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CircRNA accumulation in the aging mouse brain
Circular RNAs (circRNAs) are a newly appreciated class of RNAs expressed across diverse phyla. These enigmatic transcripts are most commonly generated by back-splicing events from exons of protein-coding genes. This results in highly stable RNAs due to the lack of free 5′ and 3′ ends. CircRNAs are e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153657/ https://www.ncbi.nlm.nih.gov/pubmed/27958329 http://dx.doi.org/10.1038/srep38907 |
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author | Gruner, Hannah Cortés-López, Mariela Cooper, Daphne A. Bauer, Matthew Miura, Pedro |
author_facet | Gruner, Hannah Cortés-López, Mariela Cooper, Daphne A. Bauer, Matthew Miura, Pedro |
author_sort | Gruner, Hannah |
collection | PubMed |
description | Circular RNAs (circRNAs) are a newly appreciated class of RNAs expressed across diverse phyla. These enigmatic transcripts are most commonly generated by back-splicing events from exons of protein-coding genes. This results in highly stable RNAs due to the lack of free 5′ and 3′ ends. CircRNAs are enriched in neural tissues, suggesting that they might have neural functions. Here, we sought to determine whether circRNA accumulation occurs during aging in mice. Total RNA-seq profiling of young (1 month old) and aged (22 month old) cortex, hippocampus and heart samples was performed. This led to the confident detection of 6,791 distinct circRNAs across these samples, including 675 novel circRNAs. Analysis uncovered a strong bias for circRNA upregulation during aging in neural tissues. These age-accumulation trends were verified for individual circRNAs by RT-qPCR and Northern analysis. In contrast, comparison of aged versus young hearts failed to reveal a global trend for circRNA upregulation. Age-accumulation of circRNAs in brain tissues was found to be largely independent from linear RNA expression of host genes. These findings suggest that circRNAs might play biological roles relevant to the aging nervous system. |
format | Online Article Text |
id | pubmed-5153657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51536572016-12-28 CircRNA accumulation in the aging mouse brain Gruner, Hannah Cortés-López, Mariela Cooper, Daphne A. Bauer, Matthew Miura, Pedro Sci Rep Article Circular RNAs (circRNAs) are a newly appreciated class of RNAs expressed across diverse phyla. These enigmatic transcripts are most commonly generated by back-splicing events from exons of protein-coding genes. This results in highly stable RNAs due to the lack of free 5′ and 3′ ends. CircRNAs are enriched in neural tissues, suggesting that they might have neural functions. Here, we sought to determine whether circRNA accumulation occurs during aging in mice. Total RNA-seq profiling of young (1 month old) and aged (22 month old) cortex, hippocampus and heart samples was performed. This led to the confident detection of 6,791 distinct circRNAs across these samples, including 675 novel circRNAs. Analysis uncovered a strong bias for circRNA upregulation during aging in neural tissues. These age-accumulation trends were verified for individual circRNAs by RT-qPCR and Northern analysis. In contrast, comparison of aged versus young hearts failed to reveal a global trend for circRNA upregulation. Age-accumulation of circRNAs in brain tissues was found to be largely independent from linear RNA expression of host genes. These findings suggest that circRNAs might play biological roles relevant to the aging nervous system. Nature Publishing Group 2016-12-13 /pmc/articles/PMC5153657/ /pubmed/27958329 http://dx.doi.org/10.1038/srep38907 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gruner, Hannah Cortés-López, Mariela Cooper, Daphne A. Bauer, Matthew Miura, Pedro CircRNA accumulation in the aging mouse brain |
title | CircRNA accumulation in the aging mouse brain |
title_full | CircRNA accumulation in the aging mouse brain |
title_fullStr | CircRNA accumulation in the aging mouse brain |
title_full_unstemmed | CircRNA accumulation in the aging mouse brain |
title_short | CircRNA accumulation in the aging mouse brain |
title_sort | circrna accumulation in the aging mouse brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153657/ https://www.ncbi.nlm.nih.gov/pubmed/27958329 http://dx.doi.org/10.1038/srep38907 |
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