Related Experiment Video
Updated: May 3, 2026

Combining Analysis of DNA in a Crude Virion Extraction with the Analysis of RNA from Infected Leaves to Discover New Virus Genomes
Published on: July 27, 2018
siRNA screen of early poxvirus genes identifies the AAA+ ATPase D5 as the virus genome-uncoating factor
Samuel Kilcher1, Florian Ingo Schmidt1, Christoph Schneider2
1Institute of Biochemistry, ETH Zurich, 8093 Zurich, Switzerland.
Abstract:
Poxvirus genome uncoating is a two-step process. First, cytoplasmic viral cores are activated and early viral genes are expressed. Next, cores are disassembled and the genomes released. This second step depends on an early viral factor(s) that has eluded identification for over 40 years. We used a large-scale, high-throughput RNAi screen directed against vaccinia virus (VACV) to identify the VACV AAA+ ATPase D5 as the poxvirus uncoating factor. We show that the ATPase activity of D5 is required for uncoating. Superresolution microscopy suggests that D5 acts directly at viral cores for genome release. Thus, the putative helicase D5 is a multifunctional protein required for genome uncoating and replication. Additionally, in vivo delivery of anti-D5 siRNAs reduced virus production in a mouse model of VACV infection. These results demonstrate the use of virus-targeting RNAi libraries to investigate viral gene function and suggest therapeutic avenues.
More Related Videos
Related Concept Videos
Leaky Scanning
Subviral Agents
Viruses of Archaea
Viruses with RNA Genomes

