| Literature DB >> 29290611 |
Thomas Kruse1, Nadine Biedenkopf2, Emil Peter Thrane Hertz1, Erik Dietzel2, Gertrud Stalmann2, Blanca López-Méndez1, Norman E Davey3, Jakob Nilsson4, Stephan Becker5.
Abstract
Transcription of the Ebola virus genome depends on the viral transcription factor VP30 in its unphosphorylated form, but the underlying molecular mechanism of VP30 dephosphorylation is unknown. Here we show that the Ebola virus nucleoprotein (NP) recruits the host PP2A-B56 protein phosphatase through a B56-binding LxxIxE motif and that this motif is essential for VP30 dephosphorylation and viral transcription. The LxxIxE motif and the binding site of VP30 in NP are in close proximity, and both binding sites are required for the dephosphorylation of VP30. We generate a specific inhibitor of PP2A-B56 and show that it suppresses Ebola virus transcription and infection. This work dissects the molecular mechanism of VP30 dephosphorylation by PP2A-B56, and it pinpoints this phosphatase as a potential target for therapeutic intervention.Entities:
Keywords: B56; B’; Ebola virus; LxxIxE; NP; PP2A; VP30; filovirus; nucleoprotein; transcription regulation
Mesh:
Substances:
Year: 2017 PMID: 29290611 DOI: 10.1016/j.molcel.2017.11.034
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970