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Fine mapping and DNA fiber FISH analysis locates the tobamovirus resistance gene L3 of Capsicum chinense in a 400-kb region of R-like genes cluster embedded in highly repetitive sequences

机译:精细定位和DNA纤维FISH分析将辣椒的烟草花叶病毒抗性基因L3定位在嵌入高度重复序列的R样基因簇的400 kb区域中

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摘要

The tobamovirus resistance gene L3 of Capsicum chinense was mapped using an intra-specific F2 population (2,016 individuals) of Capsicum annuum cultivars, into one of which had been introduced the C. chinenseL3 gene, and an inter-specific F2 population (3,391 individuals) between C. chinense and Capsicum frutescence. Analysis of a BAC library with an AFLP marker closely linked to L3-resistance revealed the presence of homologs of the tomato disease resistance gene I2. Partial or full-length coding sequences were cloned by degenerate PCR from 35 different pepper I2 homologs and 17 genetic markers were generated in the inter-specific combination. The L3 gene was mapped between I2 homolog marker IH1-04 and BAC-end marker 189D23M, and located within a region encompassing two different BAC contigs consisting of four and one clones, respectively. DNA fiber FISH analysis revealed that these two contigs are separated from each other by about 30 kb. DNA fiber FISH results and Southern blotting of the BAC clones suggested that the L3 locus-containing region is rich in highly repetitive sequences. Southern blot analysis indicated that the two BAC contigs contain more than ten copies of the I2 homologs. In contrast to the inter-specific F2 population, no recombinant progeny were identified to have a crossover point within two BAC contigs consisting of seven and two clones in the intra-specific F2 population. Moreover, distribution of the crossover points differed between the two populations, suggesting linkage disequilibrium in the region containing the L locus.
机译:利用辣椒的种内F2种群(2,016个个体),对中国辣椒的烟草花叶病毒抗性基因L3进行定位,其中一个已引入了中华种C. chinenseL3基因和一个种间F2种群(3,391个个体)在C. chinense和辣椒的果实之间。用AFLP标记与L3抗性紧密相关的BAC库进行分析,结果表明存在番茄抗病基因I2的同源物。通过简并PCR从35种不同的胡椒I2同源物中克隆了部分或全长编码序列,并以种间组合产生了17种遗传标记。 L3基因被定位在I2同源标记IH1-04和BAC末端标记189D23M之间,并且位于包含分别由四个和一个克隆组成的两个不同的BAC重叠群的区域内。 DNA纤维FISH分析表明这两个重叠群彼此之间相距约30kb。 DNA纤维的FISH结果和BAC克隆的Southern印迹表明,含有L3基因座的区域富含高度重复的序列。 Southern印迹分析表明,两个BAC重叠群含有十个以上的I2同源物拷贝。与种间F2种群相反,在种内F2种群中,没有两个重组BAC重叠群中有7个和2个克隆的杂交后代。此外,在两个种群之间,交叉点的分布不同,这表明在包含L基因座的区域中连锁不平衡。

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