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dc.contributor.authorCanale, Aneth S.
dc.contributor.authorVenev, Sergey V
dc.contributor.authorWhitfield, Troy W.
dc.contributor.authorCaffrey, Daniel R.
dc.contributor.authorMarasco, Wayne A.
dc.contributor.authorSchiffer, Celia A.
dc.contributor.authorKowalik, Timothy F.
dc.contributor.authorJensen, Jeffrey D.
dc.contributor.authorFinberg, Robert W.
dc.contributor.authorZeldovich, Konstantin B.
dc.contributor.authorWang, Jennifer P.
dc.contributor.authorBolon, Daniel N A
dc.date2022-08-11T08:10:52.000
dc.date.accessioned2022-08-23T17:23:05Z
dc.date.available2022-08-23T17:23:05Z
dc.date.issued2018-04-13
dc.date.submitted2018-10-19
dc.identifier.citation<p>J Mol Biol. 2018 Apr 13;430(8):1098-1115. doi: 10.1016/j.jmb.2018.02.009. Epub 2018 Feb 18. <a href="https://doi.org/10.1016/j.jmb.2018.02.009">Link to article on publisher's site</a></p>
dc.identifier.issn0022-2836 (Linking)
dc.identifier.doi10.1016/j.jmb.2018.02.009
dc.identifier.pmid29466705
dc.identifier.urihttp://hdl.handle.net/20.500.14038/48881
dc.description.abstractThe fitness effects of synonymous mutations can provide insights into biological and evolutionary mechanisms. We analyzed the experimental fitness effects of all single-nucleotide mutations, including synonymous substitutions, at the beginning of the influenza A virus hemagglutinin (HA) gene. Many synonymous substitutions were deleterious both in bulk competition and for individually isolated clones. Investigating protein and RNA levels of a subset of individually expressed HA variants revealed that multiple biochemical properties contribute to the observed experimental fitness effects. Our results indicate that a structural element in the HA segment viral RNA may influence fitness. Examination of naturally evolved sequences in human hosts indicates a preference for the unfolded state of this structural element compared to that found in swine hosts. Our overall results reveal that synonymous mutations may have greater fitness consequences than indicated by simple models of sequence conservation, and we discuss the implications of this finding for commonly used evolutionary tests and analyses.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=29466705&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/j.jmb.2018.02.009
dc.subjectdeep mutational scanning
dc.subjectexperimental evolution
dc.subjectinfluenza A virus
dc.subjectselection
dc.subjectsynonymous mutations
dc.subjectBiochemistry
dc.subjectEcology and Evolutionary Biology
dc.subjectGenetic Phenomena
dc.subjectMedicinal Chemistry and Pharmaceutics
dc.subjectMedicinal-Pharmaceutical Chemistry
dc.subjectMolecular Biology
dc.subjectNucleic Acids, Nucleotides, and Nucleosides
dc.subjectStructural Biology
dc.titleSynonymous Mutations at the Beginning of the Influenza A Virus Hemagglutinin Gene Impact Experimental Fitness
dc.typeJournal Article
dc.source.journaltitleJournal of molecular biology
dc.source.volume430
dc.source.issue8
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/schiffer/27
dc.identifier.contextkey13122626
html.description.abstract<p>The fitness effects of synonymous mutations can provide insights into biological and evolutionary mechanisms. We analyzed the experimental fitness effects of all single-nucleotide mutations, including synonymous substitutions, at the beginning of the influenza A virus hemagglutinin (HA) gene. Many synonymous substitutions were deleterious both in bulk competition and for individually isolated clones. Investigating protein and RNA levels of a subset of individually expressed HA variants revealed that multiple biochemical properties contribute to the observed experimental fitness effects. Our results indicate that a structural element in the HA segment viral RNA may influence fitness. Examination of naturally evolved sequences in human hosts indicates a preference for the unfolded state of this structural element compared to that found in swine hosts. Our overall results reveal that synonymous mutations may have greater fitness consequences than indicated by simple models of sequence conservation, and we discuss the implications of this finding for commonly used evolutionary tests and analyses.</p>
dc.identifier.submissionpathschiffer/27
dc.contributor.departmentSchiffer Lab
dc.contributor.departmentDepartment of Microbiology and Physiological Systems
dc.contributor.departmentDepartment of Medicine
dc.contributor.departmentProgram in Bioinformatics and Integrative Biology
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pages1098-1115


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