DDX5 facilitates HIV-1 replication as a cellular co-factor of Rev
HIV-1 Rev plays an important role in the late phase of HIV-1 replication, which facilitates export of unspliced viral mRNAs from the nucleus to cytoplasm in infected cells. Recent studies have shown that DDX1 and DDX3 are co-factors of Rev for the export of HIV-1 transcripts. In this report, we have...
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description | HIV-1 Rev plays an important role in the late phase of HIV-1 replication, which facilitates export of unspliced viral mRNAs from the nucleus to cytoplasm in infected cells. Recent studies have shown that DDX1 and DDX3 are co-factors of Rev for the export of HIV-1 transcripts. In this report, we have demonstrated that DDX5 (p68), which is a multifunctional DEAD-box RNA helicase, functions as a new cellular co-factor of HIV-1 Rev. We found that DDX5 affects Rev function through the Rev-RRE axis and subsequently enhances HIV-1 replication. Confocal microscopy and co-immunoprecipitation analysis indicated that DDX5 binds to Rev and this interaction is largely dependent on RNA. If the DEAD-box motif of DDX5 is mutated, DDX5 loses almost all of its ability to bind to Rev, indicating that the DEAD-box motif of DDX5 is required for the interaction between DDX5 and Rev. Our data indicate that interference of DDX5-Rev interaction could reduce HIV-1 replication and potentially provide a new molecular target for anti-HIV-1 therapeutics. |
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Recent studies have shown that DDX1 and DDX3 are co-factors of Rev for the export of HIV-1 transcripts. In this report, we have demonstrated that DDX5 (p68), which is a multifunctional DEAD-box RNA helicase, functions as a new cellular co-factor of HIV-1 Rev. We found that DDX5 affects Rev function through the Rev-RRE axis and subsequently enhances HIV-1 replication. Confocal microscopy and co-immunoprecipitation analysis indicated that DDX5 binds to Rev and this interaction is largely dependent on RNA. If the DEAD-box motif of DDX5 is mutated, DDX5 loses almost all of its ability to bind to Rev, indicating that the DEAD-box motif of DDX5 is required for the interaction between DDX5 and Rev. Our data indicate that interference of DDX5-Rev interaction could reduce HIV-1 replication and potentially provide a new molecular target for anti-HIV-1 therapeutics.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0065040</identifier><identifier>PMID: 23741449</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Active Transport, Cell Nucleus ; Antiviral agents ; Biology ; Biosynthesis ; Cell Line ; Confocal microscopy ; Cytoplasm ; DEAD-box RNA Helicases - genetics ; DEAD-box RNA Helicases - metabolism ; Deoxyribonucleic acid ; Disease control ; DNA ; DNA helicase ; Education ; Exports ; Gene Expression ; Genes, Reporter ; Hematology ; Hepatitis ; HIV ; HIV-1 - physiology ; Human immunodeficiency virus ; Humans ; Immunoprecipitation ; Infectious diseases ; Laboratories ; Medicine ; Microscopy ; Nuclei ; Nuclei (cytology) ; Protein Binding ; Proteins ; Replication ; Response Elements ; rev Gene Products, Human Immunodeficiency Virus - metabolism ; Ribonucleic acid ; RNA ; RNA helicase ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Tropical diseases ; Virology ; Virus Replication</subject><ispartof>PloS one, 2013-05, Vol.8 (5), p.e65040-e65040</ispartof><rights>2013 Zhou et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Zhou et al 2013 Zhou