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Cited 36 time in webofscience Cited 36 time in scopus
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dc.contributor.authorKim, W-
dc.contributor.authorChakraborty, G-
dc.contributor.authorKim, S-
dc.contributor.authorShin, J-
dc.contributor.authorPark, CH-
dc.contributor.authorJeong, MW-
dc.contributor.authorBharatham, N-
dc.contributor.authorYoon, HS-
dc.contributor.authorKim, KT-
dc.date.accessioned2016-03-31T09:06:58Z-
dc.date.available2016-03-31T09:06:58Z-
dc.date.created2012-03-22-
dc.date.issued2012-02-17-
dc.identifier.issn0021-9258-
dc.identifier.other2012-OAK-0000025116-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/16659-
dc.description.abstractVRK1-mediated phosphorylation of histone H3 should be restricted in mitosis for consistent cell cycling, and defects in this process trigger cellular catastrophe. However, an interphasic regulator against VRK1 has not been actually investigated so far. Here, we show that the histone variant macrodomain-containing histone H2A1.2 functions as a suppressor against VRK1 during interphase. The level of macroH2A1.2 was markedly reduced in the mitotic phase, and the macroH2A1.2-mediated inhibition of histone H3 phosphorylation occurred mainly during interphase. We also found direct interaction and binding features between VRK1 and macroH2A1.2 by NMR spectroscopy. Hence, our findings might provide valuable insight into the underlying molecular mechanism regarding an epigenetic regulation of histone H3 during the cell cycle.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAmerican Society for Biochemistry and Molecular Biology-
dc.relation.isPartOfJOURNAL OF BIOLOGICAL CHEMISTRY-
dc.subjectVACCINIA-RELATED KINASE-1-
dc.subjectINACTIVE X-CHROMOSOME-
dc.subjectVARIANT MACROH2A-
dc.subjectPHOSPHORYLATION-
dc.subjectMITOSIS-
dc.subjectVACCINIA-RELATED-KINASE-1-
dc.subjectACCUMULATION-
dc.subjectPROGRESSION-
dc.subjectEXPRESSION-
dc.subjectNUCLEUS-
dc.titleMacro Histone H2A1.2 (MacroH2A1) Protein Suppresses Mitotic Kinase VRK1 during Interphase-
dc.typeArticle-
dc.contributor.college융합생명공학부-
dc.identifier.doi10.1074/JBC.M111.281709-
dc.author.googleKim, W-
dc.author.googleChakraborty, G-
dc.author.googleKim, S-
dc.author.googleShin, J-
dc.author.googlePark, CH-
dc.author.googleJeong, MW-
dc.author.googleBharatham, N-
dc.author.googleYoon, HS-
dc.author.googleKim, KT-
dc.relation.volume287-
dc.relation.issue8-
dc.relation.startpage5278-
dc.relation.lastpage5289-
dc.contributor.id10104775-
dc.relation.journalJOURNAL OF BIOLOGICAL CHEMISTRY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF BIOLOGICAL CHEMISTRY, v.287, no.8, pp.5278 - 5289-
dc.identifier.wosid000300638000010-
dc.date.tcdate2019-01-01-
dc.citation.endPage5289-
dc.citation.number8-
dc.citation.startPage5278-
dc.citation.titleJOURNAL OF BIOLOGICAL CHEMISTRY-
dc.citation.volume287-
dc.contributor.affiliatedAuthorKim, KT-
dc.identifier.scopusid2-s2.0-84863148743-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc26-
dc.description.scptc24*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusVACCINIA-RELATED KINASE-1-
dc.subject.keywordPlusINACTIVE X-CHROMOSOME-
dc.subject.keywordPlusVARIANT MACROH2A-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusMITOSIS-
dc.subject.keywordPlusVACCINIA-RELATED-KINASE-1-
dc.subject.keywordPlusACCUMULATION-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusNUCLEUS-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-

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김경태KIM, KYONG TAI
Dept of Life Sciences
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