Literature DB >> 30039542

Estimating the contribution of folding stability to nonspecific epistasis in protein evolution.

Pouria Dasmeh1,2,3, Adrian W R Serohijos1,2.   

Abstract

The extent of nonadditive interaction among mutations or epistasis reflects the ruggedness of the fitness landscape, the mapping of genotype to reproductive fitness. In protein evolution, there is strong support for the importance and prevalence of epistasis but the quantitative and relative contribution of various factors to epistasis are poorly known. Here, we determine the contribution of selection for folding stability to epistasis in protein evolution. By combining theoretical estimates of the rates of molecular evolution and the nonlinear mapping between protein folding thermodynamics and fitness, we show that the simple selection for folding stability imposes at least ~30% to ~40% epistasis in long-term protein evolution. Estimating the contribution of governing factors in molecular evolution such as protein folding stability to epistasis will provide a better understanding of epistasis that could improve methods in molecular evolution.
© 2018 Wiley Periodicals, Inc.

Keywords:  epistasis; fitness landscape; protein evolution; protein fitness; protein stability

Mesh:

Substances:

Year:  2018        PMID: 30039542     DOI: 10.1002/prot.25588

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  4 in total

1.  Pervasive Pairwise Intragenic Epistasis among Sequential Mutations in TEM-1 β-Lactamase.

Authors:  Courtney E Gonzalez; Marc Ostermeier
Journal:  J Mol Biol       Date:  2019-03-25       Impact factor: 5.469

2.  Low protein expression enhances phenotypic evolvability by intensifying selection on folding stability.

Authors:  Shraddha Karve; Pouria Dasmeh; Jia Zheng; Andreas Wagner
Journal:  Nat Ecol Evol       Date:  2022-07-07       Impact factor: 19.100

3.  Highly expressed genes evolve under strong epistasis from a proteome-wide scan in E. coli.

Authors:  Pouria Dasmeh; Éric Girard; Adrian W R Serohijos
Journal:  Sci Rep       Date:  2017-11-20       Impact factor: 4.379

4.  Characterizing Amino Acid Substitution with Complete Linkage of Sites on a Lineage.

Authors:  Tristan L Stark; David A Liberles
Journal:  Genome Biol Evol       Date:  2021-10-01       Impact factor: 3.416

  4 in total

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