Hopping and Flipping of RNA Polymerase on DNA during Recycling for Reinitiation after Intrinsic Termination in Bacterial Transcription

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dc.contributor.authorKang, Wooyoungko
dc.contributor.authorHwang, Seunghako
dc.contributor.authorKang, Jin Youngko
dc.contributor.authorKang, Changwonko
dc.contributor.authorHohng, Sungchulko
dc.date.accessioned2021-03-23T01:10:36Z-
dc.date.available2021-03-23T01:10:36Z-
dc.date.created2021-03-22-
dc.date.created2021-03-22-
dc.date.created2021-03-22-
dc.date.created2021-03-22-
dc.date.created2021-03-22-
dc.date.created2021-03-22-
dc.date.issued2021-02-
dc.identifier.citationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.22, no.5, pp.1 - 13-
dc.identifier.issn1422-0067-
dc.identifier.urihttp://hdl.handle.net/10203/281768-
dc.description.abstractTwo different molecular mechanisms, sliding and hopping, are employed by DNA-binding proteins for their one-dimensional facilitated diffusion on nonspecific DNA regions until reaching their specific target sequences. While it has been controversial whether RNA polymerases (RNAPs) use one-dimensional diffusion in targeting their promoters for transcription initiation, two recent single-molecule studies discovered that post-terminational RNAPs use one-dimensional diffusion for their reinitiation on the same DNA molecules. Escherichia coli RNAP, after synthesizing and releasing product RNA at intrinsic termination, mostly remains bound on DNA and diffuses in both forward and backward directions for recycling, which facilitates reinitiation on nearby promoters. However, it has remained unsolved which mechanism of one-dimensional diffusion is employed by recycling RNAP between termination and reinitiation. Single-molecule fluorescence measurements in this study reveal that post-terminational RNAPs undergo hopping diffusion during recycling on DNA, as their one-dimensional diffusion coefficients increase with rising salt concentrations. We additionally find that reinitiation can occur on promoters positioned in sense and antisense orientations with comparable efficiencies, so reinitiation efficiency depends primarily on distance rather than direction of recycling diffusion. This additional finding confirms that orientation change or flipping of RNAP with respect to DNA efficiently occurs as expected from hopping diffusion.-
dc.languageEnglish-
dc.publisherMDPI-
dc.titleHopping and Flipping of RNA Polymerase on DNA during Recycling for Reinitiation after Intrinsic Termination in Bacterial Transcription-
dc.typeArticle-
dc.identifier.wosid000628297500001-
dc.identifier.scopusid2-s2.0-85101670001-
dc.type.rimsART-
dc.citation.volume22-
dc.citation.issue5-
dc.citation.beginningpage1-
dc.citation.endingpage13-
dc.citation.publicationnameINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.identifier.doi10.3390/ijms22052398-
dc.contributor.localauthorKang, Jin Young-
dc.contributor.localauthorKang, Changwon-
dc.contributor.nonIdAuthorKang, Wooyoung-
dc.contributor.nonIdAuthorHohng, Sungchul-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorCy3-
dc.subject.keywordAuthorCy5-
dc.subject.keywordAuthorEscherichia coli-
dc.subject.keywordAuthorfluorescent labeling-
dc.subject.keywordAuthorfluorescent transcription complex-
dc.subject.keywordAuthorone-dimensional facilitated diffusion-
dc.subject.keywordAuthorprotein-induced fluorescence enhancement-
dc.subject.keywordAuthorsingle-molecule fluorescence-
dc.subject.keywordAuthortranscription termination-
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CH-Journal Papers(저널논문)BS-Journal Papers(저널논문)
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