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SERINC proteins potentiate antiviral type I IFN production and proinflammatory signaling pathways
The SERINC (serine incorporator) proteins are host restriction factors that inhibit infection by HIV through their incorporation into virions. Here, we found that SERINC3 and SERINC5 exhibited additional antiviral activities by enhancing the expression of genes encoding type I interferons (IFNs) and...
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Published in: | Science signaling 2021-09, Vol.14 (700), p.eabc7611-eabc7611 |
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description | The SERINC (serine incorporator) proteins are host restriction factors that inhibit infection by HIV through their incorporation into virions. Here, we found that SERINC3 and SERINC5 exhibited additional antiviral activities by enhancing the expression of genes encoding type I interferons (IFNs) and nuclear factor κB (NF-κB) signaling. SERINC5 interacted with the outer mitochondrial membrane protein MAVS (mitochondrial antiviral signaling) and the E3 ubiquitin ligase and adaptor protein TRAF6, resulting in MAVS aggregation and polyubiquitylation of TRAF6. Knockdown of SERINC5 in target cells increased single-round HIV-1 infectivity, as well as infection by recombinant vesicular stomatitis virus (rVSV) bearing VSV-G or Ebola virus (EBOV) glycoproteins. Infection by an endemic Asian strain of Zika virus (ZIKV), FSS13025, was also enhanced by SERINC5 knockdown, suggesting that SERINC5 has direct antiviral activities in host cells in addition to the indirect inhibition mediated by its incorporation into virions. Further experiments suggested that the antiviral activity of SERINC5 was type I IFN–dependent. Together, these results highlight a previously uncharacterized function of SERINC proteins in promoting NF-κB inflammatory signaling and type I IFN production, thus contributing to its antiviral activities. |
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Here, we found that SERINC3 and SERINC5 exhibited additional antiviral activities by enhancing the expression of genes encoding type I interferons (IFNs) and nuclear factor κB (NF-κB) signaling. SERINC5 interacted with the outer mitochondrial membrane protein MAVS (mitochondrial antiviral signaling) and the E3 ubiquitin ligase and adaptor protein TRAF6, resulting in MAVS aggregation and polyubiquitylation of TRAF6. Knockdown of SERINC5 in target cells increased single-round HIV-1 infectivity, as well as infection by recombinant vesicular stomatitis virus (rVSV) bearing VSV-G or Ebola virus (EBOV) glycoproteins. Infection by an endemic Asian strain of Zika virus (ZIKV), FSS13025, was also enhanced by SERINC5 knockdown, suggesting that SERINC5 has direct antiviral activities in host cells in addition to the indirect inhibition mediated by its incorporation into virions. Further experiments suggested that the antiviral activity of SERINC5 was type I IFN–dependent. Together, these results highlight a previously uncharacterized function of SERINC proteins in promoting NF-κB inflammatory signaling and type I IFN production, thus contributing to its antiviral activities.</description><identifier>ISSN: 1945-0877</identifier><identifier>EISSN: 1937-9145</identifier><identifier>DOI: 10.1126/scisignal.abc7611</identifier><identifier>PMID: 34520227</identifier><language>eng</language><publisher>United States: The American Association for the Advancement of Science</publisher><subject>Adapters ; Adaptor proteins ; Antiviral activity ; Antiviral Agents ; Cytokines ; Gene expression ; Genes ; Glycoproteins ; HIV ; Human immunodeficiency virus ; Incorporation ; Infections ; Infectivity ; Inflammation ; Interferon ; Membrane proteins ; Membranes ; Mitochondria ; NF-κB protein ; Oligomerization ; Proteins ; Signal Transduction ; Signaling ; Stomatitis ; TRAF6 protein ; Transcription activation ; Ubiquitin ; Ubiquitin-protein ligase ; Vector-borne diseases ; Viral