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pubmed-article:16819297pubmed:abstractTextThe transcription factor E2F1 coordinates cell cycle progression and induces apoptosis in response to DNA damage stress. Aside from DNA damage, the role of E2F1 in the endoplasmic reticulum (ER) stress signaling pathways is unclear. We found that E2F1-/- murine embryonic fibroblasts (MEFs) are resistant to apoptosis triggered by the ER stress inducer thapsigargin. In addition, E2F1 deficiency results in enhanced phosphorylation of eukaryotic translation initiation factor 2a (eIF2a). These results therefore indicate that E2F1 deficiency increases phosphorylation of eIF2a in response to ER stress triggered by thapsigargin, and suggest that the reduction in ER stress-induced apoptosis in E2F1-deficient cells is related to the high level of eIF2a phosphorylation.lld:pubmed
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pubmed-article:16819297pubmed:authorpubmed-author:KimSoo JungSJlld:pubmed
pubmed-article:16819297pubmed:authorpubmed-author:PaikSang GiSGlld:pubmed
pubmed-article:16819297pubmed:authorpubmed-author:KimDong...lld:pubmed
pubmed-article:16819297pubmed:authorpubmed-author:YeomYoung...lld:pubmed
pubmed-article:16819297pubmed:authorpubmed-author:ParkKyung...lld:pubmed
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pubmed-article:16819297pubmed:pagination356-9lld:pubmed
pubmed-article:16819297pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:16819297pubmed:year2006lld:pubmed
pubmed-article:16819297pubmed:articleTitleRole of E2F1 in endoplasmic reticulum stress signaling.lld:pubmed
pubmed-article:16819297pubmed:affiliationFunctional Genomics Research Center, Division of Molecular Therapeutics, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-333, Korea.lld:pubmed
pubmed-article:16819297pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16819297pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed