Stability-mediated epistasis constrains the evolution of an influenza protein

被引:247
作者
Gong, Lizhi Ian [1 ]
Suchard, Marc A. [2 ,3 ,4 ]
Bloom, Jesse D. [1 ,5 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
[2] Univ Calif Los Angeles, Dept Biomath, Los Angeles, CA USA
[3] Univ Calif Los Angeles, Dept Biostat, Los Angeles, CA USA
[4] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA USA
[5] Fred Hutchinson Canc Res Ctr, Computat Biol Program, Seattle, WA 98104 USA
来源
ELIFE | 2013年 / 2卷
基金
美国国家卫生研究院;
关键词
CYTOTOXIC-T-LYMPHOCYTE; A-VIRUS; LIMIT ESCAPE; RNA-BINDING; NUCLEOPROTEIN; EPITOPES; IDENTIFICATION; POPULATION; ADAPTATION; GENERATION;
D O I
10.7554/eLife.00631
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
John Maynard Smith compared protein evolution to the game where one word is converted into another a single letter at a time, with the constraint that all intermediates are words: WORD -> WORE -> GORE -> GONE -> GENE. In this analogy, epistasis constrains evolution, with some mutations tolerated only after the occurrence of others. To test whether epistasis similarly constrains actual protein evolution, we created all intermediates along a 39-mutation evolutionary trajectory of influenza nucleoprotein, and also introduced each mutation individually into the parent. Several mutations were deleterious to the parent despite becoming fixed during evolution without negative impact. These mutations were destabilizing, and were preceded or accompanied by stabilizing mutations that alleviated their adverse effects. The constrained mutations occurred at sites enriched in T-cell epitopes, suggesting they promote viral immune escape. Our results paint a coherent portrait of epistasis during nucleoprotein evolution, with stabilizing mutations permitting otherwise inaccessible destabilizing mutations which are sometimes of adaptive value.
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页数:19
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