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SUMOylation of pontin chromatin-remodeling complex reveals a signal integration code in prostate cancer cells

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dc.contributor.authorKim, Jung Hwa-
dc.contributor.authorLee, A. Min-
dc.contributor.authorNam, Hye Jin-
dc.contributor.authorChoi, Hee June-
dc.contributor.authorYang, Jung Woo-
dc.contributor.authorLee, Jason S.-
dc.contributor.authorKim, Mi Hyang-
dc.contributor.authorKim, Su-Il-
dc.contributor.authorChung, Chin Ha-
dc.contributor.authorKim, Keun Il-
dc.contributor.authorBaek, Sung Hee-
dc.date.available2021-02-22T15:01:27Z-
dc.date.issued2007-12-
dc.identifier.issn0027-8424-
dc.identifier.issn1091-6490-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/14591-
dc.description.abstractPosttranslational modification by small ubiquitin-like modifier (SUMO) controls diverse cellular functions of transcription factors and coregulators and participates in various cellular processes including signal transduction and transcriptional regulation. Here, we report that pontin, a component of chromatin-remodeling complexes, is SUMO-modified, and that SUMOylation of pontin is an active control mechanism for the transcriptional regulation of pontin on androgen-receptor target genes in prostate cancer cells. Biochemical purification of pontin-containing complexes revealed the presence of the Ubc9 SUIVIO-conjugating enzyme that underlies its function as an activator. Intriguingly, 5 alpha-dihydroxytestosterone treatments significantly increased the SUMOylation of pontin, and SUMOylated pontin showed further activation of a subset of nuclear receptor-dependent transcription and led to an increase in proliferation and growth of prostate cancer cells. These data clearly define a functional model and provide a link between SUMO modification and prostate cancer progression.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherNATL ACAD SCIENCES-
dc.titleSUMOylation of pontin chromatin-remodeling complex reveals a signal integration code in prostate cancer cells-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1073/pnas.0710343105-
dc.identifier.scopusid2-s2.0-38049181050-
dc.identifier.wosid000252077400033-
dc.identifier.bibliographicCitationPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, v.104, no.52, pp 20793 - 20798-
dc.citation.titlePROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-
dc.citation.volume104-
dc.citation.number52-
dc.citation.startPage20793-
dc.citation.endPage20798-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusANDROGEN-RECEPTOR-
dc.subject.keywordPlusSTRUCTURAL BASIS-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusSUMO-
dc.subject.keywordPlusUBIQUITIN-
dc.subject.keywordPlusREPRESSION-
dc.subject.keywordPlusPREVENTS-
dc.subject.keywordPlusREPTIN-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusCHAINS-
dc.subject.keywordAuthorandrogen receptor-
dc.subject.keywordAuthorSUMO-
dc.subject.keywordAuthorUbc9-
dc.subject.keywordAuthortranscription-
dc.subject.keywordAuthorproliferation-
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