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Regulation of Ribosomal Proteins on Viral Infection

Ribosomal proteins (RPs), in conjunction with rRNA, are major components of ribosomes involved in the cellular process of protein biosynthesis, known as “translation”. The viruses, as the small infectious pathogens with limited genomes, must recruit a variety of host factors to survive and propagate...

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Autor principal: Li, Shuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562653/
https://www.ncbi.nlm.nih.gov/pubmed/31137833
http://dx.doi.org/10.3390/cells8050508
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author Li, Shuo
author_facet Li, Shuo
author_sort Li, Shuo
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description Ribosomal proteins (RPs), in conjunction with rRNA, are major components of ribosomes involved in the cellular process of protein biosynthesis, known as “translation”. The viruses, as the small infectious pathogens with limited genomes, must recruit a variety of host factors to survive and propagate, including RPs. At present, more and more information is available on the functional relationship between RPs and virus infection. This review focuses on advancements in my own understanding of critical roles of RPs in the life cycle of viruses. Various RPs interact with viral mRNA and proteins to participate in viral protein biosynthesis and regulate the replication and infection of virus in host cells. Most interactions are essential for viral translation and replication, which promote viral infection and accumulation, whereas the minority represents the defense signaling of host cells by activating immune pathway against virus. RPs provide a new platform for antiviral therapy development, however, at present, antiviral therapeutics with RPs involving in virus infection as targets is limited, and exploring antiviral strategy based on RPs will be the guides for further study.
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spelling pubmed-65626532019-06-17 Regulation of Ribosomal Proteins on Viral Infection Li, Shuo Cells Review Ribosomal proteins (RPs), in conjunction with rRNA, are major components of ribosomes involved in the cellular process of protein biosynthesis, known as “translation”. The viruses, as the small infectious pathogens with limited genomes, must recruit a variety of host factors to survive and propagate, including RPs. At present, more and more information is available on the functional relationship between RPs and virus infection. This review focuses on advancements in my own understanding of critical roles of RPs in the life cycle of viruses. Various RPs interact with viral mRNA and proteins to participate in viral protein biosynthesis and regulate the replication and infection of virus in host cells. Most interactions are essential for viral translation and replication, which promote viral infection and accumulation, whereas the minority represents the defense signaling of host cells by activating immune pathway against virus. RPs provide a new platform for antiviral therapy development, however, at present, antiviral therapeutics with RPs involving in virus infection as targets is limited, and exploring antiviral strategy based on RPs will be the guides for further study. MDPI 2019-05-27 /pmc/articles/PMC6562653/ /pubmed/31137833 http://dx.doi.org/10.3390/cells8050508 Text en © 2019 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Li, Shuo
Regulation of Ribosomal Proteins on Viral Infection
title Regulation of Ribosomal Proteins on Viral Infection
title_full Regulation of Ribosomal Proteins on Viral Infection
title_fullStr Regulation of Ribosomal Proteins on Viral Infection
title_full_unstemmed Regulation of Ribosomal Proteins on Viral Infection
title_short Regulation of Ribosomal Proteins on Viral Infection
title_sort regulation of ribosomal proteins on viral infection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562653/
https://www.ncbi.nlm.nih.gov/pubmed/31137833
http://dx.doi.org/10.3390/cells8050508
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