GSBS Student Publications

Title

A systematic survey of an intragenic epistatic landscape

Student Author(s)

Ryan T. Hietpas

GSBS Program

Biochemistry & Molecular Pharmacology

UMMS Affiliation

Department of Biochemistry and Molecular Pharmacology

Date

1-1-2015

Document Type

Article

Medical Subject Headings

Amino Acid Substitution; Binding Sites; Computational Biology; *Epistasis, Genetic; *Evolution, Molecular; Genetic Fitness; Genotype; HSP90 Heat-Shock Proteins; Phenotype; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Solvents

Disciplines

Ecology and Evolutionary Biology | Genomics | Molecular Biology

Abstract

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.

Rights and Permissions

Citation: Mol Biol Evol. 2015 Jan;32(1):229-38. doi: 10.1093/molbev/msu301. Epub 2014 Nov 3. Link to article on publisher's site

DOI of Published Version

10.1093/molbev/msu301

Related Resources

Link to Article in PubMed

Journal Title

Molecular biology and evolution

PubMed ID

25371431