Gu Chenjian, Ming Lijun, Fang Yili, Liu Xuejing, Zhang Junqi, Zelinskyy Gennadiy, Deng Qiang, Liu Jing, Xie Youhua
Key Laboratory of Medical Molecular Virology (Ministry of Education/National Health Commission/Chinese Academy of Medical Sciences), Department of Microbiology and Parasitology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai 200032, China.
University Hospital Essen, Institute of Virology, Essen 45147, Germany.
Sci Bull (Beijing). 2020 Apr 15;65(7):573-586. doi: 10.1016/j.scib.2019.12.028. Epub 2020 Jan 3.
SAMHD1 (Sterile Alpha Motif and Histidine-aspartate Domain containing protein 1) has been documented as a host factor that restricts HIV-1 and some DNA viruses. In this work, we attempted to explore possible effects of SAMHD1 on exogenous DNA and show that SAMHD1 exerts a general inhibition on the expression of exogenous DNA in vitro and in mice. This inhibition is achieved through repressing transcription of exogenous DNA. Intriguingly, unlike SAMHD1's restriction of HIV-1, such restriction does not require the dNTPase or RNase activities, or T592 phosphorylation of SAMHD1. Mechanistically, SAMHD1 enhances the expression of interferon regulatory factor-1 (IRF1), while IRF1 upregulation was demonstrated to inhibit exogenous DNA expression in a similar fashion as SAMHD1. IFNλ1, whose induction has been associated with IRF1 activation, is dispensable for SAMHD1/IRF1-mediated restriction of exogenous DNA, and neither type I nor II interferons appear to be involved. We also demonstrate that SAMHD1/IRF1-mediated restriction can effectively inhibit hepatitis B virus (HBV) antigen expression and progeny virus production in mouse models. In conclusion, these data support restriction of exogenous DNA as a novel function of SAMHD1.
SAMHD1(含无菌α基序和组氨酸 - 天冬氨酸结构域蛋白1)已被证明是一种限制HIV - 1和某些DNA病毒的宿主因子。在本研究中,我们试图探索SAMHD1对外源DNA的可能影响,并表明SAMHD1在体外和小鼠体内对外源DNA的表达具有普遍抑制作用。这种抑制作用是通过抑制外源DNA的转录实现的。有趣的是,与SAMHD1对HIV - 1的限制不同,这种限制不需要SAMHD1的dNTPase或RNase活性,也不需要T592磷酸化。从机制上讲,SAMHD1增强了干扰素调节因子 - 1(IRF1)的表达,而IRF1的上调被证明以与SAMHD1类似的方式抑制外源DNA表达。IFNλ1的诱导与IRF1激活有关,对于SAMHD1/IRF1介导的外源DNA限制是可有可无的,并且I型和II型干扰素似乎都不参与其中。我们还证明,SAMHD1/IRF1介导的限制可以有效抑制小鼠模型中乙型肝炎病毒(HBV)抗原的表达和子代病毒的产生。总之,这些数据支持外源DNA限制是SAMHD1的一种新功能。