Synonymous Mutations at the Beginning of the Influenza A Virus Hemagglutinin Gene Impact Experimental Fitness
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 s...
Gespeichert in:
Veröffentlicht in: | Journal of molecular biology 2018-04, Vol.430 (8), p.1098-1115 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1115 |
---|---|
container_issue | 8 |
container_start_page | 1098 |
container_title | Journal of molecular biology |
container_volume | 430 |
creator | Canale, Aneth S. Venev, Sergey V. Whitfield, Troy W. Caffrey, Daniel R. Marasco, Wayne A. Schiffer, Celia A. Kowalik, Timothy F. Jensen, Jeffrey D. Finberg, Robert W. Zeldovich, Konstantin B. Wang, Jennifer P. Bolon, Daniel N.A. |
description | 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.
[Display omitted]
•Measured experimental fitness effects of mutations at the beginning of HA from IAV•Observed fitness defects for many synonymous mutations•Biochemical analyses indicate that multiple factors contribute to fitness.•Analyses of sequenced isolates indicate host-dependent selection on RNA structure.•Understanding selection on synonymous mutations may require complex models. |
doi_str_mv | 10.1016/j.jmb.2018.02.009 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2007426124</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022283618300809</els_id><sourcerecordid>2007426124</sourcerecordid><originalsourceid>FETCH-LOGICAL-c396t-9eaa8590ab3702903e4957ab2ec0acbc6de9839eaa66f0abb2eecc1c914de1bf3</originalsourceid><addsrcrecordid>eNp9kMtOwzAQRS0EglL4ADbISzYJYyd1Y7ECxKMSiAWPreU4k-IqcUrsIMrX41JgycrS-NyrmUPIEYOUAROni3TRlikHVqTAUwC5RUYMCpkUIiu2yQiA84QXmdgj-94vAGCS5cUu2eMyF2IKkxFpH1euc6u2Gzy9H4IOtnOe6kDDK9ILnFvnrJvTrv4ezFzdDOg-NT2nL7aPmVts9XzeDMFGjt6gi1C71CbQq48l9rZFF3RDr21w6P0B2al14_Hw5x2T5-urp8vb5O7hZnZ5fpeYTIqQSNS6mEjQZTYFLiHDXE6muuRoQJvSiAplka0pIepIxQ80hhnJ8gpZWWdjcrLpXfbd24A-qNZ6g02jHcZLFQeY5lwwnkeUbVDTd973WKtl3Fr3K8VArS2rhYqW1dqyAq6i5Zg5_qkfyharv8Sv1gicbQCMR75b7JU3Fp3ByvZogqo6-0_9F9OOj4Y</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2007426124</pqid></control><display><type>article</type><title>Synonymous Mutations at the Beginning of the Influenza A Virus Hemagglutinin Gene Impact Experimental Fitness</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Canale, Aneth S. ; Venev, Sergey V. ; Whitfield, Troy W. ; Caffrey, Daniel R. ; Marasco, Wayne A. ; Schiffer, Celia A. ; Kowalik, Timothy F. ; Jensen, Jeffrey D. ; Finberg, Robert W. ; Zeldovich, Konstantin B. ; Wang, Jennifer P. ; Bolon, Daniel N.A.</creator><creatorcontrib>Canale, Aneth S. ; Venev, Sergey V. ; Whitfield, Troy W. ; Caffrey, Daniel R. ; Marasco, Wayne A. ; Schiffer, Celia A. ; Kowalik, Timothy F. ; Jensen, Jeffrey D. ; Finberg, Robert W. ; Zeldovich, Konstantin B. ; Wang, Jennifer P. ; Bolon, Daniel N.A.</creatorcontrib><description>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.
