Suppr超能文献

PJA1 与 SMC5/6 复合物协作,以干扰素非依赖的方式限制 DNA 病毒和附加基因。

PJA1 Coordinates with the SMC5/6 Complex To Restrict DNA Viruses and Episomal Genes in an Interferon-Independent Manner.

机构信息

State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, China.

State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, China

出版信息

J Virol. 2018 Oct 29;92(22). doi: 10.1128/JVI.00825-18. Print 2018 Nov 15.

Abstract

Viral and episomal DNAs, as signs of infections and dangers, induce a series of immune responses in the host, and cells must sense foreign DNAs to eliminate the invaders. The cell nucleus is not "immune privileged" and exerts intrinsic mechanisms to control nuclear-replicating DNA viruses. Thus, it is important to understand the action of viral DNA sensing in the cell nucleus. Here, we reveal a mechanism of restriction of DNA viruses and episomal plasmids mediated by PJA1, a RING-H2 E3 ubiquitin ligase. PJA1 restricts the DNA viruses hepatitis B virus (HBV) and herpes simplex virus 1 (HSV-1) but not the RNA viruses enterovirus 71 (EV71) and vesicular stomatitis virus (VSV). Similarly, PJA1 inhibits episomal plasmids but not chromosome-integrated reporters or endogenous genes. In addition, PJA1 has no effect on endogenous type I and II interferons (IFNs) and interferon-stimulated genes (ISGs), suggesting that PJA1 silences DNA viruses independent of the IFN pathways. Interestingly, PJA1 interacts with the SMC5/6 complex (a complex essential for chromosome maintenance and HBV restriction) to facilitate the binding of the complex to viral and episomal DNAs in the cell nucleus. Moreover, treatment with inhibitors of DNA topoisomerases (Tops) and knockdown of Tops release PJA1-mediated silencing of viral and extrachromosomal DNAs. Taken together, results of this work demonstrate that PJA1 interacts with SMC5/6 and facilitates the complex to bind and eliminate viral and episomal DNAs through DNA Tops and thus reveal a distinct mechanism underlying restriction of DNA viruses and foreign genes in the cell nucleus. DNA viruses, including hepatitis B virus and herpes simplex virus, induce a series of immune responses in the host and lead to human public health concerns worldwide. In addition to cytokines in the cytoplasm, restriction of viral DNA in the nucleus is an important approach of host immunity. However, the mechanism of foreign DNA recognition and restriction in the cell nucleus is largely unknown. This work demonstrates that an important cellular factor (PJA1) suppresses DNA viruses and transfected plasmids independent of type I and II interferon (IFN) pathways. Instead, PJA1 interacts with the chromosome maintenance complex (SMC5/6), facilitates the complex to recognize and bind viral and episomal DNAs, and recruits DNA topoisomerases to restrict the foreign molecules. These results reveal a distinct mechanism underlying the silencing of viral and episomal invaders in the cell nuclei and suggest that PJA1 acts as a potential agent to prevent infectious and inflammatory diseases.

摘要

病毒和附加体 DNA 作为感染和危险的标志,会在宿主中引发一系列免疫反应,细胞必须感知外来 DNA 以清除入侵物。细胞核并非“免疫豁免”,它会发挥内在机制来控制核复制的 DNA 病毒。因此,了解细胞内病毒 DNA 感应的作用非常重要。在这里,我们揭示了 PJA1(一种 RING-H2 E3 泛素连接酶)介导的 DNA 病毒和附加体质粒限制的机制。PJA1 限制 DNA 病毒乙型肝炎病毒 (HBV) 和单纯疱疹病毒 1 (HSV-1),但不限制 RNA 病毒肠道病毒 71 (EV71) 和水疱性口炎病毒 (VSV)。同样,PJA1 抑制附加体质粒,但不抑制染色体整合报告基因或内源性基因。此外,PJA1 对内源性 I 型和 II 型干扰素 (IFN) 和干扰素刺激基因 (ISG) 没有影响,表明 PJA1 沉默 DNA 病毒与 IFN 途径无关。有趣的是,PJA1 与 SMC5/6 复合物(维持染色体和 HBV 限制所必需的复合物)相互作用,促进复合物在细胞核内与病毒和附加体 DNA 结合。此外,用 DNA 拓扑异构酶 (Tops) 抑制剂处理或敲低 Tops 会释放 PJA1 介导的对病毒和额外染色体 DNA 的沉默。总之,这项工作的结果表明,PJA1 与 SMC5/6 相互作用,并通过 DNA Tops 促进复合物结合并消除病毒和附加体 DNA,从而揭示了细胞核中 DNA 病毒和外源基因限制的独特机制。包括乙型肝炎病毒和单纯疱疹病毒在内的 DNA 病毒会在宿主中引发一系列免疫反应,导致全球公共卫生问题。除了细胞质中的细胞因子外,细胞核中病毒 DNA 的限制也是宿主免疫的重要途径。然而,细胞内外源 DNA 识别和限制的机制在很大程度上尚不清楚。这项工作表明,一种重要的细胞因子(PJA1)在不依赖 I 型和 II 型干扰素 (IFN) 途径的情况下抑制 DNA 病毒和转染质粒。相反,PJA1 与染色体维持复合物 (SMC5/6) 相互作用,促进复合物识别和结合病毒和附加体 DNA,并募集 DNA 拓扑异构酶来限制外来分子。这些结果揭示了细胞核中外来病毒和附加体入侵者沉默的独特机制,并表明 PJA1 可作为预防感染性和炎症性疾病的潜在药物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验