Proceedings of the National Academy of Sciences · 2018 · 133 citations · 42 references
Life SciencesEvolutionary BiologyMolecular BiologyGenome EvolutionMicroevolutionMolecular EvolutionAncestral Sequence ReconstructionEpistasisEvolutionNatural SelectionProtein EvolutionSequence EvolutionAncestral Protein ReconstructionEpistasis In Protein EvolutionEvolutionary TrajectoriesMolecular Evolutionary ModelsProtein Ancestral ReconstructionProtein Evolution ModelsProtein Sequence EvolutionSubstitutions
Significance When mutations within a protein change each other’s functional effects—a phenomenon called epistasis—the paths available to evolution at any moment in time depend on the specific set of changes that previously occurred in the protein. The extent to which epistasis has shaped historical evolutionary trajectories is unknown. Using a high-precision bulk fitness assay and ancestral protein reconstruction, we measured the fitness effects in ancestral and extant sequences of all historical substitutions that occurred during the billion-year trajectory of an essential protein. We found that most historical substitutions were contingent on prior epistatic substitutions and/or entrenched by subsequent changes. These results establish that epistasis caused widespread, consequential shifts in the site-specific fitness constraints that shaped the protein’s historical trajectory.
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The Revised Classification of Eukaryotes
Sina M. Adl, Alastair G. B. Simpson, Christopher E. Lane et al. · Journal of Eukaryotic Microbiology · 2012 · 1.7K citations · Full text
Crystal structure of an Hsp90–nucleotide–p23/Sba1 closed chaperone complex
Maruf M. U. Ali, S. Mark Roe, Cara K. Vaughan et al. · Nature · 2006 · 977 citations · Full text
A new method of inference of ancestral nucleotide and amino acid sequences.
Zefeng Yang, Sudhir Kumar, M Nei · Genetics · 1995 · 754 citations · Full text