A Systematic Survey of an Intragenic Epistatic Landscape

被引:93
作者
Bank, Claudia [1 ,2 ]
Hietpas, Ryan T. [3 ]
Jensen, Jeffrey D. [1 ,2 ]
Bolon, Daniel N. A. [3 ]
机构
[1] Ecole Polytech Fed Lausanne, Sch Life Sci, CH-1015 Lausanne, Switzerland
[2] SIB, Lausanne, Switzerland
[3] Univ Massachusetts, Sch Med, Dept Biochem & Mol Pharmacol, Worcester, MA USA
基金
瑞士国家科学基金会; 美国国家卫生研究院; 欧洲研究理事会;
关键词
epistasis; experimental evolution; fitness landscapes; distribution of fitness effects; DOUBLE-MUTANT CYCLES; PROTEIN-PROTEIN INTERACTIONS; MUTATIONAL ROBUSTNESS; BENEFICIAL MUTATIONS; FITNESS LANDSCAPES; CRYSTAL-STRUCTURE; HSP90; CHAPERONE; RNA VIRUS; EVOLUTION; STABILITY;
D O I
10.1093/molbev/msu301
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
Mutations are the source of evolutionary variation. The interactions of multiple mutations can have important effects on fitness and evolutionary trajectories. We have recently described the distribution of fitness effects of all single mutations for a nine-amino-acid region of yeast Hsp90 (Hsp82) implicated in substrate binding. Here, we report and discuss the distribution of intragenic epistatic effects within this region in seven Hsp90 point mutant backgrounds of neutral to slightly deleterious effect, resulting in an analysis of more than 1,000 double mutants. We find negative epistasis between substitutions to be common, and positive epistasis to be rare-resulting in a pattern that indicates a drastic change in the distribution of fitness effects one step away from the wild type. This can be well explained by a concave relationship between phenotype and genotype (i.e., a concave shape of the local fitness landscape), suggesting mutational robustness intrinsic to the local sequence space. Structural analyses indicate that, in this region, epistatic effects are most pronounced when a solvent-inaccessible position is involved in the interaction. In contrast, all 18 observations of positive epistasis involved at least one mutation at a solvent-exposed position. By combining the analysis of evolutionary and biophysical properties of an epistatic landscape, these results contribute to a more detailed understanding of the complexity of protein evolution.
引用
收藏
页码:229 / 238
页数:10
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