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The Role of the Z-DNA Binding Domain in Innate Immunity and Stress Granules

Both DNA and RNA can maintain left-handed double helical Z-conformation under physiological condition, but only when stabilized by Z-DNA binding domain (ZDBD). After initial discovery in RNA editing enzyme ADAR1, ZDBD has also been described in pathogen-sensing proteins ZBP1 and PKZ in host, as well...

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Autores principales: Chiang, De Chen, Li, Yan, Ng, Siew Kit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886975/
https://www.ncbi.nlm.nih.gov/pubmed/33613567
http://dx.doi.org/10.3389/fimmu.2020.625504
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author Chiang, De Chen
Li, Yan
Ng, Siew Kit
author_facet Chiang, De Chen
Li, Yan
Ng, Siew Kit
author_sort Chiang, De Chen
collection PubMed
description Both DNA and RNA can maintain left-handed double helical Z-conformation under physiological condition, but only when stabilized by Z-DNA binding domain (ZDBD). After initial discovery in RNA editing enzyme ADAR1, ZDBD has also been described in pathogen-sensing proteins ZBP1 and PKZ in host, as well as virulence proteins E3L and ORF112 in viruses. The host-virus antagonism immediately highlights the importance of ZDBD in antiviral innate immunity. Furthermore, Z-RNA binding has been shown to be responsible for the localization of these ZDBD-containing proteins to cytoplasmic stress granules that play central role in coordinating cellular response to stresses. This review sought to consolidate current understanding of Z-RNA sensing in innate immunity and implore possible roles of Z-RNA binding within cytoplasmic stress granules.
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spelling pubmed-78869752021-02-18 The Role of the Z-DNA Binding Domain in Innate Immunity and Stress Granules Chiang, De Chen Li, Yan Ng, Siew Kit Front Immunol Immunology Both DNA and RNA can maintain left-handed double helical Z-conformation under physiological condition, but only when stabilized by Z-DNA binding domain (ZDBD). After initial discovery in RNA editing enzyme ADAR1, ZDBD has also been described in pathogen-sensing proteins ZBP1 and PKZ in host, as well as virulence proteins E3L and ORF112 in viruses. The host-virus antagonism immediately highlights the importance of ZDBD in antiviral innate immunity. Furthermore, Z-RNA binding has been shown to be responsible for the localization of these ZDBD-containing proteins to cytoplasmic stress granules that play central role in coordinating cellular response to stresses. This review sought to consolidate current understanding of Z-RNA sensing in innate immunity and implore possible roles of Z-RNA binding within cytoplasmic stress granules. Frontiers Media S.A. 2021-02-03 /pmc/articles/PMC7886975/ /pubmed/33613567 http://dx.doi.org/10.3389/fimmu.2020.625504 Text en Copyright © 2021 Chiang, Li and Ng http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Chiang, De Chen
Li, Yan
Ng, Siew Kit
The Role of the Z-DNA Binding Domain in Innate Immunity and Stress Granules
title The Role of the Z-DNA Binding Domain in Innate Immunity and Stress Granules
title_full The Role of the Z-DNA Binding Domain in Innate Immunity and Stress Granules
title_fullStr The Role of the Z-DNA Binding Domain in Innate Immunity and Stress Granules
title_full_unstemmed The Role of the Z-DNA Binding Domain in Innate Immunity and Stress Granules
title_short The Role of the Z-DNA Binding Domain in Innate Immunity and Stress Granules
title_sort role of the z-dna binding domain in innate immunity and stress granules
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886975/
https://www.ncbi.nlm.nih.gov/pubmed/33613567
http://dx.doi.org/10.3389/fimmu.2020.625504
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