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Ancient gene duplications have shaped developmental stage-specific expression in Pristionchus pacificus

BACKGROUND: The development of multicellular organisms is accompanied by gene expression changes in differentiating cells. Profiling stage-specific expression during development may reveal important insights into gene sets that contributed to the morphological diversity across the animal kingdom. RE...

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Autores principales: Baskaran, Praveen, Rödelsperger, Christian, Prabh, Neel, Serobyan, Vahan, Markov, Gabriel V., Hirsekorn, Antje, Dieterich, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570658/
https://www.ncbi.nlm.nih.gov/pubmed/26370559
http://dx.doi.org/10.1186/s12862-015-0466-2
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author Baskaran, Praveen
Rödelsperger, Christian
Prabh, Neel
Serobyan, Vahan
Markov, Gabriel V.
Hirsekorn, Antje
Dieterich, Christoph
author_facet Baskaran, Praveen
Rödelsperger, Christian
Prabh, Neel
Serobyan, Vahan
Markov, Gabriel V.
Hirsekorn, Antje
Dieterich, Christoph
author_sort Baskaran, Praveen
collection PubMed
description BACKGROUND: The development of multicellular organisms is accompanied by gene expression changes in differentiating cells. Profiling stage-specific expression during development may reveal important insights into gene sets that contributed to the morphological diversity across the animal kingdom. RESULTS: We sequenced RNA-seq libraries throughout a developmental timecourse of the nematode Pristionchus pacificus. The transcriptomes reflect early larval stages, adult worms including late larvae, and growth-arrested dauer larvae and allowed the identification of developmentally regulated gene clusters. Our data reveals similar trends as previous transcriptome profiling of dauer worms and represents the first expression data for early larvae in P. pacificus. Gene expression clusters characterizing early larval stages show most significant enrichments of chaperones, while collagens are most significantly enriched in transcriptomes of late larvae and adult worms. By combining expression data with phylogenetic analysis, we found that developmentally regulated genes are found in paralogous clusters that have arisen through lineage-specific duplications after the split from the Caenorhabditis elegans branch. CONCLUSIONS: We propose that gene duplications of developmentally regulated genes represent a plausible evolutionary mechanism to increase the dosage of stage-specific expression. Consequently, this may contribute to the substantial divergence in expression profiles that has been observed across larger evolutionary time scales. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0466-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-45706582015-09-16 Ancient gene duplications have shaped developmental stage-specific expression in Pristionchus pacificus Baskaran, Praveen Rödelsperger, Christian Prabh, Neel Serobyan, Vahan Markov, Gabriel V. Hirsekorn, Antje Dieterich, Christoph BMC Evol Biol Research Article BACKGROUND: The development of multicellular organisms is accompanied by gene expression changes in differentiating cells. Profiling stage-specific expression during development may reveal important insights into gene sets that contributed to the morphological diversity across the animal kingdom. RESULTS: We sequenced RNA-seq libraries throughout a developmental timecourse of the nematode Pristionchus pacificus. The transcriptomes reflect early larval stages, adult worms including late larvae, and growth-arrested dauer larvae and allowed the identification of developmentally regulated gene clusters. Our data reveals similar trends as previous transcriptome profiling of dauer worms and represents the first expression data for early larvae in P. pacificus. Gene expression clusters characterizing early larval stages show most significant enrichments of chaperones, while collagens are most significantly enriched in transcriptomes of late larvae and adult worms. By combining expression data with phylogenetic analysis, we found that developmentally regulated genes are found in paralogous clusters that have arisen through lineage-specific duplications after the split from the Caenorhabditis elegans branch. CONCLUSIONS: We propose that gene duplications of developmentally regulated genes represent a plausible evolutionary mechanism to increase the dosage of stage-specific expression. Consequently, this may contribute to the substantial divergence in expression profiles that has been observed across larger evolutionary time scales. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0466-2) contains supplementary material, which is available to authorized users. BioMed Central 2015-09-15 /pmc/articles/PMC4570658/ /pubmed/26370559 http://dx.doi.org/10.1186/s12862-015-0466-2 Text en © Baskaran et al. 2015 Open Access This 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
Baskaran, Praveen
Rödelsperger, Christian
Prabh, Neel
Serobyan, Vahan
Markov, Gabriel V.
Hirsekorn, Antje
Dieterich, Christoph
Ancient gene duplications have shaped developmental stage-specific expression in Pristionchus pacificus
title Ancient gene duplications have shaped developmental stage-specific expression in Pristionchus pacificus
title_full Ancient gene duplications have shaped developmental stage-specific expression in Pristionchus pacificus
title_fullStr Ancient gene duplications have shaped developmental stage-specific expression in Pristionchus pacificus
title_full_unstemmed Ancient gene duplications have shaped developmental stage-specific expression in Pristionchus pacificus
title_short Ancient gene duplications have shaped developmental stage-specific expression in Pristionchus pacificus
title_sort ancient gene duplications have shaped developmental stage-specific expression in pristionchus pacificus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4570658/
https://www.ncbi.nlm.nih.gov/pubmed/26370559
http://dx.doi.org/10.1186/s12862-015-0466-2
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