et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-2c84154df32f363afc783a101f100f813fd472d6ccc0d67995b473f96180bff53</citedby><cites>FETCH-LOGICAL-c526t-2c84154df32f363afc783a101f100f813fd472d6ccc0d67995b473f96180bff53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669200/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3669200/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2929,23868,27926,27927,53793,53795</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23741449$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Vartanian, Jean-Pierre</contributor><creatorcontrib>Zhou, Xiuxia</creatorcontrib><creatorcontrib>Luo, Juan</creatorcontrib><creatorcontrib>Mills, Lisa</creatorcontrib><creatorcontrib>Wu, Shuangxin</creatorcontrib><creatorcontrib>Pan, Ting</creatorcontrib><creatorcontrib>Geng, Guannan</creatorcontrib><creatorcontrib>Zhang, Jim</creatorcontrib><creatorcontrib>Luo, Haihua</creatorcontrib><creatorcontrib>Liu, Chao</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><title>DDX5 facilitates HIV-1 replication as a cellular co-factor of Rev</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>HIV-1 Rev plays an important role in the late phase of HIV-1 replication, which facilitates export of unspliced viral mRNAs from the nucleus to cytoplasm in infected cells. Recent studies have shown that DDX1 and DDX3 are co-factors of Rev for the export of HIV-1 transcripts. In this report, we have demonstrated that DDX5 (p68), which is a multifunctional DEAD-box RNA helicase, functions as a new cellular co-factor of HIV-1 Rev. We found that DDX5 affects Rev function through the Rev-RRE axis and subsequently enhances HIV-1 replication. Confocal microscopy and co-immunoprecipitation analysis indicated that DDX5 binds to Rev and this interaction is largely dependent on RNA. If the DEAD-box motif of DDX5 is mutated, DDX5 loses almost all of its ability to bind to Rev, indicating that the DEAD-box motif of DDX5 is required for the interaction between DDX5 and Rev. Our data indicate that interference of DDX5-Rev interaction could reduce HIV-1 replication and potentially provide a new molecular target for anti-HIV-1 therapeutics.</description><subject>Active Transport, Cell Nucleus</subject><subject>Antiviral agents</subject><subject>Biology</subject><subject>Biosynthesis</subject><subject>Cell Line</subject><subject>Confocal microscopy</subject><subject>Cytoplasm</subject><subject>DEAD-box RNA Helicases - genetics</subject><subject>DEAD-box RNA Helicases - metabolism</subject><subject>Deoxyribonucleic acid</subject><subject>Disease control</subject><subject>DNA</subject><subject>DNA helicase</subject><subject>Education</subject><subject>Exports</subject><subject>Gene Expression</subject><subject>Genes, Reporter</subject><subject>Hematology</subject><subject>Hepatitis</subject><subject>HIV</subject><subject>HIV-1 - physiology</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immunoprecipitation</subject><subject>Infectious diseases</subject><subject>Laboratories</subject><subject>Medicine</subject><subject>Microscopy</subject><subject>Nuclei</subject><subject>Nuclei (cytology)</subject><subject>Protein Binding</subject><subject>Proteins</subject><subject>Replication</subject><subject>Response Elements</subject><subject>rev Gene Products, Human Immunodeficiency Virus - metabolism</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA helicase</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Tropical diseases</subject><subject>Virology</subject><subject>Virus Replication</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNptUl1rFDEUDaLYuvoPRAd88WXWm9x8zYtQWrULBUFUfAvZTFJnyU7WZKbgv3fGnZZWfErIPefcc8Ih5CWFNUVF3-3SmHsb14fU-zWAFMDhETmlDbJaMsDH9-4n5FkpOwCBWsqn5ISh4pTz5pScXVz8EFWwrovdYAdfqsvN95pW2R9i5-zQpb6ypbKV8zGO0ebKpXqCDylXKVRf_M1z8iTYWPyL5VyRbx8_fD2_rK8-f9qcn13VTjA51MxpTgVvA7KAEm1wSqOlQAMFCJpiaLlirXTOQStV04gtVxgaSTVsQxC4Iq-PuoeYilnSF0NRKGzEFG1CbI6INtmdOeRub_Nvk2xn_j6kfG1sHjoXvZESdaOg1XwLXId221JEDYEpKYFN_lbk_bJt3O5963w_ZBsfiD6c9N1Pc51uDErZMIBJ4O0ikNOv0ZfB7Lsyf6LtfRpn31I0WqGYd735B_r_dPyIcjmVkn24M0PBzI24ZZm5EWZpxER7dT_IHem2AvgHKcWwsg</recordid><startdate>20130531</startdate><enddate>20130531</enddate><creator>Zhou, Xiuxia</creator><creator>Luo, Juan</creator><creator>Mills, Lisa</creator><creator>Wu, Shuangxin</creator><creator>Pan, Ting</creator><creator>Geng, Guannan</creator><creator>Zhang, Jim</creator><creator>Luo, Haihua</creator><creator>Liu, Chao</creator><creator>Zhang, Hui</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130531</creationdate><title>DDX5 