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The Diverse Roles of microRNAs at the Host–Virus Interface

MicroRNAs (miRNAs) are small, non-coding RNAs that regulate gene expression at the post-transcriptional level. Through this activity, they are implicated in almost every cellular process investigated to date. Hence, it is not surprising that miRNAs play diverse roles in regulation of viral infection...

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Detalles Bibliográficos
Autores principales: Bernier, Annie, Sagan, Selena M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116274/
https://www.ncbi.nlm.nih.gov/pubmed/30126238
http://dx.doi.org/10.3390/v10080440
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author Bernier, Annie
Sagan, Selena M.
author_facet Bernier, Annie
Sagan, Selena M.
author_sort Bernier, Annie
collection PubMed
description MicroRNAs (miRNAs) are small, non-coding RNAs that regulate gene expression at the post-transcriptional level. Through this activity, they are implicated in almost every cellular process investigated to date. Hence, it is not surprising that miRNAs play diverse roles in regulation of viral infections and antiviral responses. Diverse families of DNA and RNA viruses have been shown to take advantage of cellular miRNAs or produce virally encoded miRNAs that alter host or viral gene expression. MiRNA-mediated changes in gene expression have been demonstrated to modulate viral replication, antiviral immune responses, viral latency, and pathogenesis. Interestingly, viruses mediate both canonical and non-canonical interactions with miRNAs to downregulate specific targets or to promote viral genome stability, translation, and/or RNA accumulation. In this review, we focus on recent findings elucidating several key mechanisms employed by diverse virus families, with a focus on miRNAs at the host–virus interface during herpesvirus, polyomavirus, retroviruses, pestivirus, and hepacivirus infections.
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spelling pubmed-61162742018-08-31 The Diverse Roles of microRNAs at the Host–Virus Interface Bernier, Annie Sagan, Selena M. Viruses Review MicroRNAs (miRNAs) are small, non-coding RNAs that regulate gene expression at the post-transcriptional level. Through this activity, they are implicated in almost every cellular process investigated to date. Hence, it is not surprising that miRNAs play diverse roles in regulation of viral infections and antiviral responses. Diverse families of DNA and RNA viruses have been shown to take advantage of cellular miRNAs or produce virally encoded miRNAs that alter host or viral gene expression. MiRNA-mediated changes in gene expression have been demonstrated to modulate viral replication, antiviral immune responses, viral latency, and pathogenesis. Interestingly, viruses mediate both canonical and non-canonical interactions with miRNAs to downregulate specific targets or to promote viral genome stability, translation, and/or RNA accumulation. In this review, we focus on recent findings elucidating several key mechanisms employed by diverse virus families, with a focus on miRNAs at the host–virus interface during herpesvirus, polyomavirus, retroviruses, pestivirus, and hepacivirus infections. MDPI 2018-08-19 /pmc/articles/PMC6116274/ /pubmed/30126238 http://dx.doi.org/10.3390/v10080440 Text en © 2018 by the authors. 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
Bernier, Annie
Sagan, Selena M.
The Diverse Roles of microRNAs at the Host–Virus Interface
title The Diverse Roles of microRNAs at the Host–Virus Interface
title_full The Diverse Roles of microRNAs at the Host–Virus Interface
title_fullStr The Diverse Roles of microRNAs at the Host–Virus Interface
title_full_unstemmed The Diverse Roles of microRNAs at the Host–Virus Interface
title_short The Diverse Roles of microRNAs at the Host–Virus Interface
title_sort diverse roles of micrornas at the host–virus interface
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116274/
https://www.ncbi.nlm.nih.gov/pubmed/30126238
http://dx.doi.org/10.3390/v10080440
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