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ZNF219,一种新型转录抑制因子,通过与原型泡沫病毒的 LTR 启动子相互作用来抑制其转录。

ZNF219, a novel transcriptional repressor, inhibits transcription of the prototype foamy virus by interacting with the viral LTR promoter.

机构信息

Department of Immunology, School of Basic Medical Sciences, Hubei University of Medicine, Hubei Province, Shiyan 442000, China; Hubei Province Key Laboratory of Allergy and Immunology, Taikang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan 430071, China; Hubei Key Laboratory of Embryonic Stem Cell Research, Hubei University of Medicine, Hubei Province, Shiyan 442000, China.

Hubei Province Key Laboratory of Allergy and Immunology, Taikang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan 430071, China.

出版信息

Virus Res. 2023 Sep;334:199161. doi: 10.1016/j.virusres.2023.199161. Epub 2023 Jun 29.

Abstract

Prototype foamy virus (PFV) is an ancient retrovirus that infects humans with persistent latent infections and non-pathogenic consequences. Lifelong latent PFV infections can be caused by restrictive factors in the host. However, the molecular mechanisms underlying host cell regulation during PFV infection are not fully understood. The aim of the study was to investigate whether a zinc finger protein (ZFP), ZNF219, as a transcription factor, can regulate the transcriptional activity of the viral promoter. Here, using transcriptome sequencing, we found that ZNF219, is downregulated in PFV infected cells and that ZNF219 suppresses viral replication by targeting the viral 5'LTR promoter region to repress its transcription. We also found that PFV infection induced abnormal expression of miRNAs targeting the ZNF219-3'UTR to downregulate ZNF219 expression. These findings indicated that ZNF219 may be a potent antiviral factor for suppressing PFV infection, and may shed light on the mechanism of virus-host interactions.

摘要

原型泡沫病毒 (PFV) 是一种古老的逆转录病毒,它会导致人类持续性潜伏感染和非致病性后果。宿主中的限制因素会导致终身潜伏的 PFV 感染。然而,PFV 感染过程中宿主细胞调控的分子机制尚不完全清楚。本研究旨在探讨锌指蛋白 (ZFP) ZNF219 是否作为转录因子调节病毒启动子的转录活性。在这里,我们通过转录组测序发现,ZNF219 在 PFV 感染的细胞中下调,并且 ZNF219 通过靶向病毒 5'LTR 启动子区域来抑制其转录,从而抑制病毒复制。我们还发现,PFV 感染诱导针对 ZNF219-3'UTR 的 miRNAs 的异常表达,从而下调 ZNF219 的表达。这些发现表明,ZNF219 可能是一种有效的抗病毒因子,可抑制 PFV 感染,并可能为病毒-宿主相互作用的机制提供线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/295b/10410575/cced23061684/gr1.jpg

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