Epstein–Barr virus EBER1 and murine gammaherpesvirus TMER4 share conserved in vivo function to promote B cell egress and dissemination
The oncogenic gammaherpesviruses, including human Epstein–Barr virus (EBV), human Kaposi’s sarcoma-associated herpesvirus (KSHV), and murine gammaherpesvirus 68 (MHV68, γHV68, MuHV-4) establish life-long latency in circulating B cells. The precise determinants that mediate in vivo gammaherpesvirus l...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2019-12, Vol.116 (51), p.25392-25394 |
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description | The oncogenic gammaherpesviruses, including human Epstein–Barr virus (EBV), human Kaposi’s sarcoma-associated herpesvirus (KSHV), and murine gammaherpesvirus 68 (MHV68, γHV68, MuHV-4) establish life-long latency in circulating B cells. The precise determinants that mediate in vivo gammaherpesvirus latency and tumorigenesis remain unclear. The EBV-encoded RNAs (EBERs) are among the first noncoding RNAs ever identified and have been the subject of decades of studies; however, their biological roles during in vivo infection remain unknown. Herein, we use a series of refined virus mutants to define the active isoform of MHV68 noncoding RNA TMER4 and demonstrate that EBV EBER1 functionally conserves this activity in vivo to promote egress of infected B cells from lymph nodes into peripheral circulation. |
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The precise determinants that mediate in vivo gammaherpesvirus latency and tumorigenesis remain unclear. The EBV-encoded RNAs (EBERs) are among the first noncoding RNAs ever identified and have been the subject of decades of studies; however, their biological roles during in vivo infection remain unknown. Herein, we use a series of refined virus mutants to define the active isoform of MHV68 noncoding RNA TMER4 and demonstrate that EBV EBER1 functionally conserves this activity in vivo to promote egress of infected B cells from lymph nodes into peripheral circulation.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1915752116</identifier><identifier>PMID: 31796588</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Animals ; Biological Sciences ; BRIEF REPORTS ; Cells, Cultured ; Egress ; Epstein-Barr virus ; Gammaherpesvirinae - genetics ; Herpesviridae Infections - virology ; In vivo methods and tests ; Kaposi's sarcoma ; Latency ; Lymph nodes ; Lymphocytes B ; Mice ; Nucleic Acid Conformation ; Peripheral circulation ; Ribonucleic acid ; RNA ; RNA, Untranslated - chemistry ; RNA, Untranslated - genetics ; RNA, Untranslated - physiology ; RNA, Viral - chemistry ; RNA, Viral - genetics ; RNA, Viral - physiology ; Sarcoma ; Spleen - cytology ; Spleen - virology ; Tumorigenesis ; Virus Latency - genetics ; Virus Release - genetics ; Viruses</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2019-12, Vol.116 (51), p.25392-25394</ispartof><rights>Copyright © 2019 the Author(s). Published by PNAS.</rights><rights>Copyright National Academy of Sciences Dec 17, 2019</rights><rights>Copyright © 2019 the Author(s). 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The precise determinants that mediate in vivo gammaherpesvirus latency and tumorigenesis remain unclear. The EBV-encoded RNAs (EBERs) are among the first noncoding RNAs ever identified and have been the subject of decades of studies; however, their biological roles during in vivo infection remain unknown. 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Wang, Yiping ; Feldman, Emily R. ; Tibbetts, Scott A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-a289ebdc04ecec84a80855e25260838b93303d5baf254acbe113f39065024a603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Biological Sciences</topic><topic>BRIEF REPORTS</topic><topic>Cells, Cultured</topic><topic>Egress</topic><topic>Epstein-Barr virus</topic><topic>Gammaherpesvirinae - genetics</topic><topic>Herpesviridae Infections - virology</topic><topic>In vivo methods and tests</topic><topic>Kaposi's sarcoma</topic><topic>Latency</topic><topic>Lymph nodes</topic><topic>Lymphocytes B</topic><topic>Mice</topic><topic>Nucleic Acid Conformation</topic><topic>Peripheral circulation</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA, Untranslated - chemistry</topic><topic>RNA, Untranslated - genetics</topic><topic>RNA, Untranslated - physiology</topic><topic>RNA, Viral - chemistry</topic><topic>RNA, Viral - genetics</topic><topic>RNA, Viral - physiology</topic><topic>Sarcoma</topic><topic>Spleen - cytology</topic><topic>Spleen - virology</topic><topic>Tumorigenesis</topic><topic>Virus Latency - genetics</topic><topic>Virus Release - genetics</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoffman, Brett A.</creatorcontrib><creatorcontrib>Wang, Yiping</creatorcontrib><creatorcontrib>Feldman, Emily R.</creatorcontrib><creatorcontrib>Tibbetts, Scott 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>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoffman, Brett A.</au><au>Wang, Yiping</au><au>Feldman, Emily R.</au><au>Tibbetts, Scott A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epstein–Barr virus EBER1 and murine gammaherpesvirus TMER4 share conserved in vivo function to promote B cell egress and dissemination</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2019-12-17</date><risdate>2019</risdate><volume>116</volume><issue>51</issue><spage>25392</spage><epage>25394</epage><pages>25392-25394</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The oncogenic gammaherpesviruses, including human Epstein–Barr virus (EBV), human Kaposi’s sarcoma-associated herpesvirus (KSHV), and murine gammaherpesvirus 68 (MHV68, γHV68, MuHV-4) establish life-long latency in circulating B cells. The precise determinants that mediate in vivo gammaherpesvirus latency and tumorigenesis remain unclear. The EBV-encoded RNAs (EBERs) are among the first noncoding RNAs ever identified and have been the subject of decades of studies; however, their biological roles during in vivo infection remain unknown. Herein, we use a series of refined virus mutants to define the active isoform of MHV68 noncoding RNA TMER4 and demonstrate that EBV EBER1 functionally conserves this activity in vivo to promote egress of infected B cells from lymph nodes into peripheral circulation.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>31796588</pmid><doi>10.1073/pnas.1915752116</doi><tpages>3</tpages><orcidid>https://orcid.org/0000-0001-8889-1642</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological Sciences BRIEF REPORTS Cells, Cultured Egress Epstein-Barr virus Gammaherpesvirinae - genetics Herpesviridae Infections - virology In vivo methods and tests Kaposi's sarcoma Latency Lymph nodes Lymphocytes B Mice Nucleic Acid Conformation Peripheral circulation Ribonucleic acid RNA RNA, Untranslated - chemistry RNA, Untranslated - genetics RNA, Untranslated - physiology RNA, Viral - chemistry RNA, Viral - genetics RNA, Viral - physiology Sarcoma Spleen - cytology Spleen - virology Tumorigenesis Virus Latency - genetics Virus Release - genetics Viruses |
title | Epstein–Barr virus EBER1 and murine gammaherpesvirus TMER4 share conserved in vivo function to promote B cell egress and dissemination |
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