The Long Noncoding RNA HEAL Regulates HIV-1 Replication through Epigenetic Regulation of the HIV-1 Promoter

Author:

Chao Ti-Chun1,Zhang Qiong1,Li Zhonghan1,Tiwari Shashi Kant1,Qin Yue1,Yau Edwin1,Sanchez Ana2,Singh Gatikrushna1,Chang Kungyen1,Kaul Marcus23,Karris Maile Ann Young4,Rana Tariq M.1

Affiliation:

1. Division of Genetics, Department of Pediatrics, UCSD Center for AIDS Research, and Institute for Genomic Medicine, University of California San Diego, La Jolla, California, USA

2. Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California, USA

3. School of Medicine, Division of Biomedical Sciences, University of California, Riverside, California, USA

4. Division of Infectious Diseases, UCSD Center for AIDS Research, Department of Medicine, University of California San Diego, La Jolla, California, USA

Abstract

Despite our increased understanding of the functions of lncRNAs, their potential to develop HIV/AIDS cure strategies remains unexplored. A genome-wide analysis of lncRNAs in HIV-1-infected primary monocyte-derived macrophages (MDMs) was performed, and 1,145 differentially expressed lncRNAs were identified. An lncRNA named H IV-1- e nh a nced l ncRNA ( HEAL ) is upregulated by HIV-1 infection and promotes HIV replication in T cells and macrophages. HEAL forms a complex with the RNA-binding protein FUS to enhance transcriptional coactivator p300 recruitment to the HIV promoter. Furthermore, HEAL knockdown and knockout prevent HIV-1 recrudescence in T cells and microglia upon cessation of azidothymidine treatment, suggesting HEAL as a potential therapeutic target to cure HIV-1/AIDS.

Funder

HHS | National Institutes of Health

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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