EZH2 phosphorylation regulates Tat-induced HIV-1 transactivation via ROS/Akt signaling pathway

被引:18
|
作者
Zhang, Hong-Sheng [1 ]
Liu, Yang [1 ]
Wu, Tong-Chao [1 ]
Du, Guang-Yuan [1 ]
Zhang, Feng-Juan [1 ]
机构
[1] Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100124, Peoples R China
基金
北京市自然科学基金;
关键词
HIV-1; Enhancer of zeste homolog 2; Reactive oxygen species; AKT; REPEAT LTR TRANSACTIVATION; T-CELLS; TRANSCRIPTIONAL CONTROL; EPIGENETIC REGULATION; HISTONE MODIFICATIONS; DOWN-REGULATION; LATENCY; METHYLATION; CHROMATIN; THERAPY;
D O I
10.1016/j.febslet.2015.11.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
EZH2 plays a major role in HIV-1 latency, however, the molecular linkage between Tat-induced HIV-1 transactivation and EZH2 activity is not fully understood. It was shown Tat induced HIV-1 transactivation through inhibiting EZH2 activity. Tat decreased the levels of H3K27me3 and EZH2 occupy at the long terminal repeat (LTR) of HIV-1. We further showed for the first time that transfected with Tat construct resulted in an increase in phosphorylated EZH2 (p-EZH2), mediated by active Akt. ROS/Akt-dependent p-EZH2 was correlated with Tat-induced transactivation. Our study reveals that novel mechanisms allow Tat-induced HIV-1 transactivation by ROS/Akt-dependent downregulating the EZH2 epigenetic silencing machinery. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:4106 / 4111
页数:6
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