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The importance of virion-incorporated cellular RNA-Binding Proteins in viral particle assembly and infectivity

期刊

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
卷 111, 期 -, 页码 108-118

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2020.08.002

关键词

RNA-binding protein; Virus; Protein-RNA interaction; Virus infection; Virus assembly; Virus replication; RBP

资金

  1. MRC Career Development Award [MR/L019434/1]
  2. MRC [MR/R021562/1]
  3. John Fell Funds from the University of Oxford [0006735]
  4. Wellcome Trust [BST00120]
  5. Wellcome [209412/Z/17/Z]
  6. Wellcome Trust [209412/Z/17/Z] Funding Source: Wellcome Trust
  7. MRC [MR/R021562/1] Funding Source: UKRI

向作者/读者索取更多资源

RNA viruses rely on cellular RNA-binding proteins to facilitate replication and spread, with a pool of RBPs typically incorporated into viral particles. These RBPs play crucial roles in viral particle formation and infectivity, suggesting broader implications for host RBPs in virus infection than previously thought.
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 `known' 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.

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