RACK1 Associates with RNA-Binding Proteins Vigilin and SERBP1 to Facilitate Dengue Virus Replication

Alexis Brugier(Centre National de la Recherche Scientifique), Mohamed Lamine Hafirrassou(Centre National de la Recherche Scientifique), Marie Pourcelot(Centre National de la Recherche Scientifique), Morgane Baldaccini(Centre National de la Recherche Scientifique), Vasiliya Kril(Centre National de la Recherche Scientifique), Laurine Couture(Centre National de la Recherche Scientifique), Beate M. Kümmerer(University of Bonn), Sarah Gallois‐Montbrun(Centre National de la Recherche Scientifique), Lucie Bonnet‐Madin(Centre National de la Recherche Scientifique), Pierre‐Olivier Vidalain(Université Claude Bernard Lyon 1), Constance Delaugerre(Centre National de la Recherche Scientifique), Sébastien Pfeffer(Centre National de la Recherche Scientifique), Laurent Meertens(Centre National de la Recherche Scientifique), Ali Amara(Centre National de la Recherche Scientifique)
Journal of Virology
March 10, 2022
Cited by 43Open Access
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Abstract

We recently identified the scaffolding RACK1 protein as an important host-dependency factor for dengue virus (DENV), a positive-stranded RNA virus responsible for the most prevalent mosquito-borne viral disease worldwide. Here, we have performed the first RACK1 interactome in human cells and identified Vigilin and SERBP1 as DENV host-dependency factors. Both are RNA-binding proteins that interact with the DENV RNA to regulate viral replication. Importantly, Vigilin and SERBP1 interact with RACK1 and the DENV viral RNA (vRNA) to mediate viral replication. Overall, our results suggest that RACK1 acts as a binding platform at the surface of the 40S ribosomal subunit to recruit Vigilin and SERBP1, which may therefore function as linkers between the viral RNA and the translation machinery to facilitate infection.


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