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Nuclear TRADD prevents DNA damage-mediated death by facilitating non-homologous end-joining repair

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dc.contributor.authorKoo, GB-
dc.contributor.authorJi, JH-
dc.contributor.authorCho, H-
dc.contributor.authorMorgan, MJ-
dc.contributor.authorKim, YS-
dc.date.accessioned2018-08-24T01:49:03Z-
dc.date.available2018-08-24T01:49:03Z-
dc.date.issued2017-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/15936-
dc.description.abstractTNF receptor-associated death domain (TRADD) is an essential mediator of TNF receptor signaling, and serves as an adaptor to recruit other effectors. TRADD has been shown to cycle between the cytoplasm and nucleus due to its nuclear localization (NLS) and export sequences (NES). However, the underlying function of nuclear TRADD is poorly understood. Here we demonstrate that cytoplasmic TRADD translocates to DNA double-strand break sites (DSBs) during the DNA damage response (DDR). Deficiency of TRADD or its sequestration in cytosol leads to accumulation of gammaH2AX-positive foci in response to DNA damage, which is reversed by nuclear TRADD expression. TRADD facilitates non-homologous end-joining (NHEJ) by recruiting NHEJ repair factors 53BP1 and Ku70/80 complex, whereas TRADD is dispensable for homologous recombination (HR) repair. Finally, an impaired nuclear localization of TRADD triggers cell death through the persistent activation of JNK and accumulation of reactive oxygen species (ROS). Thus, our findings suggest that translocation of TRADD to DSBs into the nucleus contributes to cell survival in response to DNA damage through an activation of DNA damage repair.-
dc.language.isoen-
dc.titleNuclear TRADD prevents DNA damage-mediated death by facilitating non-homologous end-joining repair-
dc.typeArticle-
dc.identifier.pmid28611389-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469829/-
dc.contributor.affiliatedAuthor구, 기방-
dc.contributor.affiliatedAuthor지, 재훈-
dc.contributor.affiliatedAuthor조, 혜성-
dc.contributor.affiliatedAuthor김, 유선-
dc.type.localJournal Papers-
dc.identifier.doi10.1038/s41598-017-03211-z-
dc.citation.titleScientific reports-
dc.citation.volume7-
dc.citation.number1-
dc.citation.date2017-
dc.citation.startPage3332-
dc.citation.endPage3332-
dc.identifier.bibliographicCitationScientific reports, 7(1). : 3332-3332, 2017-
dc.identifier.eissn2045-2322-
dc.relation.journalidJ020452322-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Biochemistry & Molecular Biology
Journal Papers > Research Organization > Genomic Instability Research Center
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