[Display omitted]
•Measured experimental fitness effects of mutations at the beginning of HA from IAV•Observed fitness defects for many synonymous mutations•Biochemical analyses indicate that multiple factors contribute to fitness.•Analyses of sequenced isolates indicate host-dependent selection on RNA structure.•Understanding selection on synonymous mutations may require complex models.</description><identifier>ISSN: 0022-2836</identifier><identifier>EISSN: 1089-8638</identifier><identifier>DOI: 10.1016/j.jmb.2018.02.009</identifier><identifier>PMID: 29466705</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Amino Acid Substitution ; Animals ; deep mutational scanning ; Dogs ; Evolution, Molecular ; experimental evolution ; Genetic Fitness ; HEK293 Cells ; Hemagglutinin Glycoproteins, Influenza Virus - chemistry ; Hemagglutinin Glycoproteins, Influenza Virus - genetics ; Humans ; influenza A virus ; Influenza A Virus, H1N1 Subtype - genetics ; Influenza A Virus, H1N1 Subtype - growth & development ; Madin Darby Canine Kidney Cells ; Models, Molecular ; Phylogeny ; RNA Folding ; selection ; Silent Mutation ; Swine ; synonymous mutations ; Virus Replication</subject><ispartof>Journal of molecular biology, 2018-04, Vol.430 (8), p.1098-1115</ispartof><rights>2018</rights><rights>Copyright © 2018. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-9eaa8590ab3702903e4957ab2ec0acbc6de9839eaa66f0abb2eecc1c914de1bf3</citedby><cites>FETCH-LOGICAL-c396t-9eaa8590ab3702903e4957ab2ec0acbc6de9839eaa66f0abb2eecc1c914de1bf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022283618300809$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29466705$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Canale, Aneth S.</creatorcontrib><creatorcontrib>Venev, Sergey V.</creatorcontrib><creatorcontrib>Whitfield, Troy W.</creatorcontrib><creatorcontrib>Caffrey, Daniel R.</creatorcontrib><creatorcontrib>Marasco, Wayne A.</creatorcontrib><creatorcontrib>Schiffer, Celia A.</creatorcontrib><creatorcontrib>Kowalik, Timothy F.</creatorcontrib><creatorcontrib>Jensen, Jeffrey D.</creatorcontrib><creatorcontrib>Finberg, Robert W.</creatorcontrib><creatorcontrib>Zeldovich, Konstantin B.</creatorcontrib><creatorcontrib>Wang, Jennifer P.</creatorcontrib><creatorcontrib>Bolon, Daniel N.A.</creatorcontrib><title>Synonymous Mutations at the Beginning of the Influenza A Virus Hemagglutinin Gene Impact Experimental Fitness</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>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.
[Display omitted]
•Measured experimental fitness effects of mutations at the beginning of HA from IAV•Observed fitness defects for many synonymous mutations•Biochemical analyses indicate that multiple factors contribute to fitness.•Analyses of sequenced isolates indicate host-dependent selection on RNA structure.•Understanding selection on synonymous mutations may require complex models.</description><subject>Amino Acid Substitution</subject><subject>Animals</subject><subject>deep mutational scanning</subject><subject>Dogs</subject><subject>Evolution, Molecular</subject><subject>experimental evolution</subject><subject>Genetic Fitness</subject><subject>HEK293 Cells</subject><subject>Hemagglutinin Glycoproteins, Influenza Virus - chemistry</subject><subject>Hemagglutinin Glycoproteins, Influenza Virus - genetics</subject><subject>Humans</subject><subject>influenza A virus</subject><subject>Influenza A Virus, H1N1 Subtype - genetics</subject><subject>Influenza A Virus, H1N1 Subtype - growth & development</subject><subject>Madin Darby Canine Kidney Cells</subject><subject>Models, Molecular</subject><subject>Phylogeny</subject><subject>RNA Folding</subject><subject>selection</subject><subject>Silent Mutation</subject><subject>Swine</subject><subject>synonymous mutations</subject><subject>Virus Replication</subject><issn>0022-2836</issn><issn>1089-8638</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EglL4ADbISzYJYyd1Y7ECxKMSiAWPreU4k-IqcUrsIMrX41JgycrS-NyrmUPIEYOUAROni3TRlikHVqTAUwC5RUYMCpkUIiu2yQiA84QXmdgj-94vAGCS5cUu2eMyF2IKkxFpH1euc6u2Gzy9H4IOtnOe6kDDK9ILnFvnrJvTrv4ezFzdDOg-NT2nL7aPmVts9XzeDMFGjt6gi1C71CbQq48l9rZFF3RDr21w6P0B2al14_Hw5x2T5-urp8vb5O7hZnZ5fpeYTIqQSNS6mEjQZTYFLiHDXE6muuRoQJvSiAplka0pIepIxQ80hhnJ8gpZWWdjcrLpXfbd24A-qNZ6g02jHcZLFQeY5lwwnkeUbVDTd973WKtl3Fr3K8VArS2rhYqW1dqyAq6i5Zg5_qkfyharv8Sv1gicbQCMR75b7JU3Fp3ByvZogqo6-0_9F9OOj4Y</recordid><startdate>20180413</startdate><enddate>20180413</enddate><creator>Canale, Aneth S.</creator><creator>Venev, Sergey V.</creator><creator>Whitfield, Troy W.</creator><creator>Caffrey, Daniel R.</creator><creator>Marasco, Wayne A.</creator><creator>Schiffer, Celia A.</creator><creator>Kowalik, Timothy F.</creator><creator>Jensen, Jeffrey D.</creator><creator>Finberg, Robert W.</creator><creator>Zeldovich, Konstantin B.</creator><creator>Wang, Jennifer P.</creator><creator>Bolon, Daniel N.A.