Redundancy complicates the definition of essential genes for vaccinia virus
Vaccinia virus (VACV) genes are characterized as either essential or non-essential for growth in culture. It seems intuitively obvious that if a gene can be deleted without imparting a growth defect in vitro it does not have a function related to basic replication or spread. However, this interpreta...
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Veröffentlicht in: | Journal of general virology 2015-11, Vol.96 (11), p.3326-3337 |
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description | Vaccinia virus (VACV) genes are characterized as either essential or non-essential for growth in culture. It seems intuitively obvious that if a gene can be deleted without imparting a growth defect in vitro it does not have a function related to basic replication or spread. However, this interpretation relies on the untested assumption that there is no redundancy across the genes that have roles in growth in cell culture. First, we provide a comprehensive summary of the literature that describes the essential genes of VACV. Next, we looked for interactions between large blocks of non-essential genes located at the ends of the genome by investigating sets of VACVs with large deletions at the genomic termini. Viruses with deletions at either end of the genome behaved as expected, exhibiting only mild or host-range defects. In contrast, combining deletions at both ends of the genome for the VACV Western Reserve (WR) strain caused a devastating growth defect on all cell lines tested. Unexpectedly, we found that the well-studied VACV growth factor homologue encoded by C11R has a role in growth in vitro that is exposed when 42 genes are absent from the left end of the VACV WR genome. These results demonstrate that some non-essential genes contribute to basic viral growth, but redundancy means these functions are not revealed by single-gene-deletion mutants. |
doi_str_mv | 10.1099/jgv.0.000266 |
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It seems intuitively obvious that if a gene can be deleted without imparting a growth defect in vitro it does not have a function related to basic replication or spread. However, this interpretation relies on the untested assumption that there is no redundancy across the genes that have roles in growth in cell culture. First, we provide a comprehensive summary of the literature that describes the essential genes of VACV. Next, we looked for interactions between large blocks of non-essential genes located at the ends of the genome by investigating sets of VACVs with large deletions at the genomic termini. Viruses with deletions at either end of the genome behaved as expected, exhibiting only mild or host-range defects. In contrast, combining deletions at both ends of the genome for the VACV Western Reserve (WR) strain caused a devastating growth defect on all cell lines tested. Unexpectedly, we found that the well-studied VACV growth factor homologue encoded by C11R has a role in growth in vitro that is exposed when 42 genes are absent from the left end of the VACV WR genome. These results demonstrate that some non-essential genes contribute to basic viral growth, but redundancy means these functions are not revealed by single-gene-deletion mutants.</description><identifier>ISSN: 0022-1317</identifier><identifier>EISSN: 1465-2099</identifier><identifier>DOI: 10.1099/jgv.0.000266</identifier><identifier>PMID: 26290187</identifier><language>eng</language><publisher>England: Microbiology Society</publisher><subject>Genes, Essential ; Genome, Viral ; Humans ; Vaccinia - virology ; Vaccinia virus - genetics ; Vaccinia virus - growth & development ; Vaccinia virus - physiology ; Viral Proteins - genetics ; Viral Proteins - metabolism ; Virus Replication</subject><ispartof>Journal of general virology, 2015-11, Vol.96 (11), p.3326-3337</ispartof><rights>2015 The Authors 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-bb413aba09a334546a15b864005a10f256f6882e16d7e2fb8035a546080cbc263</citedby><cites>FETCH-LOGICAL-c384t-bb413aba09a334546a15b864005a10f256f6882e16d7e2fb8035a546080cbc263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3744,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26290187$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dobson, Bianca M</creatorcontrib><creatorcontrib>Tscharke, David C</creatorcontrib><title>Redundancy complicates the definition of essential genes for vaccinia virus</title><title>Journal of general virology</title><addtitle>J Gen Virol</addtitle><description>Vaccinia virus (VACV) genes are characterized as either essential or non-essential for growth in culture. It seems intuitively obvious that if a gene can be deleted without imparting a growth defect in vitro it does not have a function related to basic replication or spread. However, this interpretation relies on the untested assumption that there is no redundancy across the genes that have roles in growth in cell culture. First, we provide a comprehensive summary of the literature that describes