Cancer-upregulated gene 2 (CUG2), a new component of centromere complex, is required for kinetochore function

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dc.contributor.authorKim, Hyejinko
dc.contributor.authorLee, Miaeko
dc.contributor.authorLee, Sunheeko
dc.contributor.authorPark, Byoungwooko
dc.contributor.authorKoh, Wansooko
dc.contributor.authorLee, Dong Junko
dc.contributor.authorLim, Dae-Sikko
dc.contributor.authorLee, Soojinko
dc.date.accessioned2013-03-08T15:32:52Z-
dc.date.available2013-03-08T15:32:52Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2009-06-
dc.identifier.citationMOLECULES AND CELLS, v.27, no.6, pp.697 - 701-
dc.identifier.issn1016-8478-
dc.identifier.urihttp://hdl.handle.net/10203/93427-
dc.description.abstractWe previously identified cancer-upregulated gene 2 (CUG2) as a commonly up-regulated gene in various human cancer tissues, especially in ovary, liver, and lung (Lee et al., 2007a). CUG2 was determined to be a nuclear protein that exhibited high proto-oncogenic activities when overexpressed in NIH3T3 mouse fibroblast cells. To identify other cellular functions of CUG2, we performed yeast two-hybrid screening and identified CENP-T, a component of CENP-A nucleosome complex in the centromere, as an interacting partner of CUG2. Moreover, CENP-A, the principle centromeric determinant, was also found in complex with CENP-T/CUG2. Immunofluorescent staining revealed the co-localization of CUG2 with human centromeric markers. Inhibition of CUG2 expression drastically affected cell viability by inducing aberrant cell division. We propose that CUG2 is a new component of the human centromeric complex that is required for proper chromosome segregation during mitosis.-
dc.languageEnglish-
dc.publisherKorean Soc Molecular & Cellular Biology-
dc.subjectCHROMATIN-
dc.subjectORGANIZATION-
dc.titleCancer-upregulated gene 2 (CUG2), a new component of centromere complex, is required for kinetochore function-
dc.typeArticle-
dc.identifier.wosid000267663600012-
dc.identifier.scopusid2-s2.0-67650299735-
dc.type.rimsART-
dc.citation.volume27-
dc.citation.issue6-
dc.citation.beginningpage697-
dc.citation.endingpage701-
dc.citation.publicationnameMOLECULES AND CELLS-
dc.identifier.doi10.1007/s10059-009-0083-2-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorLim, Dae-Sik-
dc.contributor.nonIdAuthorKim, Hyejin-
dc.contributor.nonIdAuthorLee, Miae-
dc.contributor.nonIdAuthorLee, Sunhee-
dc.contributor.nonIdAuthorPark, Byoungwoo-
dc.contributor.nonIdAuthorKoh, Wansoo-
dc.contributor.nonIdAuthorLee, Soojin-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcancer-upregulated gene 2-
dc.subject.keywordAuthorCENP-A-
dc.subject.keywordAuthorCENP-T-
dc.subject.keywordAuthorcentromere-
dc.subject.keywordAuthorkinetochore-
dc.subject.keywordPlusCHROMATIN-
dc.subject.keywordPlusORGANIZATION-
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