Effects of different target sites on antisense RNA-mediated regulation of gene expression

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dc.contributor.authorPark, Hong-Marnko
dc.contributor.authorYoon, Yeongseongko
dc.contributor.authorSuk, Shinaeko
dc.contributor.authorLee, Ji Youngko
dc.contributor.authorLee, Younghoonko
dc.date.accessioned2015-01-29T07:29:00Z-
dc.date.available2015-01-29T07:29:00Z-
dc.date.created2014-12-22-
dc.date.created2014-12-22-
dc.date.issued2014-11-
dc.identifier.citationBMB REPORTS, v.47, no.11, pp.619 - 624-
dc.identifier.issn1976-6696-
dc.identifier.urihttp://hdl.handle.net/10203/193911-
dc.description.abstractAntisense RNA is a type of noncoding RNA (ncRNA) that binds to complementary mRNA sequences and induces gene repression by inhibiting translation or degrading mRNA. Recently, several small ncRNAs (sRNAs) have been identified in Escherichia coli that act as antisense RNA mainly via base pairing with mRNA. The base pairing predominantly leads to gene repression, and in some cases, gene activation. In the current study, we examined how the location of target sites affects sRNA-mediated gene regulation. An efficient antisense RNA expression system was developed, and the effects of antisense RNAs on various target sites in a model mRNA were examined. The target sites of antisense RNAs suppressing gene expression were identified, not only in the translation initiation region (TIR) of mRNA, but also at the junction between the coding region and 3' untranslated region. Surprisingly, an antisense RNA recognizing the upstream region of TIR enhanced gene expression through increasing mRNA stability.-
dc.languageEnglish-
dc.publisherKOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY-
dc.subjectRATIONAL SIRNA DESIGN-
dc.subjectESCHERICHIA-COLI-
dc.subjectMESSENGER-RNA-
dc.subjectBINDING-
dc.subjectHFQ-
dc.subjectTRANSCRIPTION-
dc.subjectRECOGNITION-
dc.subjectPREDICTION-
dc.subjectSTABILITY-
dc.subjectBACTERIA-
dc.titleEffects of different target sites on antisense RNA-mediated regulation of gene expression-
dc.typeArticle-
dc.identifier.wosid000345347400003-
dc.identifier.scopusid2-s2.0-84914809939-
dc.type.rimsART-
dc.citation.volume47-
dc.citation.issue11-
dc.citation.beginningpage619-
dc.citation.endingpage624-
dc.citation.publicationnameBMB REPORTS-
dc.identifier.doi10.5483/BMBRep.2014.47.11.257-
dc.contributor.localauthorLee, Younghoon-
dc.contributor.nonIdAuthorYoon, Yeongseong-
dc.contributor.nonIdAuthorLee, Ji Young-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorArtificial RNA-
dc.subject.keywordAuthorAntisense RNA-
dc.subject.keywordAuthorDouble stem-loop-
dc.subject.keywordAuthorEnhancer-
dc.subject.keywordAuthorUp-regulation-
dc.subject.keywordPlusRATIONAL SIRNA DESIGN-
dc.subject.keywordPlusESCHERICHIA-COLI-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusHFQ-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordPlusPREDICTION-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusBACTERIA-
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CH-Journal Papers(저널논문)
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