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本文引用的文献

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A map of human genome variation from population-scale sequencing.人类基因组变异的图谱来自于基于人群的测序。
Nature. 2010 Oct 28;467(7319):1061-73. doi: 10.1038/nature09534.
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Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants.200 个人类外显子组重测序发现低频非同义编码变异过度。
Nat Genet. 2010 Nov;42(11):969-72. doi: 10.1038/ng.680. Epub 2010 Oct 3.
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Identification of the bovine Arachnomelia mutation by massively parallel sequencing implicates sulfite oxidase (SUOX) in bone development.通过大规模平行测序鉴定出牛 Arachnomelia 突变,提示磺基氧化酶 (SUOX) 在骨骼发育中的作用。
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Genome-wide analysis of a long-term evolution experiment with Drosophila.对果蝇进行的一项长期进化实验的全基因组分析。
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Adaptation - not by sweeps alone.适应——不仅仅是横扫。
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Whole-genome resequencing reveals loci under selection during chicken domestication.全基因组重测序揭示了鸡驯化过程中的选择位点。
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Exome sequencing identifies the cause of a mendelian disorder.外显子组测序确定了一种孟德尔疾病的病因。
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Targeted capture and massively parallel sequencing of 12 human exomes.12个人类外显子组的靶向捕获和大规模平行测序
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靶向重测序影响温顺和攻击性的基因组区域揭示了多个正选择信号。

Targeted resequencing of a genomic region influencing tameness and aggression reveals multiple signals of positive selection.

机构信息

Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany.

出版信息

Heredity (Edinb). 2011 Sep;107(3):205-14. doi: 10.1038/hdy.2011.4. Epub 2011 Feb 9.

DOI:10.1038/hdy.2011.4
PMID:21304545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3183948/
Abstract

The identification of the causative genetic variants in quantitative trait loci (QTL) influencing phenotypic traits is challenging, especially in crosses between outbred strains. We have previously identified several QTL influencing tameness and aggression in a cross between two lines of wild-derived, outbred rats (Rattus norvegicus) selected for their behavior towards humans. Here, we use targeted sequence capture and massively parallel sequencing of all genes in the strongest QTL in the founder animals of the cross. We identify many novel sequence variants, several of which are potentially functionally relevant. The QTL contains several regions where either the tame or the aggressive founders contain no sequence variation, and two regions where alternative haplotypes are fixed between the founders. A re-analysis of the QTL signal showed that the causative site is likely to be fixed among the tame founder animals, but that several causative alleles may segregate among the aggressive founder animals. Using a formal test for the detection of positive selection, we find 10 putative positively selected regions, some of which are close to genes known to influence behavior. Together, these results show that the QTL is probably not caused by a single selected site, but may instead represent the joint effects of several sites that were targets of polygenic selection.

摘要

确定影响表型特征的数量性状基因座(QTL)中的致病遗传变异是具有挑战性的,特别是在外群品系之间的杂交中。我们之前已经在两个经人类行为选择的野生衍生的外群大鼠(Rattus norvegicus)品系之间的杂交中确定了几个影响温顺性和攻击性的 QTL。在这里,我们使用靶向序列捕获和对杂交起始动物中最强 QTL 中的所有基因进行大规模平行测序。我们确定了许多新的序列变异,其中有几个可能具有功能相关性。该 QTL 包含几个区域,其中温顺或攻击性起始动物都没有序列变异,而两个区域在起始动物之间存在替代性单倍型固定。对 QTL 信号的重新分析表明,致病位点可能在温顺起始动物中固定,但几个致病等位基因可能在攻击性起始动物中分离。使用用于检测正选择的正式测试,我们发现了 10 个可能的正选择区域,其中一些区域靠近已知影响行为的基因。总之,这些结果表明,该 QTL 可能不是由单个选择位点引起的,而是可能代表了多个被多基因选择的位点的联合效应。