4.8 Article

The Influenza A Virus Endoribonuclease PA-X Usurps Host mRNA Processing Machinery to Limit Host Gene Expression

期刊

CELL REPORTS
卷 27, 期 3, 页码 776-+

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2019.03.063

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资金

  1. Natalie V. Zucker award from Tufts University
  2. NIH [T32 AI007422, R01 AI137358, T32 GM007310]
  3. Canadian Institutes for Health Research grant [MOP-136817]
  4. Applied Mathematics Program of the US Department of Energy (DOE) Office of Advanced Scientific Computing Research [DE-AC02-05CH11231]

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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.

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