Inoue Yasumichi, Kawachi Shiori, Ohkubo Tsubasa, Nagasaka Mai, Ito Shogo, Fukuura Keishi, Itoh Yuka, Ohoka Nobumichi, Morishita Daisuke, Hayashi Hidetoshi
Department of Cell Signaling, Graduate School of Pharmaceutical Sciences, Nagoya City University, Japan.
Department of Innovative Therapeutics Sciences, Cooperative Major in Nanopharmaceutical Sciences, Graduate School of Pharmaceutical Sciences, Nagoya City University, Japan.
FEBS Lett. 2017 Nov;591(21):3682-3691. doi: 10.1002/1873-3468.12869. Epub 2017 Oct 11.
Activating transcription factor 4 (ATF4) is well known for its role in the endoplasmic reticulum (ER) stress response. ATF4 also transcriptionally induces multiple effectors that determine cell fate depending on cellular context. In addition, ATF4 can communicate both pro-apoptotic and pro-survival signals. How ATF4 mediates its prosurvival roles, however, requires further investigation. Here, we report that the CDK inhibitor p21 is a novel target gene of ATF4. We identified two ATF4-responsive elements, one of which directly binds ATF4, within the first intron of the p21 gene. Importantly, overexpression of p21 enhances cell survival following ER stress induction, while p21 knockdown increases cell death. These results suggest that p21 induction plays a vital role in the cellular response to ER stress and indicate that p21 is a prosurvival effector of ATF4.
活化转录因子4(ATF4)因其在内质网(ER)应激反应中的作用而广为人知。ATF4还可转录诱导多种效应因子,这些效应因子根据细胞环境决定细胞命运。此外,ATF4可以传递促凋亡和促生存信号。然而,ATF4如何介导其促生存作用,仍需进一步研究。在此,我们报告细胞周期蛋白依赖性激酶抑制剂p21是ATF4的一个新靶基因。我们在p21基因的第一个内含子中鉴定出两个ATF4反应元件,其中一个直接与ATF4结合。重要的是,p21的过表达可增强内质网应激诱导后的细胞存活,而p21的敲低则增加细胞死亡。这些结果表明,p21的诱导在细胞对内质网应激的反应中起关键作用,并表明p21是ATF4的一个促生存效应因子。