Karasik Agnes, Guydosh Nicholas R
Laboratory of Biochemistry and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Wiley Interdiscip Rev RNA. 2024 Nov-Dec;15(6):e1878. doi: 10.1002/wrna.1878.
Ribonuclease L is an endonuclease that is activated as part of the dsRNA-driven innate immune response. Active RNase L cleaves pathogenic RNAs as a way to eliminate infections. However, there are additional and unexpected ways that RNase L causes changes in the host that promote an immune response and contribute to its role in host defense. Central to these unconventional mechanisms is the observation that RNase L also degrades the mRNA of the host. In turn, mRNA fragments that RNase L generates can be translated. This causes activation of a ribosome collision sensor that leads to downstream signaling and cell death. Additionally, the liberation of RNA binding proteins after RNA decay appears to affect gene expression. In this review, we discuss these and other recent advances that focus on novel and unusual ways RNase L contributes to innate immunity.
核糖核酸酶L是一种核酸内切酶,作为双链RNA驱动的先天免疫反应的一部分被激活。活性核糖核酸酶L切割致病RNA以消除感染。然而,核糖核酸酶L还有其他意想不到的方式导致宿主发生变化,从而促进免疫反应并有助于其在宿主防御中的作用。这些非常规机制的核心是观察到核糖核酸酶L也会降解宿主的mRNA。反过来,核糖核酸酶L产生的mRNA片段可以被翻译。这会激活核糖体碰撞传感器,导致下游信号传导和细胞死亡。此外,RNA衰变后RNA结合蛋白的释放似乎会影响基因表达。在这篇综述中,我们讨论了这些以及其他最近的进展,这些进展聚焦于核糖核酸酶L对先天免疫做出贡献的新颖和不同寻常的方式。