| Literature DB >> 31851912 |
Michael Bauer1, Justin W Flatt2, Daria Seiler3, Bettina Cardel3, Mario Emmenlauer4, Karin Boucke3, Maarit Suomalainen3, Silvio Hemmi3, Urs F Greber5.
Abstract
Adenoviruses (AdVs) cause respiratory, ocular, and gastrointestinal tract infection and inflammation in immunocompetent people and life-threatening disease upon immunosuppression. AdV vectors are widely used in gene therapy and vaccination. Incoming particles attach to nuclear pore complexes (NPCs) of post-mitotic cells, then rupture and deliver viral DNA (vDNA) to the nucleus or misdeliver to the cytosol. Our genome-wide RNAi screen in AdV-infected cells identified the RING-type E3 ubiquitin ligase Mind bomb 1 (Mib1) as a proviral host factor for AdV infection. Mib1 is implicated in Notch-Delta signaling, ciliary biogenesis, and RNA innate immunity. Mib1 depletion arrested incoming AdVs at NPCs. Induced expression of full-length but not ligase-defective Mib1 in knockout cells triggered vDNA uncoating from NPC-tethered virions, nuclear import, misdelivery of vDNA, and vDNA expression. Mib1 is an essential host factor for AdV uncoating in human cells, and it provides a new concept for licensing virion DNA delivery through the NPC.Entities:
Keywords: E3 ubiquitin ligase; cell biology; click chemistry; fluorescence microscopy; nuclear import; ubiquitin proteasome system; ubiquitination; uncoating; virology; virus entry
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Year: 2019 PMID: 31851912 DOI: 10.1016/j.celrep.2019.11.064
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423