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Cited 125 time in webofscience Cited 126 time in scopus
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dc.contributor.authorBack, SH-
dc.contributor.authorKim, YK-
dc.contributor.authorKim, WJ-
dc.contributor.authorCho, S-
dc.contributor.authorOh, HR-
dc.contributor.authorKim, JE-
dc.contributor.authorJang, SK-
dc.date.accessioned2015-06-25T02:37:06Z-
dc.date.available2015-06-25T02:37:06Z-
dc.date.created2009-08-19-
dc.date.issued2002-03-
dc.identifier.issn0022-538X-
dc.identifier.other2015-OAK-0000002461en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/11308-
dc.description.abstractThe translation of polioviral mRNA occurs through an internal ribosomal entry site (IRES). Several RNA-binding proteins, such as polypyrimidine tract-binding protein (PTB) and poly (rC)-binding protein (PCBP), are required for the poliovirus IRES-dependent translation. Here we report that a poliovirus protein, 3C(pro) (and/or 3CD(pro)), cleaves PTB isoforms (PTB1, PTB2, and PTB4). Three 3C(pro) target sites (one major target site and two minor target sites) exist in PTBs. PTB fragments generated by poliovirus infection are redistributed to the cytoplasm from the nucleus, where most of the intact PTBs are localized. Moreover, these PTB fragments inhibit polioviral IRES-dependent translation in a cell-based assay system. We speculate that the proteolytic cleavage of PTBs may contribute to the molecular switching from translation to replication of polioviral RNA.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherAMER SOC MICROBIOLOGY-
dc.relation.isPartOfJOURNAL OF VIROLOGY-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleTranslation of polioviral mRNA is inhibited by cleavage of polypyrimidine tract-binding proteins executed by polioviral 3C(pro)-
dc.typeArticle-
dc.contributor.college생명과학과en_US
dc.identifier.doi10.1128/jvi.76.5.2529-2542.2002-
dc.author.googleBack, SHen_US
dc.author.googleKim, YKen_US
dc.author.googleJang, SKen_US
dc.author.googleKim, JEen_US
dc.author.googleOh, HRen_US
dc.author.googleCho, Sen_US
dc.author.googleKim, WJen_US
dc.relation.volume76en_US
dc.relation.issue5en_US
dc.relation.startpage2529en_US
dc.relation.lastpage2542en_US
dc.contributor.id10088382en_US
dc.relation.journalJOURNAL OF VIROLOGYen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF VIROLOGY, v.76, no.5, pp.2529 - 2542-
dc.identifier.wosid000173756300052-
dc.date.tcdate2019-01-01-
dc.citation.endPage2542-
dc.citation.number5-
dc.citation.startPage2529-
dc.citation.titleJOURNAL OF VIROLOGY-
dc.citation.volume76-
dc.contributor.affiliatedAuthorJang, SK-
dc.identifier.scopusid2-s2.0-0036168869-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc110-
dc.type.docTypeArticle-
dc.subject.keywordPlusINTERNAL RIBOSOMAL ENTRY-
dc.subject.keywordPlus5&apos-
dc.subject.keywordPlusNONTRANSLATED REGION-
dc.subject.keywordPlusENCEPHALOMYOCARDITIS VIRUS-RNA-
dc.subject.keywordPlusCAP-INDEPENDENT TRANSLATION-
dc.subject.keywordPlusENCODED PROTEASE 3C(PRO)-
dc.subject.keywordPlusMOUTH-DISEASE VIRUS-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlus5&apos-
dc.subject.keywordPlus-UNTRANSLATED REGION-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusPOLY(RC) BINDING-PROTEIN-2-
dc.relation.journalWebOfScienceCategoryVirology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaVirology-

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