FKBP3 Induces Human Immunodeficiency Virus Type 1 Latency by Recruiting Histone Deacetylase 1/2 to the Viral Long Terminal Repeat

Author:

Yang Xinyi1,Zhao Xiaying1,Zhu Yuqi1,Shen Yinzhong2,Wang Yanan1,Lu Panpan1,Jiang Zhengtao1,Pan Hanyu1,Yang Jinlong1,Xun Jingna12,Zhao Lin1,Wang Jing1,Liang Zhiming1,Shen Xiaoting1,Liang Yue1,Lin Qinru1,Liang Huitong1,Jin Lu1,Zhang Dengji1,Liu Jun1,Wang Bin1,Jiang Shibo2,Xu Jianqing2,Wu Hao3,Lu Hongzhou2,Zhu Huanzhang1ORCID

Affiliation:

1. State Key Laboratory of Genetic Engineering and Engineering Research Center of Gene Technology, Ministry of Education, Institute of Genetics, School of Life Sciences, Fudan University, Shanghai, China

2. Department of Infectious Disease, Key Laboratory of Medical Molecular Virology of Ministry of Education/Health, School of Basic Medical Sciences and Shanghai Public Health Clinical Center, Fudan University, Shanghai, China

3. Center for Infectious Diseases, Beijing You'an Hospital, Capital Medical University, Fengtai District, Beijing, China

Abstract

The primary reason why AIDS cannot be completely cured is the existence of a latent HIV-1 reservoir. Currently, the facts of HIV-1 latency, including its establishment and maintenance, are incomplete.

Funder

National Natural Science Foundation of China

National Grand Program on Key infectious Disease

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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