The avengers: SAMHD1 cooperates with MX2/MxB to defend against HIV-1

Author:

Wan Zhi12,Zhong Gang3,Wang Huiqing1ORCID

Affiliation:

1. Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, China

2. Key Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, China

3. Department of Orthopedic Surgery, West China Hospital, Sichuan University/Trauma Center, West China Hospital, Sichuan University, Chengdu, China

Abstract

ABSTRACT SAMHD1 is an intrinsic limiting factor that effectively prevents HIV-1 infection in macrophages, dendritic cells, and resting CD4+ T cells. Extensive studies have underscored the indispensable role of the dNTPase activity of SAMHD1 in its antiviral function by primarily depleting dNTPs in quiescent cells, thereby impeding HIV-1 cDNA synthesis. However, recent advancements in understanding posttranslational modifications of SAMHD1 have revealed specific modification site mutants that maintain their ability to reduce dNTP levels while impairing the inhibition of HIV-1 replication. Thus, the precise anti-HIV-1 mechanism of SAMHD1 remains enigmatic, necessitating a comprehensive understanding of the underlying mechanisms to develop novel therapeutic strategies targeting its antiviral activity. Recent findings by Guo et al. shed light on the role of SAMHD1 as an HIV-1 core sensor in suppressing HIV-1 infection after viral cDNA synthesis through its interaction with MX2 (H. Guo, W. Yang, H. Li, J. Yang, et al., mBio 15:e01363-24, 2024, https://doi.org/10.1128/mbio.01363-24 ).

Funder

Science and technology department of Scichuan Province

National Key Research and Development Program of China

Sichuan University’s “0 to 1” innovation research program

Publisher

American Society for Microbiology

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