Graduate Program in Molecular Microbiology, Sackler School of Graduate Biomedical Sciences, Tufts University, Boston, MA, USA; Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA, USA.
Department of Microbiology & Immunology, Dalhousie University, Halifax, NS, Canada.
Cell Rep. 2019 Apr 16;27(3):776-792.e7. doi: 10.1016/j.celrep.2019.03.063.
Many viruses shut off host gene expression to inhibit antiviral responses. Viral proteins and host proteins required for viral replication are typically spared in this process, but the mechanisms of target selectivity during host shutoff remain poorly understood. Using transcriptome-wide and targeted reporter experiments, we demonstrate that the influenza A virus endoribonuclease PA-X usurps RNA splicing to selectively target host RNAs for destruction. Proximity-labeling proteomics reveals that PA-X interacts with cellular RNA processing proteins, some of which are partially required for host shutoff. Thus, PA-X taps into host nuclear pre-mRNA processing mechanisms to destroy nascent mRNAs shortly after their synthesis. This mechanism sets PA-X apart from other viral host shutoff proteins that target actively translating mRNAs in the cytoplasm. Our study reveals a unique mechanism of host shutoff that helps us understand how influenza viruses suppress host gene expression.
许多病毒会关闭宿主基因表达以抑制抗病毒反应。在这个过程中,通常会豁免病毒复制所需的病毒蛋白和宿主蛋白,但宿主关闭过程中的目标选择性机制仍知之甚少。通过转录组范围和靶向报告实验,我们证明甲型流感病毒内切核酸酶 PA-X 利用 RNA 剪接来选择性地靶向宿主 RNA 进行破坏。邻近标记蛋白质组学揭示,PA-X 与细胞 RNA 加工蛋白相互作用,其中一些蛋白部分参与宿主关闭。因此,PA-X 利用宿主核前体 mRNA 加工机制,在新生 mRNA 合成后不久将其破坏。这种机制使 PA-X 有别于其他靶向细胞质中正在翻译的 mRNA 的病毒宿主关闭蛋白。我们的研究揭示了一种宿主关闭的独特机制,帮助我们理解流感病毒如何抑制宿主基因表达。