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Circular RNAs: A novel type of non-coding RNA and their potential implications in antiviral immunity
Circular RNAs (circRNAs), a novel type of non-coding RNAs (ncRNAs), are ubiquitously expressed in eukaryotic cells during post-transcriptional processes. Unlike linear RNAs, circRNAs form covalent-closed continuous loops without 5' to 3' polarities and poly (A) tails. With advances in high...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Ivyspring International Publisher
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723916/ https://www.ncbi.nlm.nih.gov/pubmed/29230098 http://dx.doi.org/10.7150/ijbs.22531 |
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author | Wang, Man Yu, Fei Wu, Wei Zhang, Yuan Chang, Wenguang Ponnusamy, Murugavel Wang, Kun Li, Peifeng |
author_facet | Wang, Man Yu, Fei Wu, Wei Zhang, Yuan Chang, Wenguang Ponnusamy, Murugavel Wang, Kun Li, Peifeng |
author_sort | Wang, Man |
collection | PubMed |
description | Circular RNAs (circRNAs), a novel type of non-coding RNAs (ncRNAs), are ubiquitously expressed in eukaryotic cells during post-transcriptional processes. Unlike linear RNAs, circRNAs form covalent-closed continuous loops without 5' to 3' polarities and poly (A) tails. With advances in high-throughput sequencing technology, numerous circRNAs have been identified in plants, animals and humans. Notably, circRNAs display cell-type, tissue-type and developmental-stage specific expression patterns in eukaryotic transcriptome, which reveals their significant regulatory functions in gene expression. More importantly, circRNAs serve as microRNA (miRNA) sponges and crucial regulators of gene expression. Additionally, circRNAs modulate pre-mRNA alternative splicing and possess protein-coding capacity. CircRNAs exhibit altered expression under pathological conditions and are strongly associated with the development of various human diseases. Interestingly, circRNAs can also induce antiviral immune responses. A recent study found that the delivery of circRNAs generated in vitro activates RIG-I-mediated innate immune responses and provides protection against viral infection. The antiviral dsRNA-binding proteins, NF90/NF110, act as key regulators in circRNA biogenesis. NF90/NF110 are also functional in inhibiting viral replication through binding to viral mRNAs. In this review, we provide a comprehensive overview on the classification, biogenesis and functions of circRNAs. We also discuss the critical role of circRNAs in eliciting antiviral immunity, providing evidence for the potential implications of circRNAs in antiviral therapies. |
format | Online Article Text |
id | pubmed-5723916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-57239162017-12-11 Circular RNAs: A novel type of non-coding RNA and their potential implications in antiviral immunity Wang, Man Yu, Fei Wu, Wei Zhang, Yuan Chang, Wenguang Ponnusamy, Murugavel Wang, Kun Li, Peifeng Int J Biol Sci Review Circular RNAs (circRNAs), a novel type of non-coding RNAs (ncRNAs), are ubiquitously expressed in eukaryotic cells during post-transcriptional processes. Unlike linear RNAs, circRNAs form covalent-closed continuous loops without 5' to 3' polarities and poly (A) tails. With advances in high-throughput sequencing technology, numerous circRNAs have been identified in plants, animals and humans. Notably, circRNAs display cell-type, tissue-type and developmental-stage specific expression patterns in eukaryotic transcriptome, which reveals their significant regulatory functions in gene expression. More importantly, circRNAs serve as microRNA (miRNA) sponges and crucial regulators of gene expression. Additionally, circRNAs modulate pre-mRNA alternative splicing and possess protein-coding capacity. CircRNAs exhibit altered expression under pathological conditions and are strongly associated with the development of various human diseases. Interestingly, circRNAs can also induce antiviral immune responses. A recent study found that the delivery of circRNAs generated in vitro activates RIG-I-mediated innate immune responses and provides protection against viral infection. The antiviral dsRNA-binding proteins, NF90/NF110, act as key regulators in circRNA biogenesis. NF90/NF110 are also functional in inhibiting viral replication through binding to viral mRNAs. In this review, we provide a comprehensive overview on the classification, biogenesis and functions of circRNAs. We also discuss the critical role of circRNAs in eliciting antiviral immunity, providing evidence for the potential implications of circRNAs in antiviral therapies. Ivyspring International Publisher 2017-11-02 /pmc/articles/PMC5723916/ /pubmed/29230098 http://dx.doi.org/10.7150/ijbs.22531 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Wang, Man Yu, Fei Wu, Wei Zhang, Yuan Chang, Wenguang Ponnusamy, Murugavel Wang, Kun Li, Peifeng Circular RNAs: A novel type of non-coding RNA and their potential implications in antiviral immunity |
title | Circular RNAs: A novel type of non-coding RNA and their potential implications in antiviral immunity |
title_full | Circular RNAs: A novel type of non-coding RNA and their potential implications in antiviral immunity |
title_fullStr | Circular RNAs: A novel type of non-coding RNA and their potential implications in antiviral immunity |
title_full_unstemmed | Circular RNAs: A novel type of non-coding RNA and their potential implications in antiviral immunity |
title_short | Circular RNAs: A novel type of non-coding RNA and their potential implications in antiviral immunity |
title_sort | circular rnas: a novel type of non-coding rna and their potential implications in antiviral immunity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723916/ https://www.ncbi.nlm.nih.gov/pubmed/29230098 http://dx.doi.org/10.7150/ijbs.22531 |
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