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Identification of functional long non-coding RNAs in C. elegans

BACKGROUND: Functional characterisation of the compact genome of the model organism Caenorhabditis elegans remains incomplete despite its sequencing 20 years ago. The last decade of research has seen a tremendous increase in the number of non-coding RNAs identified in various organisms. While we hav...

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Autores principales: Akay, Alper, Jordan, David, Navarro, Isabela Cunha, Wrzesinski, Tomasz, Ponting, Chris P., Miska, Eric A., Haerty, Wilfried
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378714/
https://www.ncbi.nlm.nih.gov/pubmed/30777050
http://dx.doi.org/10.1186/s12915-019-0635-7
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author Akay, Alper
Jordan, David
Navarro, Isabela Cunha
Wrzesinski, Tomasz
Ponting, Chris P.
Miska, Eric A.
Haerty, Wilfried
author_facet Akay, Alper
Jordan, David
Navarro, Isabela Cunha
Wrzesinski, Tomasz
Ponting, Chris P.
Miska, Eric A.
Haerty, Wilfried
author_sort Akay, Alper
collection PubMed
description BACKGROUND: Functional characterisation of the compact genome of the model organism Caenorhabditis elegans remains incomplete despite its sequencing 20 years ago. The last decade of research has seen a tremendous increase in the number of non-coding RNAs identified in various organisms. While we have mechanistic understandings of small non-coding RNA pathways, long non-coding RNAs represent a diverse class of active transcripts whose function remains less well characterised. RESULTS: By analysing hundreds of published transcriptome datasets, we annotated 3392 potential lncRNAs including 143 multi-exonic loci that showed increased nucleotide conservation and GC content relative to other non-coding regions. Using CRISPR/Cas9 genome editing, we generated deletion mutants for ten long non-coding RNA loci. Using automated microscopy for in-depth phenotyping, we show that six of the long non-coding RNA loci are required for normal development and fertility. Using RNA interference-mediated gene knock-down, we provide evidence that for two of the long non-coding RNA loci, the observed phenotypes are dependent on the corresponding RNA transcripts. CONCLUSIONS: Our results highlight that a large section of the non-coding regions of the C. elegans genome remains unexplored. Based on our in vivo analysis of a selection of high-confidence lncRNA loci, we expect that a significant proportion of these high-confidence regions is likely to have a biological function at either the genomic or the transcript level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0635-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-63787142019-02-28 Identification of functional long non-coding RNAs in C. elegans Akay, Alper Jordan, David Navarro, Isabela Cunha Wrzesinski, Tomasz Ponting, Chris P. Miska, Eric A. Haerty, Wilfried BMC Biol Research Article BACKGROUND: Functional characterisation of the compact genome of the model organism Caenorhabditis elegans remains incomplete despite its sequencing 20 years ago. The last decade of research has seen a tremendous increase in the number of non-coding RNAs identified in various organisms. While we have mechanistic understandings of small non-coding RNA pathways, long non-coding RNAs represent a diverse class of active transcripts whose function remains less well characterised. RESULTS: By analysing hundreds of published transcriptome datasets, we annotated 3392 potential lncRNAs including 143 multi-exonic loci that showed increased nucleotide conservation and GC content relative to other non-coding regions. Using CRISPR/Cas9 genome editing, we generated deletion mutants for ten long non-coding RNA loci. Using automated microscopy for in-depth phenotyping, we show that six of the long non-coding RNA loci are required for normal development and fertility. Using RNA interference-mediated gene knock-down, we provide evidence that for two of the long non-coding RNA loci, the observed phenotypes are dependent on the corresponding RNA transcripts. CONCLUSIONS: Our results highlight that a large section of the non-coding regions of the C. elegans genome remains unexplored. Based on our in vivo analysis of a selection of high-confidence lncRNA loci, we expect that a significant proportion of these high-confidence regions is likely to have a biological function at either the genomic or the transcript level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0635-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-18 /pmc/articles/PMC6378714/ /pubmed/30777050 http://dx.doi.org/10.1186/s12915-019-0635-7 Text en © The Author(s). 2019 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
Akay, Alper
Jordan, David
Navarro, Isabela Cunha
Wrzesinski, Tomasz
Ponting, Chris P.
Miska, Eric A.
Haerty, Wilfried
Identification of functional long non-coding RNAs in C. elegans
title Identification of functional long non-coding RNAs in C. elegans
title_full Identification of functional long non-coding RNAs in C. elegans
title_fullStr Identification of functional long non-coding RNAs in C. elegans
title_full_unstemmed Identification of functional long non-coding RNAs in C. elegans
title_short Identification of functional long non-coding RNAs in C. elegans
title_sort identification of functional long non-coding rnas in c. elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6378714/
https://www.ncbi.nlm.nih.gov/pubmed/30777050
http://dx.doi.org/10.1186/s12915-019-0635-7
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