An Expanded View of Complex Traits: From Polygenic to Omnigenic

被引:1725
作者
Boyle, Evan A. [1 ]
Li, Yang I. [1 ]
Pritchard, Jonathan K. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[3] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
GENOME-WIDE ASSOCIATION; GENETIC-VARIATION; HUMAN ADAPTATION; HUMAN-DISEASES; HERITABILITY; RARE; SCHIZOPHRENIA; ARCHITECTURE; MUTATIONS; VARIANTS;
D O I
10.1016/j.cell.2017.05.038
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A central goal of genetics is to understand the links between genetic variation and disease. Intuitively, one might expect disease-causing variants to cluster into key pathways that drive disease etiology. But for complex traits, association signals tend to be spread across most of the genome-including near many genes without an obvious connection to disease. We propose that gene regulatory networks are sufficiently interconnected such that all genes expressed in disease-relevant cells are liable to affect the functions of core disease-related genes and that most heritability can be explained by effects on genes outside core pathways. We refer to this hypothesis as an "omnigenic" model.
引用
收藏
页码:1177 / 1186
页数:10
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