Department of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 156-756, South Korea.
Department of Life Science, College of Natural Sciences, Chung-Ang University, Seoul 156-756, South Korea.
FEBS Lett. 2014 Mar 3;588(5):685-91. doi: 10.1016/j.febslet.2014.01.039. Epub 2014 Feb 1.
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.
我们报告称,H3K9 HMTase G9a 在 p53 缺失的 H1299 细胞中激活细胞周期调节基因 p21 的转录。G9a 对 p21 的正调控不依赖于其 HMTase 活性。我们证明 G9a 通过与 PCAF 的相互作用上调 p21,并提供证据表明激活复合物在 DNA 损伤诱导剂依托泊苷处理后被募集到 p21 启动子。我们的研究表明,G9a 通过增加 p21 介导的细胞凋亡水平来降低增殖和细胞活力。我们的结果表明,G9a 作为 p21 转录的共激活因子发挥作用,并指导细胞凋亡。