Epistasis and natural selection shape the mutational architecture of complex traits

被引:82
|
作者
Jones, Adam G. [1 ]
Buerger, Reinhard [2 ]
Arnold, Stevan J. [3 ]
机构
[1] Texas A&M Univ, Dept Biol, College Stn, TX 77843 USA
[2] Univ Vienna, Inst Math, A-1090 Vienna, Austria
[3] Oregon State Univ, Dept Integrat Biol, Corvallis, OR 97331 USA
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
基金
奥地利科学基金会; 美国国家科学基金会;
关键词
POPULATION GENETIC THEORY; DIFFERENTIAL EPISTASIS; STABILIZING SELECTION; MISSING HERITABILITY; G-MATRIX; EVOLUTION; EVOLVABILITY; ROBUSTNESS; POLYMORPHISM; COVARIANCE;
D O I
10.1038/ncomms4709
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The evolutionary trajectories of complex traits are constrained by levels of genetic variation as well as genetic correlations among traits. As the ultimate source of all genetic variation is mutation, the distribution of mutations entering populations profoundly affects standing variation and genetic correlations. Here we use an individual-based simulation model to investigate how natural selection and gene interactions (that is, epistasis) shape the evolution of mutational processes affecting complex traits. We find that the presence of epistasis allows natural selection to mould the distribution of mutations, such that mutational effects align with the selection surface. Consequently, novel mutations tend to be more compatible with the current forces of selection acting on the population. These results suggest that in many cases mutational effects should be seen as an outcome of natural selection rather than as an unbiased source of genetic variation that is independent of other evolutionary processes.
引用
收藏
页数:10
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