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Conserved and highly expressed tRNA derived fragments in zebrafish
BACKGROUND: Small non-coding RNAs (sncRNAs) are a class of transcripts implicated in several eukaryotic regulatory mechanisms, namely gene silencing and chromatin regulation. Despite significant progress in their identification by next generation sequencing (NGS) we are still far from understanding...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4688932/ https://www.ncbi.nlm.nih.gov/pubmed/26694924 http://dx.doi.org/10.1186/s12867-015-0050-8 |
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author | Soares, Ana Raquel Fernandes, Noémia Reverendo, Marisa Araújo, Hugo Rafael Oliveira, José Luís Moura, Gabriela M. R. Santos, Manuel A. S. |
author_facet | Soares, Ana Raquel Fernandes, Noémia Reverendo, Marisa Araújo, Hugo Rafael Oliveira, José Luís Moura, Gabriela M. R. Santos, Manuel A. S. |
author_sort | Soares, Ana Raquel |
collection | PubMed |
description | BACKGROUND: Small non-coding RNAs (sncRNAs) are a class of transcripts implicated in several eukaryotic regulatory mechanisms, namely gene silencing and chromatin regulation. Despite significant progress in their identification by next generation sequencing (NGS) we are still far from understanding their full diversity and functional repertoire. RESULTS: Here we report the identification of tRNA derived fragments (tRFs) by NGS of the sncRNA fraction of zebrafish. The tRFs identified are 18–30 nt long, are derived from specific 5′ and 3′ processing of mature tRNAs and are differentially expressed during development and in differentiated tissues, suggesting that they are likely produced by specific processing rather than random degradation of tRNAs. We further show that a highly expressed tRF (5′tRF-Pro(CGG)) is cleaved in vitro by Dicer and has silencing ability, indicating that it can enter the RNAi pathway. A computational analysis of zebrafish tRFs shows that they are conserved among vertebrates and mining of publicly available datasets reveals that some 5′tRFs are differentially expressed in disease conditions, namely during infection and colorectal cancer. CONCLUSIONS: tRFs constitute a class of conserved regulatory RNAs in vertebrates and may be involved in mechanisms of genome regulation and in some diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12867-015-0050-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4688932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46889322015-12-24 Conserved and highly expressed tRNA derived fragments in zebrafish Soares, Ana Raquel Fernandes, Noémia Reverendo, Marisa Araújo, Hugo Rafael Oliveira, José Luís Moura, Gabriela M. R. Santos, Manuel A. S. BMC Mol Biol Research Article BACKGROUND: Small non-coding RNAs (sncRNAs) are a class of transcripts implicated in several eukaryotic regulatory mechanisms, namely gene silencing and chromatin regulation. Despite significant progress in their identification by next generation sequencing (NGS) we are still far from understanding their full diversity and functional repertoire. RESULTS: Here we report the identification of tRNA derived fragments (tRFs) by NGS of the sncRNA fraction of zebrafish. The tRFs identified are 18–30 nt long, are derived from specific 5′ and 3′ processing of mature tRNAs and are differentially expressed during development and in differentiated tissues, suggesting that they are likely produced by specific processing rather than random degradation of tRNAs. We further show that a highly expressed tRF (5′tRF-Pro(CGG)) is cleaved in vitro by Dicer and has silencing ability, indicating that it can enter the RNAi pathway. A computational analysis of zebrafish tRFs shows that they are conserved among vertebrates and mining of publicly available datasets reveals that some 5′tRFs are differentially expressed in disease conditions, namely during infection and colorectal cancer. CONCLUSIONS: tRFs constitute a class of conserved regulatory RNAs in vertebrates and may be involved in mechanisms of genome regulation and in some diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12867-015-0050-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-22 /pmc/articles/PMC4688932/ /pubmed/26694924 http://dx.doi.org/10.1186/s12867-015-0050-8 Text en © Soares et al. 2015 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 Soares, Ana Raquel Fernandes, Noémia Reverendo, Marisa Araújo, Hugo Rafael Oliveira, José Luís Moura, Gabriela M. R. Santos, Manuel A. S. Conserved and highly expressed tRNA derived fragments in zebrafish |
title | Conserved and highly expressed tRNA derived fragments in zebrafish |
title_full | Conserved and highly expressed tRNA derived fragments in zebrafish |
title_fullStr | Conserved and highly expressed tRNA derived fragments in zebrafish |
title_full_unstemmed | Conserved and highly expressed tRNA derived fragments in zebrafish |
title_short | Conserved and highly expressed tRNA derived fragments in zebrafish |
title_sort | conserved and highly expressed trna derived fragments in zebrafish |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4688932/ https://www.ncbi.nlm.nih.gov/pubmed/26694924 http://dx.doi.org/10.1186/s12867-015-0050-8 |
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