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H3K9 histone methyltransferase G9a-mediated transcriptional activation of p21open access

Authors
Oh, Si-TaekKim, Kee-BeomChae, Yun-CheolKang, Joo-YoungHahn, YoonsooSeo, Sang-Beom
Issue Date
Mar-2014
Publisher
ELSEVIER SCIENCE BV
Keywords
Apoptosis; Etoposide; G9a; p21; Transcription
Citation
FEBS LETTERS, v.588, no.5, pp 685 - 691
Pages
7
Journal Title
FEBS LETTERS
Volume
588
Number
5
Start Page
685
End Page
691
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/12407
DOI
10.1016/j.febslet.2014.01.039
ISSN
0014-5793
1873-3468
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. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
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