PEBP1 suppresses HIV transcription and induces latency by inactivating MAPK/NF-κB signaling

  • EMBO Rep. 2020 Nov 5;21(11):e49305. doi: 10.15252/embr.201949305.
Xinyi Yang  1 ,  Yanan Wang  1 ,  Panpan Lu  1 ,  Yinzhong Shen  2 ,  Xiaying Zhao  1 ,  Yuqi Zhu  1 ,  Zhengtao Jiang  1 ,  He Yang  1 ,  Hanyu Pan  1 ,  Lin Zhao  1 ,  Yangcheng Zhong  1 ,  Jing Wang  1 ,  Zhiming Liang  1 ,  Xiaoting Shen  1 ,  Daru Lu  1 ,  Shibo Jiang  2 ,  Jianqing Xu  2 ,  Hao Wu  3 ,  Hongzhou Lu  2 ,  Guochun Jiang  4 ,  Huanzhang Zhu  1
Affiliations
  • 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, Beijing, China.
  • 4. UNC HIV Cure Center, Institute of Global Health and Infectious Diseases & Department of Biochemistry and Biophysics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Abstract

The latent HIV-1 reservoir is a major barrier to viral eradication. However, our understanding of how HIV-1 establishes latency is incomplete. Here, by performing a genome-wide CRISPR-Cas9 knockout library screen, we identify phosphatidylethanolamine-binding protein 1 (PEBP1), also known as Raf kinase inhibitor protein (RKIP), as a novel gene inducing HIV latency. Depletion of PEBP1 leads to the reactivation of HIV-1 in multiple models of latency. Mechanistically, PEBP1 de-phosphorylates Raf1/ERK/IκB and IKK/IκB signaling pathways to sequestrate NF-κB in the cytoplasm, which transcriptionally inactivates HIV-1 to induce latency. Importantly, the induction of PEBP1 expression by the green tea compound epigallocatechin-3-gallate (EGCG) prevents latency reversal by inhibiting nuclear translocation of NF-κB, thereby suppressing HIV-1 transcription in primary CD4+ T cells isolated from patients receiving antiretroviral therapy (ART). These results suggest a critical role for PEBP1 in the regulation of upstream NF-κB signaling pathways governing HIV transcription. Targeting of this pathway could be an option to control HIV reservoirs in patients in the future.

Keywords
CRISPR-Cas9; HIV latency; NF-κB; PEBP1; genome-wide screening.
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