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dc.contributor.authorZapata, J.C.
dc.contributor.authorCampilongo, F.
dc.contributor.authorBarclay, R.A.
dc.date.accessioned2019-07-15T16:16:57Z
dc.date.available2019-07-15T16:16:57Z
dc.date.issued2017
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85015738153&doi=10.1016%2fj.virol.2017.03.002&partnerID=40&md5=0fa156591e96291d9ab2053079ef968a
dc.identifier.urihttp://hdl.handle.net/10713/10012
dc.description.abstractVarious epigenetic marks at the HIV-1 5’LTR suppress proviral expression and promote latency. Cellular antisense transcripts known as long noncoding RNAs (lncRNAs) recruit the polycomb repressor complex 2 (PRC2) to gene promoters, which catalyzes trimethylation of lysine 27 on histone H3 (H3K27me3), thus promoting nucleosome assembly and suppressing gene expression. We found that an HIV-1 antisense transcript expressed from the 3’LTR and encoding the antisense protein ASP promotes proviral latency. Expression of ASP RNA reduced HIV-1 replication in Jurkat cells. Moreover, ASP RNA expression promoted the establishment and maintenance of HIV-1 latency in Jurkat E4 cells. We show that this transcript interacts with and recruits PRC2 to the HIV-1 5’LTR, increasing accumulation of the suppressive epigenetic mark H3K27me3, while reducing RNA Polymerase II and thus proviral transcription. Altogether, our results suggest that the HIV-1 ASP transcript promotes epigenetic silencing of the HIV-1 5’LTR and proviral latency through the PRC2 pathway. Copyright 2017 The Authorsen_US
dc.description.urihttps://www.doi.org/10.1016/j.virol.2017.03.002en_US
dc.language.isoen_USen_US
dc.publisherAcademic Press Inc.en_US
dc.relation.ispartofVirology
dc.subjectAntisense transcripten_US
dc.subjectASPen_US
dc.subjectEpigenetic marksen_US
dc.subjectH3K27me3en_US
dc.subjectHIV-1en_US
dc.subjectPRC2en_US
dc.subjectViral latencyen_US
dc.titleThe Human Immunodeficiency Virus 1 ASP RNA promotes viral latency by recruiting the Polycomb Repressor Complex 2 and promoting nucleosome assemblyen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.virol.2017.03.002
dc.identifier.pmid28340355


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