facilitates HIV-1 replication as a cellular co-factor of Rev</title><author>Zhou, Xiuxia ; Luo, Juan ; Mills, Lisa ; Wu, Shuangxin ; Pan, Ting ; Geng, Guannan ; Zhang, Jim ; Luo, Haihua ; Liu, Chao ; Zhang, Hui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-2c84154df32f363afc783a101f100f813fd472d6ccc0d67995b473f96180bff53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Active Transport, Cell Nucleus</topic><topic>Antiviral agents</topic><topic>Biology</topic><topic>Biosynthesis</topic><topic>Cell Line</topic><topic>Confocal microscopy</topic><topic>Cytoplasm</topic><topic>DEAD-box RNA Helicases - genetics</topic><topic>DEAD-box RNA Helicases - metabolism</topic><topic>Deoxyribonucleic acid</topic><topic>Disease control</topic><topic>DNA</topic><topic>DNA helicase</topic><topic>Education</topic><topic>Exports</topic><topic>Gene Expression</topic><topic>Genes, Reporter</topic><topic>Hematology</topic><topic>Hepatitis</topic><topic>HIV</topic><topic>HIV-1 - physiology</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immunoprecipitation</topic><topic>Infectious diseases</topic><topic>Laboratories</topic><topic>Medicine</topic><topic>Microscopy</topic><topic>Nuclei</topic><topic>Nuclei (cytology)</topic><topic>Protein Binding</topic><topic>Proteins</topic><topic>Replication</topic><topic>Response Elements</topic><topic>rev Gene Products, Human Immunodeficiency Virus - metabolism</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA helicase</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Tropical diseases</topic><topic>Virology</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Xiuxia</creatorcontrib><creatorcontrib>Luo, Juan</creatorcontrib><creatorcontrib>Mills, Lisa</creatorcontrib><creatorcontrib>Wu, Shuangxin</creatorcontrib><creatorcontrib>Pan, Ting</creatorcontrib><creatorcontrib>Geng, Guannan</creatorcontrib><creatorcontrib>Zhang, Jim</creatorcontrib><creatorcontrib>Luo, Haihua</creatorcontrib><creatorcontrib>Liu, Chao</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Recent studies have shown that DDX1 and DDX3 are co-factors of Rev for the export of HIV-1 transcripts. In this report, we have demonstrated that DDX5 (p68), which is a multifunctional DEAD-box RNA helicase, functions as a new cellular co-factor of HIV-1 Rev. We found that DDX5 affects Rev function through the Rev-RRE axis and subsequently enhances HIV-1 replication. Confocal microscopy and co-immunoprecipitation analysis indicated that DDX5 binds to Rev and this interaction is largely dependent on RNA. If the DEAD-box motif of DDX5 is mutated, DDX5 loses almost all of its ability to bind to Rev, indicating that the DEAD-box motif of DDX5 is required for the interaction between DDX5 and Rev. Our data indicate that interference of DDX5-Rev interaction could reduce HIV-1 replication and potentially provide a new molecular target for anti-HIV-1 therapeutics.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23741449</pmid><doi>10.1371/journal.pone.0065040</doi><oa>free_for_read</oa></addata></record> |
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subjects | Active Transport, Cell Nucleus Antiviral agents Biology Biosynthesis Cell Line Confocal microscopy Cytoplasm DEAD-box RNA Helicases - genetics DEAD-box RNA Helicases - metabolism Deoxyribonucleic acid Disease control DNA DNA helicase Education Exports Gene Expression Genes, Reporter Hematology Hepatitis HIV HIV-1 - physiology Human immunodeficiency virus Humans Immunoprecipitation Infectious diseases Laboratories Medicine Microscopy Nuclei Nuclei (cytology) Protein Binding Proteins Replication Response Elements rev Gene Products, Human Immunodeficiency Virus - metabolism Ribonucleic acid RNA RNA helicase RNA, Messenger - genetics RNA, Messenger - metabolism Tropical diseases Virology Virus Replication |
title | DDX5 facilitates HIV-1 replication as a cellular co-factor of Rev |
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