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The RNA Exosome Syncs IAV-RNAPII Transcription to Promote Viral Ribogenesis and Infectivity
Author(s) -
Alexander Rialdi,
Judd F. Hultquist,
David JimenezMorales,
Zuleyma Peralta,
Laura Campisi,
Romain Fenouil,
Natasha Moshkina,
Zhen Zhen Wang,
Brice Laffleur,
Robyn M. Kaake,
Michael McGregor,
Kelsey M. Haas,
Evangelos Pefanis,
Randy A. Albrecht,
Lars Pache,
Sumit K. Chanda,
Joanna C. Jen,
Jordi Ochando,
Minji Byun,
Uttiya Basu,
Adolfo Garcı́a-Sastre,
Nevan J. Krogan,
Harm van Bakel,
Ivan Marazzi
Publication year - 2017
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2017.04.021
Subject(s) - biology , infectivity , transcription (linguistics) , exosome complex , virology , rna , exosome , microbiology and biotechnology , genetics , rna processing , virus , gene , microrna , microvesicles , philosophy , linguistics
The nuclear RNA exosome is an essential multi-subunit complex that controls RNA homeostasis. Congenital mutations in RNA exosome genes are associated with neurodegenerative diseases. Little is known about the role of the RNA exosome in the cellular response to pathogens. Here, using NGS and human and mouse genetics, we show that influenza A virus (IAV) ribogenesis and growth are suppressed by impaired RNA exosome activity. Mechanistically, the nuclear RNA exosome coordinates the initial steps of viral transcription with RNAPII at host promoters. The viral polymerase complex co-opts the nuclear RNA exosome complex and cellular RNAs en route to 3' end degradation. Exosome deficiency uncouples chromatin targeting of the viral polymerase complex and the formation of cellular:viral RNA hybrids, which are essential RNA intermediates that license transcription of antisense genomic viral RNAs. Our results suggest that evolutionary arms races have shaped the cellular RNA quality control machinery.

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