TY - JOUR
AU - Kamel, Wael
AU - Noerenberg, Marko
AU - Cerikan, Berat
AU - Chen, Honglin
AU - Järvelin, Aino I.
AU - Kammoun, Mohamed
AU - Lee, Jeffrey Y.
AU - Shuai, Ni
AU - Garcia-Moreno, Manuel
AU - Andrejeva, Anna
AU - Deery, Michael J.
AU - Johnson, Natasha
AU - Neufeldt, Christopher J.
AU - Cortese, Mirko
AU - Knight, Michael L.
AU - Lilley, Kathryn S.
AU - Martinez, Javier
AU - Davis, Ilan
AU - Bartenschlager, Ralf
AU - Mohammed, Shabaz
AU - Castello, Alfredo
PY - 2021
DA - May
TI - Global analysis of protein-RNA interactions in SARS-CoV-2 infected cells reveals key regulators of infection
JO - Molecular Cell
DO - http://dx.doi.org/10.1016/j.molcel.2021.05.023
AB - Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes COVID-19. SARS-CoV-2 relies on cellular RNA-binding proteins (RBPs) to replicate and spread, although which RBPs control its life cycle remains largely unknown. Here, we employ a multi-omic approach to identify systematically and comprehensively the cellular and viral RBPs that are involved in SARS-CoV-2 infection. We reveal that SARS-CoV-2 infection profoundly remodels the cellular RNA-bound proteome, which includes wide-ranging effects on RNA metabolic pathways, non-canonical RBPs and antiviral factors. Moreover, we apply a new method to identify the proteins that directly interact with viral RNA, uncovering dozens of cellular RBPs and six viral proteins. Amongst them, several components of the tRNA ligase complex, which we show regulate SARS-CoV-2 infection. Furthermore, we discover that available drugs targeting host RBPs that interact with SARS-CoV-2 RNA inhibit infection. Collectively, our results uncover a new universe of host-virus interactions with potential for new antiviral therapies against COVID-19.
PB - Elsevier
UR - http://eprints.gla.ac.uk/240311/
KW - Coronavirus (COVID-19)
ER