| Literature DB >> 24492005 |
Si-Taek Oh1, Kee-Beom Kim1, Yun-Cheol Chae1, Joo-Young Kang1, Yoonsoo Hahn2, Sang-Beom Seo3.
Abstract
We report that H3K9 HMTase G9a activates transcription of the cell cycle regulatory gene, p21, in p53-null H1299 cells. Positive regulation of p21 by G9a is independent of its HMTase activity. We demonstrate that G9a upregulates p21 via interaction with PCAF, and provide evidence that the activating complex is recruited to the p21 promoter upon DNA damage-inducing agent etoposide treatment. Our study suggests that G9a decreases proliferation and cell viability by increasing the level of p21-mediated apoptosis. Our results suggest that G9a functions as a coactivator for p21 transcription, and directs cells to undergo apoptosis.Entities:
Keywords: Apoptosis; Etoposide; G9a; Transcription; p21
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Year: 2014 PMID: 24492005 DOI: 10.1016/j.febslet.2014.01.039
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124