Cargando…
Global accumulation of circRNAs during aging in Caenorhabditis elegans
BACKGROUND: Circular RNAs (CircRNAs) are a newly appreciated class of RNAs that lack free 5′ and 3′ ends, are expressed by the thousands in diverse forms of life, and are mostly of enigmatic function. Ostensibly due to their resistance to exonucleases, circRNAs are known to be exceptionally stable....
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753478/ https://www.ncbi.nlm.nih.gov/pubmed/29298683 http://dx.doi.org/10.1186/s12864-017-4386-y |
_version_ | 1783290278613876736 |
---|---|
author | Cortés-López, Mariela Gruner, Matthew R. Cooper, Daphne A. Gruner, Hannah N. Voda, Alexandru-Ioan van der Linden, Alexander M. Miura, Pedro |
author_facet | Cortés-López, Mariela Gruner, Matthew R. Cooper, Daphne A. Gruner, Hannah N. Voda, Alexandru-Ioan van der Linden, Alexander M. Miura, Pedro |
author_sort | Cortés-López, Mariela |
collection | PubMed |
description | BACKGROUND: Circular RNAs (CircRNAs) are a newly appreciated class of RNAs that lack free 5′ and 3′ ends, are expressed by the thousands in diverse forms of life, and are mostly of enigmatic function. Ostensibly due to their resistance to exonucleases, circRNAs are known to be exceptionally stable. Previous work in Drosophila and mice have shown that circRNAs increase during aging in neural tissues. RESULTS: Here, we examined the global profile of circRNAs in C. elegans during aging by performing ribo-depleted total RNA-seq from the fourth larval stage (L4) through 10-day old adults. Using stringent bioinformatic criteria and experimental validation, we annotated a high-confidence set of 1166 circRNAs, including 575 newly discovered circRNAs. These circRNAs were derived from 797 genes with diverse functions, including genes involved in the determination of lifespan. A massive accumulation of circRNAs during aging was uncovered. Many hundreds of circRNAs were significantly increased among the aging time-points and increases of select circRNAs by over 40-fold during aging were quantified by RT-qPCR. The expression of 459 circRNAs was determined to be distinct from the expression of linear RNAs from the same host genes, demonstrating host gene independence of circRNA age-accumulation. CONCLUSIONS: We attribute the global scale of circRNA age-accumulation to the high composition of post-mitotic cells in adult C. elegans, coupled with the high resistance of circRNAs to decay. These findings suggest that the exceptional stability of circRNAs might explain age-accumulation trends observed from neural tissues of other organisms, which also have a high composition of post-mitotic cells. Given the suitability of C. elegans for aging research, it is now poised as an excellent model system to determine whether there are functional consequences of circRNA accumulation during aging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4386-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5753478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57534782018-01-05 Global accumulation of circRNAs during aging in Caenorhabditis elegans Cortés-López, Mariela Gruner, Matthew R. Cooper, Daphne A. Gruner, Hannah N. Voda, Alexandru-Ioan van der Linden, Alexander M. Miura, Pedro BMC Genomics Research Article BACKGROUND: Circular RNAs (CircRNAs) are a newly appreciated class of RNAs that lack free 5′ and 3′ ends, are expressed by the thousands in diverse forms of life, and are mostly of enigmatic function. Ostensibly due to their resistance to exonucleases, circRNAs are known to be exceptionally stable. Previous work in Drosophila and mice have shown that circRNAs increase during aging in neural tissues. RESULTS: Here, we examined the global profile of circRNAs in C. elegans during aging by performing ribo-depleted total RNA-seq from the fourth larval stage (L4) through 10-day old adults. Using stringent bioinformatic criteria and experimental validation, we annotated a high-confidence set of 1166 circRNAs, including 575 newly discovered circRNAs. These circRNAs were derived from 797 genes with diverse functions, including genes involved in the determination of lifespan. A massive accumulation of circRNAs during aging was uncovered. Many hundreds of circRNAs were significantly increased among the aging time-points and increases of select circRNAs by over 40-fold during aging were quantified by RT-qPCR. The expression of 459 circRNAs was determined to be distinct from the expression of linear RNAs from the same host genes, demonstrating host gene independence of circRNA age-accumulation. CONCLUSIONS: We attribute the global scale of circRNA age-accumulation to the high composition of post-mitotic cells in adult C. elegans, coupled with the high resistance of circRNAs to decay. These findings suggest that the exceptional stability of circRNAs might explain age-accumulation trends observed from neural tissues of other organisms, which also have a high composition of post-mitotic cells. Given the suitability of C. elegans for aging research, it is now poised as an excellent model system to determine whether there are functional consequences of circRNA accumulation during aging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4386-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-03 /pmc/articles/PMC5753478/ /pubmed/29298683 http://dx.doi.org/10.1186/s12864-017-4386-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Cortés-López, Mariela Gruner, Matthew R. Cooper, Daphne A. Gruner, Hannah N. Voda, Alexandru-Ioan van der Linden, Alexander M. Miura, Pedro Global accumulation of circRNAs during aging in Caenorhabditis elegans |
title | Global accumulation of circRNAs during aging in Caenorhabditis elegans |
title_full | Global accumulation of circRNAs during aging in Caenorhabditis elegans |
title_fullStr | Global accumulation of circRNAs during aging in Caenorhabditis elegans |
title_full_unstemmed | Global accumulation of circRNAs during aging in Caenorhabditis elegans |
title_short | Global accumulation of circRNAs during aging in Caenorhabditis elegans |
title_sort | global accumulation of circrnas during aging in caenorhabditis elegans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753478/ https://www.ncbi.nlm.nih.gov/pubmed/29298683 http://dx.doi.org/10.1186/s12864-017-4386-y |
work_keys_str_mv | AT corteslopezmariela globalaccumulationofcircrnasduringagingincaenorhabditiselegans AT grunermatthewr globalaccumulationofcircrnasduringagingincaenorhabditiselegans AT cooperdaphnea globalaccumulationofcircrnasduringagingincaenorhabditiselegans AT grunerhannahn globalaccumulationofcircrnasduringagingincaenorhabditiselegans AT vodaalexandruioan globalaccumulationofcircrnasduringagingincaenorhabditiselegans AT vanderlindenalexanderm globalaccumulationofcircrnasduringagingincaenorhabditiselegans AT miurapedro globalaccumulationofcircrnasduringagingincaenorhabditiselegans |