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RNase T2 in Inflammation and Cancer: Immunological and Biological Views

The RNase T2 family consists of evolutionarily conserved endonucleases that express in many different species, including animals, plants, protozoans, bacteria, and viruses. The main biological roles of these ribonucleases are cleaving or degrading RNA substrates. They preferentially cleave single-st...

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Detalles Bibliográficos
Autores principales: Wu, Lei, Xu, Yanquan, Zhao, Huakan, Li, Yongsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438567/
https://www.ncbi.nlm.nih.gov/pubmed/32903619
http://dx.doi.org/10.3389/fimmu.2020.01554
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author Wu, Lei
Xu, Yanquan
Zhao, Huakan
Li, Yongsheng
author_facet Wu, Lei
Xu, Yanquan
Zhao, Huakan
Li, Yongsheng
author_sort Wu, Lei
collection PubMed
description The RNase T2 family consists of evolutionarily conserved endonucleases that express in many different species, including animals, plants, protozoans, bacteria, and viruses. The main biological roles of these ribonucleases are cleaving or degrading RNA substrates. They preferentially cleave single-stranded RNA molecules between purine and uridine residues to generate two nucleotide fragments with 2'3'-cyclic phosphate adenosine/guanosine terminus and uridine residue, respectively. Accumulating studies have revealed that RNase T2 is critical for the pathophysiology of inflammation and cancer. In this review, we introduce the distribution, structure, and functions of RNase T2, its differential roles in inflammation and cancer, and the perspective for its research and related applications in medicine.
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spelling pubmed-74385672020-09-03 RNase T2 in Inflammation and Cancer: Immunological and Biological Views Wu, Lei Xu, Yanquan Zhao, Huakan Li, Yongsheng Front Immunol Immunology The RNase T2 family consists of evolutionarily conserved endonucleases that express in many different species, including animals, plants, protozoans, bacteria, and viruses. The main biological roles of these ribonucleases are cleaving or degrading RNA substrates. They preferentially cleave single-stranded RNA molecules between purine and uridine residues to generate two nucleotide fragments with 2'3'-cyclic phosphate adenosine/guanosine terminus and uridine residue, respectively. Accumulating studies have revealed that RNase T2 is critical for the pathophysiology of inflammation and cancer. In this review, we introduce the distribution, structure, and functions of RNase T2, its differential roles in inflammation and cancer, and the perspective for its research and related applications in medicine. Frontiers Media S.A. 2020-08-13 /pmc/articles/PMC7438567/ /pubmed/32903619 http://dx.doi.org/10.3389/fimmu.2020.01554 Text en Copyright © 2020 Wu, Xu, Zhao and Li. 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
Wu, Lei
Xu, Yanquan
Zhao, Huakan
Li, Yongsheng
RNase T2 in Inflammation and Cancer: Immunological and Biological Views
title RNase T2 in Inflammation and Cancer: Immunological and Biological Views
title_full RNase T2 in Inflammation and Cancer: Immunological and Biological Views
title_fullStr RNase T2 in Inflammation and Cancer: Immunological and Biological Views
title_full_unstemmed RNase T2 in Inflammation and Cancer: Immunological and Biological Views
title_short RNase T2 in Inflammation and Cancer: Immunological and Biological Views
title_sort rnase t2 in inflammation and cancer: immunological and biological views
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438567/
https://www.ncbi.nlm.nih.gov/pubmed/32903619
http://dx.doi.org/10.3389/fimmu.2020.01554
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