 2 Single plant, harvested F 2 Seed, to F 2 The seeds were fluffed and dried, and F was measured by near-infrared analysis method (Xu Peng, et al. 2 oil content. 2010 Planting F 2∶3 Plant rows, harvest seeds according to plant rows, also develvet and dry the seeds, and measure F by near-infrared analysis method 2∶3 oil content.
[0026] (2) Gene...
Embodiment 2
[0029] Molecular markers closely linked to the main QTL for cottonseed oil content in upland cotton were verified in genetic populations:
[0030] The cottonseed oil content of the derivative lines of upland cotton variety DPLSR3 was screened by molecular marker TMB1216 with a size of 190bp:
[0031] Identification object:
[0032] The upland cotton variety DPLSR3 was crossed with Yancheng 115 and propagated to F 3 Generation, they are used as the identification object of cottonseed oil content.
[0033] Identification process
[0034] a) Identification by molecular markers closely linked to the major QTL for cottonseed oil content in upland cotton
[0035] Firstly, the DNA obtained by separating and extracting the leaves of each identification object by CTAB extraction method, and then using the primers 5'AATTTAGTTTCATACACAC3'(SEQ ID NO:1) and 5'TGGTCACCCATCGTTAAC3'(SEQ ID NO:2) of the molecular marker TMB1216 to target These DNAs were subjected to polymerase chain reacti...
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