X-Linked RNA-Binding Motif Protein Modulates HIV-1 Infection of CD4 + T Cells by Maintaining the Trimethylation of Histone H3 Lysine 9 at the Downstream Region of the 5′ Long Terminal Repeat of HIV Proviral DNA

Author:

Ma Li12,Jiang Qing-An12,Sun Li1,Yang Xianguang3,Huang Hai1,Jin Xia2,Zhang Chiyu2,Wang Jian-Hua24

Affiliation:

1. School of Life Science, Shanghai University, Shanghai, China

2. CAS Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, China

3. College of Life Science, Henan Normal University, Xinxiang, Henan Province, China

4. University of Chinese Academy of Sciences, Beijing, China

Abstract

HIV-1 latency featuring silence of transcription from HIV-1 proviral DNA represents a major obstacle for HIV-1 eradication. Reversible repression of HIV-1 5′-LTR-mediated transcription represents the main mechanism for HIV-1 to maintain latency. The 5′-LTR-driven HIV gene transcription can be modulated by multiple host factors and mechanisms. The hnRNPs are known to regulate gene expression. A member of the hnRNP family, RBMX, has been identified in this study as a novel HIV-1 restriction factor that modulates HIV-1 5′-LTR-driven transcription of viral genome in CD4 + T cells and maintains viral latency. These findings provide a new understanding of how host factors modulate HIV-1 infection and latency and suggest a potential new target for the development of HIV-1 therapies.

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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