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利用DNA-SSR标记对亲本未知的棉花杂交种进行品种纯度的分子鉴定。

Molecular identification of variety purity in a cotton hybrid with unknown parentage using DNA-SSR markers.

作者信息

Fu X Q, Yang F X, Lu X K, Wang X G, Yang B X, Liu F J, Liu Y, Peng J

机构信息

Institute of Cotton Research, Chinese Academy of Agricultural Sciences, State Key Laboratory of Cotton Biology, Key Laboratory for Cotton Genetic Improvement, Ministry of Agriculture, Anyang, , China.

, , China.

出版信息

Genet Mol Res. 2017 Sep 27;16(3):gmr-16-03-gmr.16039799. doi: 10.4238/gmr16039799.

DOI:10.4238/gmr16039799
PMID:28973776
Abstract

Molecular identification of hybrid purity is difficult in regional trials of cotton varieties and hybrid trials. In particular, the molecular detection of hybrid purity has not yet been reported in the case of unknown parentage. In this study, we screened 5000 pairs of primers and chose 17 pairs of core simple sequence repeat (SSR) primers to determine the F1 purity of Han6402. The results showed that the purity based on SSR markers reached 100%. Twelve of the 17 pairs of primers exhibited co-dominant banding patterns, and 5 showed non-co-dominant banding patterns. Moreover, we constructed an F1 SSR fingerprinting profile that enabled the identification of the authenticity of Han 6402. Using these primers, we subsequently detected 44 individual F2 seedlings, and the results exhibited different extents of separation, in which the majority of genotypes were heterozygous with co-dominance at most of the loci that differed from each other. The results validated the underlying heterozygous status of the F2 population at the molecular level. Therefore, we conclude that the set of core SSR primers can be used for the laboratory identification of the authenticity and purity of cotton hybrids, not only for distinguishing Fl hybrids or segregating F2 populations, but also for detecting volunteer seeds as fake F1 hybrids in the cotton hybrid industry, based on the hybrid fingerprinting.

摘要

在棉花品种区域试验和杂交试验中,杂交种纯度的分子鉴定较为困难。特别是在亲本未知的情况下,尚未见杂交种纯度的分子检测报道。本研究筛选了5000对引物,选取17对核心简单序列重复(SSR)引物来测定邯6402的F1纯度。结果表明,基于SSR标记的纯度达到100%。17对引物中有12对呈现共显性带型,5对呈现非共显性带型。此外,我们构建了一个F1 SSR指纹图谱,可用于鉴定邯6402的真实性。利用这些引物,我们随后检测了44株F2单株幼苗,结果显示出不同程度的分离,其中大多数基因型在大多数相互不同的位点上是杂合且共显性的。结果在分子水平上验证了F2群体潜在的杂合状态。因此,我们得出结论,这套核心SSR引物可用于实验室鉴定棉花杂交种的真实性和纯度,不仅可用于区分F1杂交种或分离的F2群体,还可基于杂交指纹图谱检测棉花杂交行业中作为假F1杂交种的自生苗。

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