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Effects of the BH3-only protein human Noxa on mitochondrial dynamics.

DC Field Value Language
dc.contributor.authorWoo, HN-
dc.contributor.authorSeo, YW-
dc.contributor.authorMoon, AR-
dc.contributor.authorJeong, SY-
dc.contributor.authorChoi, EK-
dc.contributor.authorKim, TH-
dc.date.accessioned2010-11-26T05:15:04Z-
dc.date.available2010-11-26T05:15:04Z-
dc.date.issued2009-
dc.identifier.issn0014-5793-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/321-
dc.description.abstractMitochondria form reticular networks comprised of filamentous tubules and continuously move and change shape. Bcl-2 family proteins actively participate in the regulation of mitochondria fragmentation. Here, we show that human Noxa, which belongs to the BH3-only pro-apoptotic Bcl-2 family, causes mitochondrial fragmentation. We found that while the Bcl-2 homology 3 (BH3) domain of Noxa is not associated with mitochondrial fragmentation, the mitochondrial targeting domain (MTD) of Noxa is the region responsible for inducing fragmentation. Two leucine residues in MTD play a key role in the process. Furthermore, the lack of Noxa causes a significant reduction of Velcade-induced mitochondrial fragmentation. Together, these results provide novel insight into the role of Noxa in mitochondrial dynamics and cell death.-
dc.formattext/plain-
dc.language.isoen-
dc.subject.MESHAmino Acid Sequence-
dc.subject.MESHAnimals-
dc.subject.MESHBoronic Acids-
dc.subject.MESHCell Death-
dc.subject.MESHHela Cells-
dc.subject.MESHHumans-
dc.subject.MESHLeucine-
dc.subject.MESHMitochondria-
dc.subject.MESHMolecular Sequence Data-
dc.subject.MESHProtease Inhibitors-
dc.subject.MESHProto-Oncogene Proteins c-bcl-2-
dc.subject.MESHPyrazines-
dc.subject.MESHSignal Transduction-
dc.subject.MESHbcl-2-Associated X Protein-
dc.titleEffects of the BH3-only protein human Noxa on mitochondrial dynamics.-
dc.typeArticle-
dc.identifier.pmid19540835-
dc.identifier.urlhttp://linkinghub.elsevier.com/retrieve/pii/S0014-5793(09)00475-X-
dc.contributor.affiliatedAuthor정, 선용-
dc.type.localJournal Papers-
dc.identifier.doi10.1016/j.febslet.2009.06.029-
dc.citation.titleFEBS letters-
dc.citation.volume583-
dc.citation.number14-
dc.citation.date2009-
dc.citation.startPage2349-
dc.citation.endPage2354-
dc.identifier.bibliographicCitationFEBS letters, 583(14). : 2349-2354, 2009-
dc.identifier.eissn1873-3468-
dc.relation.journalidJ000145793-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Medical Genetics
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