diseases ; Viral infections ; Virions ; Viruses</subject><ispartof>Science signaling, 2021-09, Vol.14 (700), p.eabc7611-eabc7611</ispartof><rights>Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-325a9b9db931a085edbbb34162df0be0e45a8b44ece6bcffd0e1233ae293d9fa3</citedby><cites>FETCH-LOGICAL-c394t-325a9b9db931a085edbbb34162df0be0e45a8b44ece6bcffd0e1233ae293d9fa3</cites><orcidid>0000-0003-4423-3634 ; 0000-0002-0775-6623</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34520227$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zeng, Cong</creatorcontrib><creatorcontrib>Waheed, Abdul A</creatorcontrib><creatorcontrib>Li, Tianliang</creatorcontrib><creatorcontrib>Yu, Jingyou</creatorcontrib><creatorcontrib>Zheng, Yi-Min</creatorcontrib><creatorcontrib>Yount, Jacob S</creatorcontrib><creatorcontrib>Wen, Haitao</creatorcontrib><creatorcontrib>Freed, Eric O</creatorcontrib><creatorcontrib>Liu, Shan-Lu</creatorcontrib><title>SERINC proteins potentiate antiviral type I IFN production and proinflammatory signaling pathways</title><title>Science signaling</title><addtitle>Sci Signal</addtitle><description>The SERINC (serine incorporator) proteins are host restriction factors that inhibit infection by HIV through their incorporation into virions. Here, we found that SERINC3 and SERINC5 exhibited additional antiviral activities by enhancing the expression of genes encoding type I interferons (IFNs) and nuclear factor κB (NF-κB) signaling. SERINC5 interacted with the outer mitochondrial membrane protein MAVS (mitochondrial antiviral signaling) and the E3 ubiquitin ligase and adaptor protein TRAF6, resulting in MAVS aggregation and polyubiquitylation of TRAF6. Knockdown of SERINC5 in target cells increased single-round HIV-1 infectivity, as well as infection by recombinant vesicular stomatitis virus (rVSV) bearing VSV-G or Ebola virus (EBOV) glycoproteins. Infection by an endemic Asian strain of Zika virus (ZIKV), FSS13025, was also enhanced by SERINC5 knockdown, suggesting that SERINC5 has direct antiviral activities in host cells in addition to the indirect inhibition mediated by its incorporation into virions. Further experiments suggested that the antiviral activity of SERINC5 was type I IFN–dependent. Together, these results highlight a previously uncharacterized function of SERINC proteins in promoting NF-κB inflammatory signaling and type I IFN production, thus contributing to its antiviral activities.</description><subject>Adapters</subject><subject>Adaptor proteins</subject><subject>Antiviral activity</subject><subject>Antiviral Agents</subject><subject>Cytokines</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Glycoproteins</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Incorporation</subject><subject>Infections</subject><subject>Infectivity</subject><subject>Inflammation</subject><subject>Interferon</subject><subject>Membrane proteins</subject><subject>Membranes</subject><subject>Mitochondria</subject><subject>NF-κB protein</subject><subject>Oligomerization</subject><subject>Proteins</subject><subject>Signal Transduction</subject><subject>Signaling</subject><subject>Stomatitis</subject><subject>TRAF6 protein</subject><subject>Transcription activation</subject><subject>Ubiquitin</subject><subject>Ubiquitin-protein ligase</subject><subject>Vector-borne diseases</subject><subject>Viral diseases</subject><subject>Viral infections</subject><subject>Virions</subject><subject>Viruses</subject><issn>1945-0877</issn><issn>1937-9145</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVUdtKw0AQXUSxtfoBvkjA59S95bIvgpRWC6WCl-dlNtm0W9Ik7m4q_XsTWos-nRnmzJkzHIRuCR4TQuMHlxlnVhWUY1BZEhNyhoZEsCQUhEfnfc2jEKdJMkBXzm0wjgml4hINGI8opjQZInifvs2Xk6CxtdemckHTYeUNeB1AhztjoQz8vtHBPJjPlj0xbzNv6qqb531rqqKE7RZ8bffBwY-pVkEDfv0Ne3eNLgoonb454gh9zqYfk5dw8fo8nzwtwowJ7kNGIxBK5EowAjiNdK6UYpzENC-w0ljzCFLFuc50rLKiyLEmlDHQVLBcFMBG6PGg27Rqq_Os-6KzLhtrtmD3sgYj_08qs5areidFxEWCSSdwfxSw9VernZeburXdN07SmKU4EQnrWeTAymztnNXF6QLBsk9FnlKRx1S6nbu_1k4bvzGwH0ZDj5k</recordid><startdate>20210914</startdate><enddate>20210914</enddate><creator>Zeng, Cong</creator><creator>Waheed, Abdul