Identifying recent adaptations in large-scale genomic data.

Identifying recent adaptations in large-scale genomic data.
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DOI:
10.1016/j.cell.2013.01.035
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发表时间:
2013-02-14
期刊:
影响因子:
64.5
通讯作者:
Sabeti PC
Sabeti PC
中科院分区:
生物学1区
文献类型:
--
作者:
Grossman SR;Andersen KG;Shlyakhter I;Tabrizi S;Winnicki S;Yen A;Park DJ;Griesemer D;Karlsson EK;Wong SH;Cabili M;Adegbola RA;Bamezai RN;Hill AV;Vannberg FO;Rinn JL;1000 Genomes Project;Lander ES;Schaffner SF;Sabeti PC

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While several hundred regions of the human genome harbor signals of positive natural selection, few of the relevant adaptive traits and variants have been elucidated. Using full-genome sequence variation from the 1000 Genomes Project (1000G) and the Composite of Multiple Signals (CMS) test, we investigated 412 candidate signals and leveraged functional annotation, protein structure modeling, epigenetics, and association studies to identify and extensively annotate candidate causal variants. The resulting catalog provides a tractable list for experimental follow-up; it includes thirty-five high-scoring non-synonymous variants, fifty-nine variants associated with expression levels of a nearby coding gene or lincRNA, and numerous variants associated with susceptibility to infectious disease and other phenotypes. We experimentally characterized one candidate non-synonymous variant in TLR5, and show that it leads to altered NF-κB signaling in response to bacterial flagellin.
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