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NM23-H2 involves in negative regulation of Diva and Bcl2L10 in apoptosis signaling

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dc.contributor.authorKang, Yeongsup-
dc.contributor.authorLee, Deug-Chan-
dc.contributor.authorHan, Jiyou-
dc.contributor.authorYoon, Seongmin-
dc.contributor.authorWon, Miae-
dc.contributor.authorYeom, Ji-Hyun-
dc.contributor.authorSeong, Maeng-Je-
dc.contributor.authorKo, Jeong-Jae-
dc.contributor.authorLee, Kyung-Ah-
dc.contributor.authorLee, Kangseok-
dc.contributor.authorBae, Jeehyeon-
dc.date.available2019-05-30T05:42:45Z-
dc.date.issued2007-07-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24031-
dc.description.abstractThe Bcl-2 family members are evolutionally conserved and crucial regulators of apoptosis. Diva (Boo), an ortholog of Bcl2L10 or Bcl-B, is a member of the Bcl-2 family that has contradictory functions in apoptosis. To understand the signaling mechanisms of Diva, we searched for proteins that interact with Diva using the yeast two-hybrid system. We identified a nucleoside diphosphate kinase isoform, NM23-H2. Here, we show that Diva bound to NM23-H2 in cells in which the transmembrane domain of Diva was required, and both proteins were colocalized in cytoplasm. Of interest, Diva protein level was significantly down-regulated by NM23-H2 as knock down of NM23-H2 restored Diva expression. Overexpression of NM23-H2 induced apoptosis, and the depletion of NM23-H2 led to the increase of Diva's apoptotic activity. Thus, these results indicate the existence of a previously undiscovered mechanism by which NM23-H2 involves in the regulation of Diva-mediated apoptosis. (C) 2007 Elsevier Inc. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleNM23-H2 involves in negative regulation of Diva and Bcl2L10 in apoptosis signaling-
dc.typeArticle-
dc.identifier.doi10.1016/j.bbrc.2007.05.090-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.359, no.1, pp 76 - 82-
dc.description.isOpenAccessN-
dc.identifier.wosid000247257600013-
dc.identifier.scopusid2-s2.0-34249725600-
dc.citation.endPage82-
dc.citation.number1-
dc.citation.startPage76-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume359-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorDiva-
dc.subject.keywordAuthorBcl2L10-
dc.subject.keywordAuthorBoo-
dc.subject.keywordAuthorBcl-B-
dc.subject.keywordAuthorNM23-H2-
dc.subject.keywordAuthorNME-
dc.subject.keywordAuthorapoptosis-
dc.subject.keywordPlusCELL-DEATH-
dc.subject.keywordPlusBCL-2 FAMILY-
dc.subject.keywordPlusKINASE-
dc.subject.keywordPlusINTERACTS-
dc.subject.keywordPlusAPAF-1-
dc.subject.keywordPlusMEMBER-
dc.subject.keywordPlusBINDS-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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