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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....

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Autores principales: Cortés-López, Mariela, Gruner, Matthew R., Cooper, Daphne A., Gruner, Hannah N., Voda, Alexandru-Ioan, van der Linden, Alexander M., Miura, Pedro
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
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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.
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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
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