| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2040412 | Cell Reports | 2012 | 12 Pages |
SummaryA two-step, automated, high-throughput RNAi silencing screen was used to identify host cell factors required during vaccinia virus infection. Validation and analysis of clustered hits revealed previously unknown processes during virus entry, including a mechanism for genome uncoating. Viral core proteins were found to be already ubiquitinated during virus assembly. After entering the cytosol of an uninfected cell, the viral DNA was released from the core through the activity of the cell’s proteasomes. Next, a Cullin3-based ubiquitin ligase mediated a further round of ubiquitination and proteasome action. This was needed in order to initiate viral DNA replication. The results accentuate the value of large-scale RNAi screens in providing directions for detailed cell biological investigation of complex pathways. The list of cell functions required during poxvirus infection will, moreover, provide a resource for future virus-host cell interaction studies and for the discovery of antivirals.
Graphical AbstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► A 7,000 human gene RNAi screen identifies 188 factors required for poxvirus infection ► The ubiquitin/proteasome system is instrumental in viral genome uncoating ► Preubiquitinated core proteins drive DNA release from incoming virus ► A cullin-3 ubiquitin ligase complex is needed for initiation of DNA replication
