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Novel circRNA discovery in sheep shows evidence of high backsplice junction conservation
Circular RNAs (circRNAs) are covalently closed circular non-coding RNAs. Due to their structure, circRNAs are more stable and have longer half-lives than linear RNAs making them good candidates for disease biomarkers. Despite the scientific relevance of these molecules, the study of circRNAs in non-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801505/ https://www.ncbi.nlm.nih.gov/pubmed/33432020 http://dx.doi.org/10.1038/s41598-020-79781-2 |
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author | Varela-Martínez, Endika Corsi, Giulia I. Anthon, Christian Gorodkin, Jan Jugo, Begoña M. |
author_facet | Varela-Martínez, Endika Corsi, Giulia I. Anthon, Christian Gorodkin, Jan Jugo, Begoña M. |
author_sort | Varela-Martínez, Endika |
collection | PubMed |
description | Circular RNAs (circRNAs) are covalently closed circular non-coding RNAs. Due to their structure, circRNAs are more stable and have longer half-lives than linear RNAs making them good candidates for disease biomarkers. Despite the scientific relevance of these molecules, the study of circRNAs in non-model organisms is still in its infancy. Here, we analyse total RNA-seq data to identify circRNAs in sheep from peripheral blood mononuclear cells (PBMCs) and parietal lobe cortex. Out of 2510 and 3403 circRNAs detected in parietal lobe cortex and in PBMCs, a total of 1379 novel circRNAs were discovered. Remarkably, around 63% of all detected circRNAs were found to be completely homologous to a circRNA annotated in human. Functional enrichment analysis was conducted for both tissues based on GO terms and KEGG pathways. The enriched terms suggest an important role of circRNAs from encephalon in synaptic functions and the involvement of circRNAs from PBMCs in basic immune system functions. In addition to this, we investigated the role of circRNAs in repetitive vaccination experiments via differential expression analysis and did not detect any significant relationship. At last, our results support both the miRNA sponge and the miRNA shuttle functions of CDR1-AS in sheep brain. To our knowledge, this is the first study on circRNA annotation in sheep PBMCs or parietal lobe cortex samples. |
format | Online Article Text |
id | pubmed-7801505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78015052021-01-12 Novel circRNA discovery in sheep shows evidence of high backsplice junction conservation Varela-Martínez, Endika Corsi, Giulia I. Anthon, Christian Gorodkin, Jan Jugo, Begoña M. Sci Rep Article Circular RNAs (circRNAs) are covalently closed circular non-coding RNAs. Due to their structure, circRNAs are more stable and have longer half-lives than linear RNAs making them good candidates for disease biomarkers. Despite the scientific relevance of these molecules, the study of circRNAs in non-model organisms is still in its infancy. Here, we analyse total RNA-seq data to identify circRNAs in sheep from peripheral blood mononuclear cells (PBMCs) and parietal lobe cortex. Out of 2510 and 3403 circRNAs detected in parietal lobe cortex and in PBMCs, a total of 1379 novel circRNAs were discovered. Remarkably, around 63% of all detected circRNAs were found to be completely homologous to a circRNA annotated in human. Functional enrichment analysis was conducted for both tissues based on GO terms and KEGG pathways. The enriched terms suggest an important role of circRNAs from encephalon in synaptic functions and the involvement of circRNAs from PBMCs in basic immune system functions. In addition to this, we investigated the role of circRNAs in repetitive vaccination experiments via differential expression analysis and did not detect any significant relationship. At last, our results support both the miRNA sponge and the miRNA shuttle functions of CDR1-AS in sheep brain. To our knowledge, this is the first study on circRNA annotation in sheep PBMCs or parietal lobe cortex samples. Nature Publishing Group UK 2021-01-11 /pmc/articles/PMC7801505/ /pubmed/33432020 http://dx.doi.org/10.1038/s41598-020-79781-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Varela-Martínez, Endika Corsi, Giulia I. Anthon, Christian Gorodkin, Jan Jugo, Begoña M. Novel circRNA discovery in sheep shows evidence of high backsplice junction conservation |
title | Novel circRNA discovery in sheep shows evidence of high backsplice junction conservation |
title_full | Novel circRNA discovery in sheep shows evidence of high backsplice junction conservation |
title_fullStr | Novel circRNA discovery in sheep shows evidence of high backsplice junction conservation |
title_full_unstemmed | Novel circRNA discovery in sheep shows evidence of high backsplice junction conservation |
title_short | Novel circRNA discovery in sheep shows evidence of high backsplice junction conservation |
title_sort | novel circrna discovery in sheep shows evidence of high backsplice junction conservation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801505/ https://www.ncbi.nlm.nih.gov/pubmed/33432020 http://dx.doi.org/10.1038/s41598-020-79781-2 |
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