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Comparative Expression Dynamics of Intergenic Long Noncoding RNAs in the Genus Drosophila
Thousands of long noncoding RNAs (lncRNAs) have been annotated in eukaryotic genomes, but comparative transcriptomic approaches are necessary to understand their biological impact and evolution. To facilitate such comparative studies in Drosophila, we identified and characterized lncRNAs in a second...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943187/ https://www.ncbi.nlm.nih.gov/pubmed/27189981 http://dx.doi.org/10.1093/gbe/evw116 |
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author | Nyberg, Kevin G. Machado, Carlos A. |
author_facet | Nyberg, Kevin G. Machado, Carlos A. |
author_sort | Nyberg, Kevin G. |
collection | PubMed |
description | Thousands of long noncoding RNAs (lncRNAs) have been annotated in eukaryotic genomes, but comparative transcriptomic approaches are necessary to understand their biological impact and evolution. To facilitate such comparative studies in Drosophila, we identified and characterized lncRNAs in a second Drosophilid—the evolutionary model Drosophila pseudoobscura. Using RNA-Seq and computational filtering of protein-coding potential, we identified 1,589 intergenic lncRNA loci in D. pseudoobscura. We surveyed multiple sex-specific developmental stages and found, like in Drosophila melanogaster, increasingly prolific lncRNA expression through male development and an overrepresentation of lncRNAs in the testes. Other trends seen in D. melanogaster, like reduced pupal expression, were not observed. Nonrandom distributions of female-biased and non-testis-specific male-biased lncRNAs between the X chromosome and autosomes are consistent with selection-based models of gene trafficking to optimize genomic location of sex-biased genes. The numerous testis-specific lncRNAs, however, are randomly distributed between the X and autosomes, and we cannot reject the hypothesis that many of these are likely to be spurious transcripts. Finally, using annotated lncRNAs in both species, we identified 134 putative lncRNA homologs between D. pseudoobscura and D. melanogaster and find that many have conserved developmental expression dynamics, making them ideal candidates for future functional analyses. |
format | Online Article Text |
id | pubmed-4943187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49431872016-07-14 Comparative Expression Dynamics of Intergenic Long Noncoding RNAs in the Genus Drosophila Nyberg, Kevin G. Machado, Carlos A. Genome Biol Evol Research Article Thousands of long noncoding RNAs (lncRNAs) have been annotated in eukaryotic genomes, but comparative transcriptomic approaches are necessary to understand their biological impact and evolution. To facilitate such comparative studies in Drosophila, we identified and characterized lncRNAs in a second Drosophilid—the evolutionary model Drosophila pseudoobscura. Using RNA-Seq and computational filtering of protein-coding potential, we identified 1,589 intergenic lncRNA loci in D. pseudoobscura. We surveyed multiple sex-specific developmental stages and found, like in Drosophila melanogaster, increasingly prolific lncRNA expression through male development and an overrepresentation of lncRNAs in the testes. Other trends seen in D. melanogaster, like reduced pupal expression, were not observed. Nonrandom distributions of female-biased and non-testis-specific male-biased lncRNAs between the X chromosome and autosomes are consistent with selection-based models of gene trafficking to optimize genomic location of sex-biased genes. The numerous testis-specific lncRNAs, however, are randomly distributed between the X and autosomes, and we cannot reject the hypothesis that many of these are likely to be spurious transcripts. Finally, using annotated lncRNAs in both species, we identified 134 putative lncRNA homologs between D. pseudoobscura and D. melanogaster and find that many have conserved developmental expression dynamics, making them ideal candidates for future functional analyses. Oxford University Press 2016-05-18 /pmc/articles/PMC4943187/ /pubmed/27189981 http://dx.doi.org/10.1093/gbe/evw116 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Nyberg, Kevin G. Machado, Carlos A. Comparative Expression Dynamics of Intergenic Long Noncoding RNAs in the Genus Drosophila |
title | Comparative Expression Dynamics of Intergenic Long Noncoding RNAs in the Genus Drosophila |
title_full | Comparative Expression Dynamics of Intergenic Long Noncoding RNAs in the Genus Drosophila |
title_fullStr | Comparative Expression Dynamics of Intergenic Long Noncoding RNAs in the Genus Drosophila |
title_full_unstemmed | Comparative Expression Dynamics of Intergenic Long Noncoding RNAs in the Genus Drosophila |
title_short | Comparative Expression Dynamics of Intergenic Long Noncoding RNAs in the Genus Drosophila |
title_sort | comparative expression dynamics of intergenic long noncoding rnas in the genus drosophila |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943187/ https://www.ncbi.nlm.nih.gov/pubmed/27189981 http://dx.doi.org/10.1093/gbe/evw116 |
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