A</creator><creator>Li, Tianliang</creator><creator>Yu, Jingyou</creator><creator>Zheng, Yi-Min</creator><creator>Yount, Jacob S</creator><creator>Wen, Haitao</creator><creator>Freed, Eric O</creator><creator>Liu, Shan-Lu</creator><general>The American Association for the Advancement of Science</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>7QL</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>JQ2</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4423-3634</orcidid><orcidid>https://orcid.org/0000-0002-0775-6623</orcidid></search><sort><creationdate>20210914</creationdate><title>SERINC proteins potentiate antiviral type I IFN production and proinflammatory signaling pathways</title><author>Zeng, Cong ; Waheed, Abdul A ; Li, Tianliang ; Yu, Jingyou ; Zheng, Yi-Min ; Yount, Jacob S ; Wen, Haitao ; Freed, Eric O ; Liu, Shan-Lu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-325a9b9db931a085edbbb34162df0be0e45a8b44ece6bcffd0e1233ae293d9fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adapters</topic><topic>Adaptor proteins</topic><topic>Antiviral activity</topic><topic>Antiviral Agents</topic><topic>Cytokines</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Glycoproteins</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Incorporation</topic><topic>Infections</topic><topic>Infectivity</topic><topic>Inflammation</topic><topic>Interferon</topic><topic>Membrane proteins</topic><topic>Membranes</topic><topic>Mitochondria</topic><topic>NF-κB protein</topic><topic>Oligomerization</topic><topic>Proteins</topic><topic>Signal Transduction</topic><topic>Signaling</topic><topic>Stomatitis</topic><topic>TRAF6 protein</topic><topic>Transcription activation</topic><topic>Ubiquitin</topic><topic>Ubiquitin-protein ligase</topic><topic>Vector-borne diseases</topic><topic>Viral diseases</topic><topic>Viral infections</topic><topic>Virions</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zeng, Cong</creatorcontrib><creatorcontrib>Waheed, Abdul A</creatorcontrib><creatorcontrib>Li, Tianliang</creatorcontrib><creatorcontrib>Yu, Jingyou</creatorcontrib><creatorcontrib>Zheng, Yi-Min</creatorcontrib><creatorcontrib>Yount, Jacob S</creatorcontrib><creatorcontrib>Wen, Haitao</creatorcontrib><creatorcontrib>Freed, Eric O</creatorcontrib><creatorcontrib>Liu, Shan-Lu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Science signaling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zeng, Cong</au><au>Waheed, Abdul A</au><au>Li, Tianliang</au><au>Yu, Jingyou</au><au>Zheng, Yi-Min</au><au>Yount, Jacob S</au><au>Wen, Haitao</au><au>Freed, Eric O</au><au>Liu, Shan-Lu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SERINC proteins potentiate antiviral type I IFN production and proinflammatory signaling pathways</atitle><jtitle>Science signaling</jtitle><addtitle>Sci Signal</addtitle><date>2021-09-14</date><risdate>2021</risdate><volume>14</volume><issue>700</issue><spage>eabc7611</spage><epage>eabc7611</epage><pages>eabc7611-eabc7611</pages><issn>1945-0877</issn><eissn>1937-9145</eissn><abstract>The SERINC (serine incorporator) proteins are host restriction factors that inhibit infection by HIV through their incorporation into virions. 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subjects | Adapters Adaptor proteins Antiviral activity Antiviral Agents Cytokines Gene expression Genes Glycoproteins HIV Human immunodeficiency virus Incorporation Infections Infectivity Inflammation Interferon Membrane proteins Membranes Mitochondria NF-κB protein Oligomerization Proteins Signal Transduction Signaling Stomatitis TRAF6 protein Transcription activation Ubiquitin Ubiquitin-protein ligase Vector-borne diseases Viral diseases Viral infections Virions Viruses |
title | SERINC proteins potentiate antiviral type I IFN production and proinflammatory signaling pathways |
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