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Regulation of Latency and Reactivation by Human Cytomegalovirus miRNAs

Human cytomegalovirus (HCMV) encodes 22 mature microRNAs (miRNAs), which regulate a myriad of cellular processes, including vesicular trafficking, cell cycle progression, apoptosis, and immune evasion, as well as viral gene expression. Recent evidence points to a critical role for HCMV miRNAs in med...

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Detalles Bibliográficos
Autores principales: Diggins, Nicole L., Skalsky, Rebecca L., Hancock, Meaghan H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918750/
https://www.ncbi.nlm.nih.gov/pubmed/33668486
http://dx.doi.org/10.3390/pathogens10020200
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author Diggins, Nicole L.
Skalsky, Rebecca L.
Hancock, Meaghan H.
author_facet Diggins, Nicole L.
Skalsky, Rebecca L.
Hancock, Meaghan H.
author_sort Diggins, Nicole L.
collection PubMed
description Human cytomegalovirus (HCMV) encodes 22 mature microRNAs (miRNAs), which regulate a myriad of cellular processes, including vesicular trafficking, cell cycle progression, apoptosis, and immune evasion, as well as viral gene expression. Recent evidence points to a critical role for HCMV miRNAs in mediating latency in CD34(+) hematopoietic progenitor cells through modulation of cellular signaling pathways, including attenuation of TGFβ and EGFR signaling. Moreover, HCMV miRNAs can act in concert with, or in opposition to, viral proteins in regulating host cell functions. Here, we comprehensively review the studies of HCMV miRNAs in the context of latency and highlight the novel processes that are manipulated by the virus using these small non-coding RNAs.
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spelling pubmed-79187502021-03-02 Regulation of Latency and Reactivation by Human Cytomegalovirus miRNAs Diggins, Nicole L. Skalsky, Rebecca L. Hancock, Meaghan H. Pathogens Review Human cytomegalovirus (HCMV) encodes 22 mature microRNAs (miRNAs), which regulate a myriad of cellular processes, including vesicular trafficking, cell cycle progression, apoptosis, and immune evasion, as well as viral gene expression. Recent evidence points to a critical role for HCMV miRNAs in mediating latency in CD34(+) hematopoietic progenitor cells through modulation of cellular signaling pathways, including attenuation of TGFβ and EGFR signaling. Moreover, HCMV miRNAs can act in concert with, or in opposition to, viral proteins in regulating host cell functions. Here, we comprehensively review the studies of HCMV miRNAs in the context of latency and highlight the novel processes that are manipulated by the virus using these small non-coding RNAs. MDPI 2021-02-13 /pmc/articles/PMC7918750/ /pubmed/33668486 http://dx.doi.org/10.3390/pathogens10020200 Text en © 2021 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
Diggins, Nicole L.
Skalsky, Rebecca L.
Hancock, Meaghan H.
Regulation of Latency and Reactivation by Human Cytomegalovirus miRNAs
title Regulation of Latency and Reactivation by Human Cytomegalovirus miRNAs
title_full Regulation of Latency and Reactivation by Human Cytomegalovirus miRNAs
title_fullStr Regulation of Latency and Reactivation by Human Cytomegalovirus miRNAs
title_full_unstemmed Regulation of Latency and Reactivation by Human Cytomegalovirus miRNAs
title_short Regulation of Latency and Reactivation by Human Cytomegalovirus miRNAs
title_sort regulation of latency and reactivation by human cytomegalovirus mirnas
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918750/
https://www.ncbi.nlm.nih.gov/pubmed/33668486
http://dx.doi.org/10.3390/pathogens10020200
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