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Development of SCAR markers linked to L-3 gene in capsicum

机译:与辣椒中L-3基因连锁的SCAR标记的开发

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摘要

Random amplified polymorphic DNA (RAPD) markers linked to the V locus were developed by applying the bulked segregant analysis method to two doubled haploid (DH) populations in Capsicum. The codominant RAPD markers, E18(272) and E18(286), were converted into sequence-characterized amplified region (SCAR) markers by molecular cloning and nucleotide sequencing. A PCR analysis using DH (n = 176) and backcross (n = 190) populations revealed that all the SCAR markers, PMFR11(269), PMFR11(283) and PMFR21(200), co-segregated with the original RAPD markers, and were mapped at a distance of 4.0 cM from the L-3 locus. Furthermore, after confirmation of their validity in 18 accessions of Capsicum spp. using the codominant SCAR marker pair, PMFR11269 and PMFR11283, it was suggested that the SCAR markers developed here could become effective in marker-assisted selection programs for the introduction of the L-3 gene derived from PI159236 (C. chinense) into sweet pepper for breeding purposes.
机译:通过对辣椒中的两个双倍单倍体(DH)群体应用大量的分离子分析方法,开发了与V基因座相关的随机扩增多态DNA(RAPD)标记。通过分子克隆和核苷酸测序将共性的RAPD标记物E18(272)和E18(286)转化为序列特征性扩增区(SCAR)标记物。使用DH(n = 176)和回交(n = 190)群体进行的PCR分析显示,所有SCAR标记PMFR11(269),PMFR11(283)和PMFR21(200)与原始RAPD标记共同分离,并且距离L-3基因座4.0 cM的基因被定位。此外,在确认其在辣椒属18种的有效性之后。使用共显性的SCAR标记对PMFR11269和PMFR11283,表明此处开发的SCAR标记可在标记辅助选择程序中有效,以将源自PI159236(C. chinense)的L-3基因引入甜椒中。育种目的。

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