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Cited 62 time in webofscience Cited 64 time in scopus
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dc.contributor.authorKim, YK-
dc.contributor.authorHahm, B-
dc.contributor.authorJang, SK-
dc.date.accessioned2016-03-31T13:24:39Z-
dc.date.available2016-03-31T13:24:39Z-
dc.date.created2009-08-19-
dc.date.issued2000-11-24-
dc.identifier.issn0022-2836-
dc.identifier.other2000-OAK-0000001676-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/19763-
dc.description.abstractTranslation initiation of human Bip mRNA is directed by an internal ribosomal entry site (IRES) located in the 5' non-translated region. No trans-acting factor possibly involved in this process has as of yet been identified. For the encephalomyocarditis virus and other picornaviruses, polypyrimidine tract-binding protein (PTB) has been found to enhance the translation through IRES elements, probably by interaction with the IRES structure. Here, we report that PTB specifically binds to the central region (nt 50-117) of the Bip 5' non-translated region. Addition of purified PTB to rabbit reticulocyte lysate and overexpression of PTB in Cos-7 cells selectively inhibited Bip IRES-dependent translation On the other hand, depletion of endogenous PTB or addition of an RNA interacting with PTB enhanced the translational initiation directed by Bip IRES. These suggest that PTB can either enhance or inhibit IRES-dependent translation depending on mRNAs. (C) 2000 Academic Press.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherACADEMIC PRESS LTD-
dc.relation.isPartOfJOURNAL OF MOLECULAR BIOLOGY-
dc.subjecttranslation-
dc.subjectBip-
dc.subjectIRES-
dc.subjectPTB-
dc.subjectENCEPHALOMYOCARDITIS VIRUS-RNA-
dc.subjectRIBOSOME ENTRY SITE-
dc.subjectCAP-INDEPENDENT TRANSLATION-
dc.subject5&apos-
dc.subjectNONTRANSLATED REGION-
dc.subjectGLUCOSE-REGULATED PROTEINS-
dc.subjectHUMAN RHINOVIRUS RNA-
dc.subjectMOUTH-DISEASE VIRUS-
dc.subjectROUS-SARCOMA VIRUS-
dc.subjectMESSENGER-RNA-
dc.subjectINTERNAL INITIATION-
dc.titlePolypyrimidine tract-binding protein inhibits translation of Bip mRNA-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1006/jmbi.2000.4179-
dc.author.googleKim, YK-
dc.author.googleHahm, B-
dc.author.googleJang, SK-
dc.relation.volume304-
dc.relation.issue2-
dc.relation.startpage119-
dc.relation.lastpage133-
dc.contributor.id10088382-
dc.relation.journalJOURNAL OF MOLECULAR BIOLOGY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF MOLECULAR BIOLOGY, v.304, no.2, pp.119 - 133-
dc.identifier.wosid000165670100001-
dc.date.tcdate2019-01-01-
dc.citation.endPage133-
dc.citation.number2-
dc.citation.startPage119-
dc.citation.titleJOURNAL OF MOLECULAR BIOLOGY-
dc.citation.volume304-
dc.contributor.affiliatedAuthorJang, SK-
dc.identifier.scopusid2-s2.0-0034711379-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc59-
dc.type.docTypeArticle-
dc.subject.keywordPlusENCEPHALOMYOCARDITIS VIRUS-RNA-
dc.subject.keywordPlusRIBOSOME ENTRY SITE-
dc.subject.keywordPlusCAP-INDEPENDENT TRANSLATION-
dc.subject.keywordPlus5&apos-
dc.subject.keywordPlusNONTRANSLATED REGION-
dc.subject.keywordPlusGLUCOSE-REGULATED PROTEINS-
dc.subject.keywordPlusHUMAN RHINOVIRUS RNA-
dc.subject.keywordPlusMOUTH-DISEASE VIRUS-
dc.subject.keywordPlusROUS-SARCOMA VIRUS-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlusINTERNAL INITIATION-
dc.subject.keywordAuthortranslation-
dc.subject.keywordAuthorBip-
dc.subject.keywordAuthorIRES-
dc.subject.keywordAuthorPTB-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-

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Dept of Life Sciences
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