Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115, USA; email:
Program in Cellular and Molecular Medicine, Boston Children's Hospital, Boston, Massachusetts 02115, USA.
Annu Rev Immunol. 2019 Apr 26;37:349-375. doi: 10.1146/annurev-immunol-042718-041356. Epub 2019 Jan 23.
Detection of double-stranded RNAs (dsRNAs) is a central mechanism of innate immune defense in many organisms. We here discuss several families of dsRNA-binding proteins involved in mammalian antiviral innate immunity. These include RIG-I-like receptors, protein kinase R, oligoadenylate synthases, adenosine deaminases acting on RNA, RNA interference systems, and other proteins containing dsRNA-binding domains and helicase domains. Studies suggest that their functions are highly interdependent and that their interdependence could offer keys to understanding the complex regulatory mechanisms for cellular dsRNA homeostasis and antiviral immunity. This review aims to highlight their interconnectivity, as well as their commonalities and differences in their dsRNA recognition mechanisms.
双链 RNA(dsRNAs)的检测是许多生物体固有免疫防御的一个核心机制。我们在这里讨论了几种参与哺乳动物抗病毒固有免疫的 dsRNA 结合蛋白家族。这些包括 RIG-I 样受体、蛋白激酶 R、寡聚腺苷酸合成酶、作用于 RNA 的腺苷脱氨酶、RNA 干扰系统和其他含有 dsRNA 结合域和解旋酶域的蛋白质。研究表明,它们的功能高度相互依赖,它们的相互依赖性可能为理解细胞内 dsRNA 动态平衡和抗病毒免疫的复杂调控机制提供关键线索。本综述旨在强调它们的相互关联性,以及它们在 dsRNA 识别机制方面的共性和差异。