the essential genes of VACV. Next, we looked for interactions between large blocks of non-essential genes located at the ends of the genome by investigating sets of VACVs with large deletions at the genomic termini. Viruses with deletions at either end of the genome behaved as expected, exhibiting only mild or host-range defects. In contrast, combining deletions at both ends of the genome for the VACV Western Reserve (WR) strain caused a devastating growth defect on all cell lines tested. Unexpectedly, we found that the well-studied VACV growth factor homologue encoded by C11R has a role in growth in vitro that is exposed when 42 genes are absent from the left end of the VACV WR genome. These results demonstrate that some non-essential genes contribute to basic viral growth, but redundancy means these functions are not revealed by single-gene-deletion mutants.</description><subject>Genes, Essential</subject><subject>Genome, Viral</subject><subject>Humans</subject><subject>Vaccinia - virology</subject><subject>Vaccinia virus - genetics</subject><subject>Vaccinia virus - growth & development</subject><subject>Vaccinia virus - physiology</subject><subject>Viral Proteins - genetics</subject><subject>Viral Proteins - metabolism</subject><subject>Virus Replication</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE1Lw0AQhhdRbK3ePEuOHkyd_U4ughS_sCCInpfNZtNuSbM1mwT6711pLXoamPfhneFB6BLDFEOe364WwxSmAECEOEJjzARPSQyO0TjuSIopliN0FsIKADPG5SkaEUFywJkco9d3W_ZNqRuzTYxfb2pndGdD0i1tUtrKNa5zvkl8ldgQbNM5XScL20Si8m0yaGMiopPBtX04RyeVroO92M8J-nx8-Jg9p_O3p5fZ_Tw1NGNdWhQMU11oyDWljDOhMS8ywQC4xlARLiqRZcRiUUpLqiIDynXEIANTGCLoBN3tejd9sbaliW-1ulab1q11u1VeO_U_adxSLfygeC4JpRALrvcFrf_qbejU2gVj61o31vdBYSllnklgPKI3O9S0PoTWVoczGNSPfxX9K1A7_xG_-vvaAf4VTr8BX4qB7w</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Dobson, Bianca M</creator><creator>Tscharke, David C</creator><general>Microbiology Society</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><scope>5PM</scope></search><sort><creationdate>20151101</creationdate><title>Redundancy complicates the definition of essential genes for vaccinia virus</title><author>Dobson, Bianca M ; Tscharke, David C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-bb413aba09a334546a15b864005a10f256f6882e16d7e2fb8035a546080cbc263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Genes, Essential</topic><topic>Genome, Viral</topic><topic>Humans</topic><topic>Vaccinia - virology</topic><topic>Vaccinia virus - genetics</topic><topic>Vaccinia virus - growth & development</topic><topic>Vaccinia virus - physiology</topic><topic>Viral Proteins - genetics</topic><topic>Viral Proteins - metabolism</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dobson, Bianca M</creatorcontrib><creatorcontrib>Tscharke, David C</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dobson, Bianca M</au><au>Tscharke, David C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Redundancy complicates the definition of essential genes for vaccinia virus</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>96</volume><issue>11</issue><spage>3326</spage><epage>3337</epage><pages>3326-3337</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><abstract>Vaccinia virus (VACV) genes are characterized as either essential or non-essential for growth in culture. It seems intuitively obvious that if a gene can be deleted without imparting a growth defect in vitro it does not have a function related to basic replication or spread. However, this interpretation relies on the untested assumption that there is no redundancy across the genes that have roles in growth in cell culture. First, we provide a comprehensive summary of the literature that describes the essential genes of VACV. Next, we looked for interactions between large blocks of non-essential genes located at the ends of the genome by investigating sets of VACVs with large deletions at the genomic termini. Viruses with deletions at either end of the genome behaved as expected, exhibiting only mild or host-range defects. In contrast, combining deletions at both ends of the genome for the VACV Western Reserve (WR) strain caused a devastating growth defect on all cell lines tested. Unexpectedly, we found that the well-studied VACV growth factor homologue encoded by C11R has a role in growth in vitro that is exposed when 42 genes are absent from the left end of the VACV WR genome. These results demonstrate that some non-essential genes contribute to basic viral growth, but redundancy means these functions are not revealed by single-gene-deletion mutants.</abstract><cop>England</cop><pub>Microbiology Society</pub><pmid>26290187</pmid><doi>10.1099/jgv.0.000266</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Genes, Essential Genome, Viral Humans Vaccinia - virology Vaccinia virus - genetics Vaccinia virus - growth & development Vaccinia virus - physiology Viral Proteins - genetics Viral Proteins - metabolism Virus Replication |
title | Redundancy complicates the definition of essential genes for vaccinia virus |
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