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20180413</creationdate><title>Synonymous Mutations at the Beginning of the Influenza A Virus Hemagglutinin Gene Impact Experimental Fitness</title><author>Canale, Aneth S. ; Venev, Sergey V. ; Whitfield, Troy W. ; Caffrey, Daniel R. ; Marasco, Wayne A. ; Schiffer, Celia A. ; Kowalik, Timothy F. ; Jensen, Jeffrey D. ; Finberg, Robert W. ; Zeldovich, Konstantin B. ; Wang, Jennifer P. ; Bolon, Daniel N.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-9eaa8590ab3702903e4957ab2ec0acbc6de9839eaa66f0abb2eecc1c914de1bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Amino Acid Substitution</topic><topic>Animals</topic><topic>deep mutational scanning</topic><topic>Dogs</topic><topic>Evolution, Molecular</topic><topic>experimental evolution</topic><topic>Genetic Fitness</topic><topic>HEK293 Cells</topic><topic>Hemagglutinin Glycoproteins, Influenza Virus - chemistry</topic><topic>Hemagglutinin Glycoproteins, Influenza Virus - genetics</topic><topic>Humans</topic><topic>influenza A virus</topic><topic>Influenza A Virus, H1N1 Subtype - genetics</topic><topic>Influenza A Virus, H1N1 Subtype - growth & development</topic><topic>Madin Darby Canine Kidney Cells</topic><topic>Models, Molecular</topic><topic>Phylogeny</topic><topic>RNA Folding</topic><topic>selection</topic><topic>Silent Mutation</topic><topic>Swine</topic><topic>synonymous mutations</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Canale, Aneth S.</creatorcontrib><creatorcontrib>Venev, Sergey V.</creatorcontrib><creatorcontrib>Whitfield, Troy W.</creatorcontrib><creatorcontrib>Caffrey, Daniel R.</creatorcontrib><creatorcontrib>Marasco, Wayne A.</creatorcontrib><creatorcontrib>Schiffer, Celia A.</creatorcontrib><creatorcontrib>Kowalik, Timothy F.</creatorcontrib><creatorcontrib>Jensen, Jeffrey D.</creatorcontrib><creatorcontrib>Finberg, Robert W.</creatorcontrib><creatorcontrib>Zeldovich, Konstantin B.</creatorcontrib><creatorcontrib>Wang, Jennifer P.</creatorcontrib><creatorcontrib>Bolon, Daniel N.A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Canale, Aneth S.</au><au>Venev, Sergey V.</au><au>Whitfield, Troy W.</au><au>Caffrey, Daniel R.</au><au>Marasco, Wayne A.</au><au>Schiffer, Celia A.</au><au>Kowalik, Timothy F.</au><au>Jensen, Jeffrey D.</au><au>Finberg, Robert W.</au><au>Zeldovich, Konstantin B.</au><au>Wang, Jennifer P.</au><au>Bolon, Daniel N.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synonymous Mutations at the Beginning of the Influenza A Virus Hemagglutinin Gene Impact Experimental Fitness</atitle><jtitle>Journal of molecular biology</jtitle><addtitle>J Mol Biol</addtitle><date>2018-04-13</date><risdate>2018</risdate><volume>430</volume><issue>8</issue><spage>1098</spage><epage>1115</epage><pages>1098-1115</pages><issn>0022-2836</issn><eissn>1089-8638</eissn><abstract>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.
[Display omitted]
•Measured experimental fitness effects of mutations at the beginning of HA from IAV•Observed fitness defects for many synonymous mutations•Biochemical analyses indicate that multiple factors contribute to fitness.•Analyses of sequenced isolates indicate host-dependent selection on RNA structure.•Understanding selection on synonymous mutations may require complex models.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>29466705</pmid><doi>10.1016/j.jmb.2018.02.009</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-2836 |
ispartof | Journal of molecular biology, 2018-04, Vol.430 (8), p.1098-1115 |
issn | 0022-2836 1089-8638 |
language | eng |
recordid | cdi_proquest_miscellaneous_2007426124 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Amino Acid Substitution Animals deep mutational scanning Dogs Evolution, Molecular experimental evolution Genetic Fitness HEK293 Cells Hemagglutinin Glycoproteins, Influenza Virus - chemistry Hemagglutinin Glycoproteins, Influenza Virus - genetics Humans influenza A virus Influenza A Virus, H1N1 Subtype - genetics Influenza A Virus, H1N1 Subtype - growth & development Madin Darby Canine Kidney Cells Models, Molecular Phylogeny RNA Folding selection Silent Mutation Swine synonymous mutations Virus Replication |
title | Synonymous Mutations at the Beginning of the Influenza A Virus Hemagglutinin Gene Impact Experimental Fitness |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T18%3A07%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synonymous%20Mutations%20at%20the%20Beginning%20of%20the%20Influenza%20A%20Virus%20Hemagglutinin%20Gene%20Impact%20Experimental%20Fitness&rft.jtitle=Journal%20of%20molecular%20biology&rft.au=Canale,%20Aneth%20S.&rft.date=2018-04-13&rft.volume=430&rft.issue=8&rft.spage=1098&rft.epage=1115&rft.pages=1098-1115&rft.issn=0022-2836&rft.eissn=1089-8638&rft_id=info:doi/10.1016/j.jmb.2018.02.009&rft_dat=%3Cproquest_cross%3E2007426124%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2007426124&rft_id=info:pmid/29466705&rft_els_id=S0022283618300809&rfr_iscdi=true |