The importance of virion-incorporated cellular RNA-Binding Proteins in viral particle assembly and infectivity. (March 2021)

• Record Type: Journal Article
• Authors: Dicker, Kate; Järvelin, Aino I.; Garcia-Moreno, Manuel; Castello, Alfredo
• Is Part Of: Seminars in cell & developmental biology. Volume 111(2021)
• Page Start: 108
• Page End: 118
• Publication Date: 2021-03
• Subjects: 4SU 4-thiouridine -- CLIP-seq Crosslinking and immunoprecipitation followed by sequencing -- DENV Dengue virus -- dsDNA Double-stranded DNA -- dsRNA Double-stranded RNA -- GO Gene Ontology -- HBV Hepatitis B virus -- HCV Hepatitis C virus -- HIV-1 Human immunodeficiency virus 1 -- IAV Influenza A virus -- ivRBP In virion RNA-binding protein -- MeV Measles virus -- PAMP Pathogen associated molecular pattern -- pgRNA Pre-genomic RNA -- RBD RNA-binding domain -- RBP RNA-binding protein -- RIC RNA-interactome capture -- RNP Ribonucleoprotein -- RRM RNA-recognition motif -- RSV Respiratory syncytial virus -- RVFV Rift Valley fever virus -- SINV Sindbis virus -- vRNA Viral RNA -- vRNP Viral ribonucleoprotein -- VSV Vesicular stomatitis virus -- ZIKV Zika virus; RNA-binding protein -- Virus -- Protein-RNA interaction -- Virus infection -- Virus assembly -- Virus replication -- RBP; Cytology -- Periodicals; Developmental biology -- Periodicals; 571.6
• DOI: 10.1016/j.semcdb.2020.08.002
• Languages: English
• ISSNs: 1084-9521

Abstract

Highlights: Proteomic studies have uncovered more than a thousand cellular proteins that are present in the particles of RNA viruses. Strikingly, nearly four hundred of these are RNA-binding proteins (RBPs). Several virion-incorporated RBPs have been shown to regulate viral particle assembly and the initial steps of infection. These host RBPs with regulatory roles in infection represent potential targets for antiviral therapy. Abstract: RNA is a central molecule in RNA virus biology due to its dual function as messenger and genome. However, the small number of proteins encoded by viral genomes is insufficient to enable virus infection. Hence, viruses hijack cellular RNA-binding proteins (RBPs) to aid replication and spread. In this review we discuss the 'knowns' and 'unknowns' regarding the contribution of host RBPs to the formation of viral particles and the initial steps of infection in the newly infected cell. Through comparison of the virion proteomes of ten different human RNA viruses, we confirm that a pool of cellular RBPs are typically incorporated into viral particles. We describe here illustrative examples supporting the important functions of these RBPs in viral particle formation and infectivity and we propose that the role of host RBPs in these steps can be broader than previously anticipated. Understanding how cellular RBPs regulate virus infection can lead to the discovery of novel therapeutic targets against viruses.