Park Soo-Yeon, Choi Hyo-Kyoung, Jo Seong-Ho, Seo JaeSung, Han Eun-Jeong, Choi Kyung-Chul, Jeong Jae-Wook, Choi Youngsok, Yoon Ho-Geun
Department of Biochemistry and Molecular Biology, Brain Korea 21 PLUS Project for Medical Sciences, Yonsei University College of Medicine, Seoul, Republic of Korea.
Department of Biomedical Sciences, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Biochim Biophys Acta. 2015 May;1853(5):1060-72. doi: 10.1016/j.bbamcr.2015.01.006. Epub 2015 Jan 17.
Programmed cell death 5 (PDCD5) plays a crucial role in TP53-mediated apoptosis, but the regulatory mechanism of PDCD5 itself during apoptosis remains obscure. We identified YY1-associated factor 2 (YAF2) as a novel PDCD5-interacting protein in a yeast two-hybrid screen for PDCD5-interacting proteins. We found that YY1-associated factor 2 (YAF2) binds to and increases PDCD5 stability by inhibiting the ubiquitin-dependent proteosomal degradation pathway. However, knocking-down of YAF2 diminishes the levels of PDCD5 protein but not the levels of PDCD5 mRNA. Upon genotoxic stress response, YAF2 promotes TP53 activation via association with PDCD5. Strikingly, YAF2 failed to promote TP53 activation in the deletion of PDCD5, whereas restoration of wild-type PDCD5WT efficiently reversed the ineffectiveness of YAF2 on TP53 activation. Conversely, PDCD5 efficiently overcame the knockdown effect of YAF2 on ET-induced TP53 activation. Finally, impaired apoptosis upon PDCD5 ablation was substantially rescued by restoration of PDCD5WT but not YAF2-interacting defective PDCD5E4D nor TP53-interacting defective PDCD5E16D mutant. Our findings uncovered an apoptotic signaling cascade linking YAF2, PDCD5, and TP53 during genotoxic stress responses.
程序性细胞死亡蛋白5(PDCD5)在TP53介导的细胞凋亡中起关键作用,但PDCD5自身在细胞凋亡过程中的调控机制仍不清楚。在针对与PDCD5相互作用蛋白的酵母双杂交筛选中,我们鉴定出YY1相关因子2(YAF2)是一种新的与PDCD5相互作用的蛋白。我们发现YY1相关因子2(YAF2)通过抑制泛素依赖性蛋白酶体降解途径与PDCD5结合并增加其稳定性。然而,敲低YAF2会降低PDCD5蛋白水平,但不会降低PDCD5 mRNA水平。在基因毒性应激反应中,YAF2通过与PDCD5结合促进TP53激活。令人惊讶的是,在缺失PDCD5的情况下,YAF2未能促进TP53激活,而野生型PDCD5WT的恢复有效地逆转了YAF2对TP53激活的无效性。相反,PDCD5有效地克服了YAF2对ET诱导的TP53激活的敲低作用。最后,通过恢复PDCD5WT可显著挽救PDCD5缺失导致的细胞凋亡受损,但YAF2相互作用缺陷的PDCD5E4D或TP53相互作用缺陷的PDCD5E16D突变体则不能。我们的研究结果揭示了在基因毒性应激反应中连接YAF2、PDCD5和TP53的细胞凋亡信号级联。