首页> 外文期刊>Czech Journal of Genetics and Plant Breeding >Identification of molecular markers associated with genic male sterility in tetraploid cotton ( Gossypium hirsutum L.) through bulk segregant analysis using a cotton SNP 63K array
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Identification of molecular markers associated with genic male sterility in tetraploid cotton ( Gossypium hirsutum L.) through bulk segregant analysis using a cotton SNP 63K array

机译:使用棉花SNP 63K阵列通过批量分离分析确定与四倍体棉(Gossypium hirsutum L.)中的雄性不育相关的分子标记

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Genic male sterility (GMS) is one of the most important economic traits for cotton ( Gossypium hirsutum L.) hybrid seed production. The GMS trait conferred by two recessive alleles ms5 and ms6 in homozygous constitution is widely used for cotton hybrid seed production in India. Identification of molecular markers closely linked to the ms5 and ms6 alleles would be useful in effective transferring in a short time male-sterility genes into cultivars or elite lines using marker-assisted backcrossing. Here, we describe a quick method to identify markers for GMS genes using bulk segregant analysis (BSA) in the interspecific ( G. hirsutum × G. hirsutum ) biparental population. The parents and bulks were genotyped with a cotton single nucleotide polymorphism?(SNP) 63K?array that contains 63 058 SNP markers including 45 104 intraspecific and 17 954 interspecific SNP?markers. Four SNP markers were found to be linked with the Ms5 and Ms6 genes. The markers i23493Gh and i46470Gh linked with the Ms5 gene, and other two markers i08605Gh and i08573Gh linked with the Ms6 gene are located on chromosome 12 and 26, respectively. A simple and cost effective tetra-primer amplification refractory mutation system PCR (tetra-primer ARMS-PCR) assay was optimized for screening a large number of breeding samples with the identified SNP markers in a short time. The molecular markers developed in this study will facilitate the marker-assisted selection (MAS) and accelerate the development of new GMS lines to use in cotton hybrid seed production.
机译:雄性不育(GMS)是棉花(Gossypium hirsutum L.)杂交种子生产的最重要经济性状之一。由纯合子组成的两个隐性等位基因ms5和ms6赋予的GMS性状被广泛用于印度的棉花杂交种子生产。鉴定与ms5和ms6等位基因紧密相关的分子标记,将有助于使用标记辅助回交技术在短时间内将雄性不育基因有效转移到品种或优良品系中。在这里,我们描述了一种在种间(G. hirsutum×G. hirsutum)双亲种群中使用本体分离分析(BSA)识别GMS基因标记的快速方法。用棉单核苷酸多态性(SNP)63Kα阵列对亲本和大块进行基因分型,该阵列包含63 058个SNP标记,包括45 104种种内和17 954种种间SNP标记。发现四个SNP标记与Ms5和Ms6基因相关。与Ms5基因连锁的标记i23493Gh和i46470Gh,与Ms6基因连锁的其他两个标记i08605Gh和i08573Gh分别位于12号和​​26号染色体上。优化了一种简单且经济高效的四引物扩增难治性突变系统PCR(四引物ARMS-PCR)检测方法,用于在短时间内筛选出具有鉴定出的SNP标记的大量育种样品。在这项研究中开发的分子标记将促进标记辅助选择(MAS),并加速开发用于棉花杂交种子生产的新GMS品系。

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