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dc.contributor.authorCarpenter, Susan
dc.contributor.authorAiello, Daniel
dc.contributor.authorAtianand, Maninjay K.
dc.contributor.authorRicci, Emiliano P.
dc.contributor.authorGandhi, Pallavi
dc.contributor.authorHall, Lisa L.
dc.contributor.authorByron, Meg
dc.contributor.authorMonks, Brian G.
dc.contributor.authorHenry-Bezy, Meabh
dc.contributor.authorLawrence, Jeanne B.
dc.contributor.authorO'Neill, Luke A. J.
dc.contributor.authorMoore, Melissa J.
dc.contributor.authorCaffrey, Daniel R.
dc.contributor.authorFitzgerald, Katherine A.
dc.date2022-08-11T08:09:15.000
dc.date.accessioned2022-08-23T16:24:04Z
dc.date.available2022-08-23T16:24:04Z
dc.date.issued2013-08-16
dc.date.submitted2014-04-14
dc.identifier.citation<p>Carpenter S, Aiello D, Atianand MK, Ricci EP, Gandhi P, Hall LL, Byron M, Monks B, Henry-Bezy M, Lawrence JB, O'Neill LA, Moore MJ, Caffrey DR, Fitzgerald KA. A long noncoding RNA mediates both activation and repression of immune response genes. Science. 2013 Aug 16;341(6147):789-92. doi:10.1126/science.1240925. <a href="http://dx.doi.org/10.1126/science.1240925" target="_blank"> Link to article on publisher's site</a></p>
dc.identifier.issn0036-8075 (Linking)
dc.identifier.doi10.1126/science.1240925
dc.identifier.pmid23907535
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36039
dc.description.abstractAn inducible program of inflammatory gene expression is central to antimicrobial defenses. This response is controlled by a collaboration involving signal-dependent activation of transcription factors, transcriptional co-regulators, and chromatin-modifying factors. We have identified a long noncoding RNA (lncRNA) that acts as a key regulator of this inflammatory response. Pattern recognition receptors such as the Toll-like receptors induce the expression of numerous lncRNAs. One of these, lincRNA-Cox2, mediates both the activation and repression of distinct classes of immune genes. Transcriptional repression of target genes is dependent on interactions of lincRNA-Cox2 with heterogeneous nuclear ribonucleoprotein A/B and A2/B1. Collectively, these studies unveil a central role of lincRNA-Cox2 as a broad-acting regulatory component of the circuit that controls the inflammatory response.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=23907535&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1126/science.1240925
dc.subjectAnimals
dc.subjectCell Line
dc.subjectCell Nucleus
dc.subjectCyclooxygenase 2
dc.subjectCytokines
dc.subjectCytosol
dc.subject*Gene Expression Regulation
dc.subjectHeterogeneous-Nuclear Ribonucleoproteins
dc.subjectImmunity, Innate
dc.subjectInflammation
dc.subjectMacrophage Activation
dc.subjectMacrophages
dc.subjectMice
dc.subjectModels, Immunological
dc.subjectRNA Interference
dc.subjectRNA, Long Noncoding
dc.subjectToll-Like Receptors
dc.subjectTranscription Factors
dc.subjectTranscription, Genetic
dc.subjectTranscriptional Activation
dc.subjectImmunity
dc.subjectImmunology and Infectious Disease
dc.subjectMolecular Genetics
dc.titleA long noncoding RNA mediates both activation and repression of immune response genes
dc.typeJournal Article
dc.source.journaltitleScience (New York, N.Y.)
dc.source.volume341
dc.source.issue6147
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/lawrence/13
dc.identifier.contextkey5476826
html.description.abstract<p>An inducible program of inflammatory gene expression is central to antimicrobial defenses. This response is controlled by a collaboration involving signal-dependent activation of transcription factors, transcriptional co-regulators, and chromatin-modifying factors. We have identified a long noncoding RNA (lncRNA) that acts as a key regulator of this inflammatory response. Pattern recognition receptors such as the Toll-like receptors induce the expression of numerous lncRNAs. One of these, lincRNA-Cox2, mediates both the activation and repression of distinct classes of immune genes. Transcriptional repression of target genes is dependent on interactions of lincRNA-Cox2 with heterogeneous nuclear ribonucleoprotein A/B and A2/B1. Collectively, these studies unveil a central role of lincRNA-Cox2 as a broad-acting regulatory component of the circuit that controls the inflammatory response.</p>
dc.identifier.submissionpathlawrence/13
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentDepartment of Cell and Developmental Biology
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.source.pages789-92


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