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A bioinformatic and transcriptomic approach to identifying positional candidate genes without fine mapping: an example using rice root-growth QTLs.

机译:一种无需精细定位即可鉴定位置候选基因的生物信息学和转录组学方法:使用水稻根系生长QTL的示例。

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摘要

Fine mapping can accurately identify positional candidate genes for quantitative trait loci (QTLs) but can be time consuming, costly, and, for small-effect QTLs with low heritability, difficult in practice. We propose an alternative approach, which uses meta-analysis of original mapping data to produce a relatively small confidence interval for target QTLs, lists the underlying positional candidates, and then eliminates them using whole-genome transcriptomics. Finally, sequencing is conducted on the remaining candidate genes allowing identification of allelic variation in either expression or protein sequence. We demonstrate the approach using root-growth QTLs on chromosomes 2, 5, and 9 of the Bala x Azucena rice mapping population. Confidence intervals of 10.5, 9.6, and 5.4 cM containing 189, 322, and 81 genes, respectively, were produced. Transcriptomics eliminated 40% of candidate genes and identified nine expression polymorphisms. Sequencing of 30 genes revealed that 57% of the predicted proteins were polymorphic. The limitations of this approach are discussed.
机译:精细作图可以准确地为数量性状基因座(QTL)识别位置候选基因,但可能很耗时,成本高,并且对于遗传力低的小效应QTL来说,很难实现。我们提出了一种替代方法,该方法使用原始映射数据的荟萃分析为目标QTL产生相对较小的置信区间,列出潜在的位置候选物,然后使用全基因组转录组学消除它们。最后,对剩余的候选基因进行测序,从而鉴定出表达或蛋白质序列中的等位基因变异。我们证明了在Bala x Azucena水稻作图种群的2号,5号和9号染色体上使用根生长QTL的方法。分别产生10.5、9.6和5.4 cM的置信区间,分别包含189、322和81个基因。转录组学消除了40%的候选基因,并鉴定出9个表达多态性。对30个基因进行测序后发现,预测的蛋白质中有57%是多态性的。讨论了这种方法的局限性。

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