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dc.contributor.authorBank, Claudia
dc.contributor.authorHietpas, Ryan T.
dc.contributor.authorJensen, Jeffrey D.
dc.contributor.authorBolon, Daniel N.
dc.date2022-08-11T08:08:23.000
dc.date.accessioned2022-08-23T15:53:21Z
dc.date.available2022-08-23T15:53:21Z
dc.date.issued2014-10-23
dc.date.submitted2018-06-21
dc.identifier.citation<p>bioRxiv 010645; doi: https://doi.org/10.1101/010645. <a href="https://doi.org/10.1101/010645" target="_blank">Link to preprint on bioRxiv service.</a></p>
dc.identifier.doi10.1101/010645
dc.identifier.urihttp://hdl.handle.net/20.500.14038/29337
dc.description.abstractMutations 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 1000 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.
dc.language.isoen_US
dc.relation<p>Now published in <em>Molecular Biology and Evolution</em> doi: <a href="http://dx.doi.org/10.1093/molbev/msu301" target="_blank">10.1093/molbev/msu301</a>.</p>
dc.rightsThe copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC-ND 4.0 International license.
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectevolutionary biology
dc.subjectmutations
dc.subjectevolution
dc.subjectyeast Hsp90
dc.subjectintragenic epistatic effects
dc.subjectdouble-mutants
dc.subjectAmino Acids, Peptides, and Proteins
dc.subjectBiophysics
dc.subjectEcology and Evolutionary Biology
dc.subjectFungi
dc.subjectGenetic Phenomena
dc.subjectGenetics and Genomics
dc.subjectMolecular Biology
dc.subjectStructural Biology
dc.titleA systematic survey of an intragenic epistatic landscape [preprint]
dc.typePreprint
dc.source.journaltitlebioRxiv
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2573&amp;context=faculty_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/faculty_pubs/1563
dc.identifier.contextkey12351883
refterms.dateFOA2022-08-23T15:53:21Z
html.description.abstract<p>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 1000 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.</p>
dc.identifier.submissionpathfaculty_pubs/1563
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology


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The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC-ND 4.0 International license.
Except where otherwise noted, this item's license is described as The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. It is made available under a CC-BY-NC-ND 4.0 International license.