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lncRNA-mediated regulation of the interferon response

The interferon (IFN) response is a critical arm of the innate immune response and a major host defense mechanism against viral infections. Following microbial encounter, a series of signaling events lead to transcriptional activation of the IFN genes, which in turn leads to significant changes in th...

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Detalles Bibliográficos
Autores principales: Valadkhan, Saba, Gunawardane, Lalith S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744491/
https://www.ncbi.nlm.nih.gov/pubmed/26474526
http://dx.doi.org/10.1016/j.virusres.2015.09.023
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author Valadkhan, Saba
Gunawardane, Lalith S.
author_facet Valadkhan, Saba
Gunawardane, Lalith S.
author_sort Valadkhan, Saba
collection PubMed
description The interferon (IFN) response is a critical arm of the innate immune response and a major host defense mechanism against viral infections. Following microbial encounter, a series of signaling events lead to transcriptional activation of the IFN genes, which in turn leads to significant changes in the cellular transcriptome by altering the expression of hundreds of target genes. Emerging evidence suggests that long non-coding RNAs (lncRNAs) constitute a major subgroup of the IFN target genes, and further, that the IFN response is subject to regulation by a large number of host- and pathogen-derived lncRNAs. While the vast majority of lncRNAs with potential roles in the IFN response remain unstudied, analysis of a very small subset provides a glimpse of the regulatory impact of this class of RNAs on IFN response.
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spelling pubmed-47444912017-01-02 lncRNA-mediated regulation of the interferon response Valadkhan, Saba Gunawardane, Lalith S. Virus Res Article The interferon (IFN) response is a critical arm of the innate immune response and a major host defense mechanism against viral infections. Following microbial encounter, a series of signaling events lead to transcriptional activation of the IFN genes, which in turn leads to significant changes in the cellular transcriptome by altering the expression of hundreds of target genes. Emerging evidence suggests that long non-coding RNAs (lncRNAs) constitute a major subgroup of the IFN target genes, and further, that the IFN response is subject to regulation by a large number of host- and pathogen-derived lncRNAs. While the vast majority of lncRNAs with potential roles in the IFN response remain unstudied, analysis of a very small subset provides a glimpse of the regulatory impact of this class of RNAs on IFN response. Elsevier B.V. 2016-01-02 2015-10-22 /pmc/articles/PMC4744491/ /pubmed/26474526 http://dx.doi.org/10.1016/j.virusres.2015.09.023 Text en Copyright © 2015 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Valadkhan, Saba
Gunawardane, Lalith S.
lncRNA-mediated regulation of the interferon response
title lncRNA-mediated regulation of the interferon response
title_full lncRNA-mediated regulation of the interferon response
title_fullStr lncRNA-mediated regulation of the interferon response
title_full_unstemmed lncRNA-mediated regulation of the interferon response
title_short lncRNA-mediated regulation of the interferon response
title_sort lncrna-mediated regulation of the interferon response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744491/
https://www.ncbi.nlm.nih.gov/pubmed/26474526
http://dx.doi.org/10.1016/j.virusres.2015.09.023
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