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首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >A high-resolution linkage map of the Rfd1, a restorer-of-fertility locus for cytoplasmic male sterility in radish (Raphanus sativus L.) produced by a combination of bulked segregant analysis and RNA-Seq
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A high-resolution linkage map of the Rfd1, a restorer-of-fertility locus for cytoplasmic male sterility in radish (Raphanus sativus L.) produced by a combination of bulked segregant analysis and RNA-Seq

机译:Rfd1的高分辨率连锁图谱,该图是通过大量分离剂分析和RNA-Seq结合产生的萝卜(Raphanus sativus L.)细胞质雄性不育的恢复力位点

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摘要

We utilized a combination of BSA and RNA-Seq to identify SNPs linked to the Rfd1 locus, a restorer-of-fertility gene in radish. A high-density linkage map was constructed using this approach. Male fertility of cytoplasmic male sterility conditioned by the Dongbu cytoplasmic and genic male-sterility cytoplasm can be restored by a restorer-of-fertility locus, Rfd1, in radish. To construct a high-density linkage map and to identify a candidate gene for the Rfd1 locus, bulked segregant analysis and RNA-seq approaches were combined. A total of 26 and 28 million reads produced from male-fertile and male-sterile bulked RNA were mapped to the radish reference unigenes. After stringent screening of SNPs, 327 reliable SNPs of 109 unigenes were selected. Arabidopsis homologs for 101 of the 109 genes were clustered around the 4,000 kb region of Arabidopsis chromosome 3, which was syntenic to the Rfd1 flanking region. Since the reference unigene set was incomplete, the contigs were de novo assembled to identify 134 contigs harboring SNPs. Most of SNP-containing contigs were also clustered on the same syntenic region in Arabidopsis chromosome. A total of 21 molecular markers positioned within a 2.1 cM interval including the Rfd1 locus were developed, based on the selected unigenes and contigs. A segregating population consisting of 10,459 individuals was analyzed to identify recombinants containing crossovers within this interval. A total of 284 identified recombinants were then used to construct a high-density map, which delimited the Rfd1 locus into an 83-kb syntenic interval of Arabidopsis chromosome 3. Since no candidate gene, such as a pentatricopeptide repeat (PPR)-coding gene, was found in this interval, 231 unigenes and 491 contigs containing putative PPR motifs were analyzed further, but no PPR gene in linkage disequilibrium with the Rfd1 locus could be found
机译:我们利用BSA和RNA-Seq的组合来鉴定与Rfd1基因座(萝卜中的生育力恢复基因)相关的SNP。使用此方法构建了一个高密度链接图。由冬补细胞质和基因雄性不育细胞质调节的细胞质雄性不育的雄性可通过萝卜的育性恢复位点Rfd1恢复。为了构建高密度连锁图谱并鉴定Rfd1基因座的候选基因,将大量的分离子分析法和RNA-seq方法结合起来。将从雄性可育和雄性不育大体积RNA产生的总共26和2,800万条读物中定位到萝卜参考单基因。在对SNP进行严格筛选后,选择了109个单基因的327个可靠SNP。 109个基因中101个的拟南芥同源物聚集在拟南芥3号染色体的4,000 kb区域周围,该区域与Rfd1侧翼区域同系。由于参考单基因集不完整,因此重新构建了重叠群,以鉴定出134个带有SNP的重叠群。多数含有SNP的重叠群也都聚集在拟南芥染色体的同一突触区域上。基于所选的单基因和重叠群,共开发了21个位于2.1 cM区间内的分子标记,包括Rfd1基因座。分析了由10,459个个体组成的隔离种群,以鉴定在此间隔内包含交叉的重组体。然后总共使用284个已鉴定的重组体来构建高密度图谱,该图谱将Rfd1基因座划入拟南芥3号染色体的83kb同音区间。由于没有候选基因,例如五肽重复序列(PPR)编码基因在此间隔中发现了231个具有推定PPR基序的单基因和491个重叠群,但未发现与Rfd1基因座连锁不平衡的PPR基因。

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