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在杂交群体中进行 QTL 作图:成功与挑战。

QTL mapping in outbred populations: successes and challenges.

机构信息

Department of Pediatrics, Human and Molecular Genetics Center and Children's Research Institute, Medical College of Wisconsin, Milwaukee, Wisconsin.

出版信息

Physiol Genomics. 2014 Feb 1;46(3):81-90. doi: 10.1152/physiolgenomics.00127.2013. Epub 2013 Dec 10.

Abstract

Quantitative trait locus (QTL) mapping in animal populations has been a successful strategy for identifying genomic regions that play a role in complex diseases and traits. When conducted in an F2 intercross or backcross population, the resulting QTL is frequently large, often encompassing 30 Mb or more and containing hundreds of genes. To narrow the locus and identify candidate genes, additional strategies are needed. Congenic strains have proven useful but work less well when there are multiple tightly linked loci, frequently resulting in loss of phenotype. As an alternative, we discuss the use of highly recombinant outbred models for directly fine-mapping QTL to only a few megabases. We discuss the use of several currently available models such as the advanced intercross (AI), heterogeneous stocks (HS), the diversity outbred (DO), and commercially available outbred stocks (CO). Once a QTL has been fine-mapped, founder sequence and expression QTL mapping can be used to identify candidate genes. In this regard, the large number of alleles found in outbred stocks can be leveraged to identify causative genes and variants. We end this review by discussing some important statistical considerations when analyzing outbred populations. Fine-resolution mapping in outbred models, coupled with full genome sequence, has already led to the identification of several underlying causative genes for many complex traits and diseases. These resources will likely lead to additional successes in the coming years.

摘要

动物群体中的数量性状基因座(QTL)定位是一种识别与复杂疾病和性状相关的基因组区域的成功策略。当在 F2 杂交或回交群体中进行时,所得的 QTL 通常很大,常常包含 30Mb 或更多,并且包含数百个基因。为了缩小基因座并鉴定候选基因,需要额外的策略。同基因系已被证明是有用的,但在存在多个紧密连锁的基因座时效果较差,经常导致表型丧失。作为替代方法,我们讨论了使用高度重组的远交模型直接将 QTL 精细映射到只有几个兆碱基。我们讨论了几种当前可用的模型,例如高级杂交(AI)、异质品系(HS)、多样性远交(DO)和商业上可获得的远交品系(CO)。一旦 QTL 被精细映射,就可以使用原始序列和表达 QTL 映射来鉴定候选基因。在这方面,远交品系中发现的大量等位基因可以被利用来鉴定致病基因和变体。最后,我们讨论了在分析远交群体时的一些重要统计考虑因素。在远交模型中的精细分辨率映射,加上全基因组序列,已经导致了许多复杂性状和疾病的许多潜在致病基因的鉴定。这些资源在未来几年可能会有更多的成功。

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QTL mapping in outbred populations: successes and challenges.在杂交群体中进行 QTL 作图:成功与挑战。
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