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Complex transcriptional regulation and independent evolution of fungal-like traits in a relative of animals
Cell-type specification through differential genome regulation is a hallmark of complex multicellularity. However, it remains unclear how this process evolved during the transition from unicellular to multicellular organisms. To address this question, we investigated transcriptional dynamics in the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739763/ https://www.ncbi.nlm.nih.gov/pubmed/26465111 http://dx.doi.org/10.7554/eLife.08904 |
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author | de Mendoza, Alex Suga, Hiroshi Permanyer, Jon Irimia, Manuel Ruiz-Trillo, Iñaki |
author_facet | de Mendoza, Alex Suga, Hiroshi Permanyer, Jon Irimia, Manuel Ruiz-Trillo, Iñaki |
author_sort | de Mendoza, Alex |
collection | PubMed |
description | Cell-type specification through differential genome regulation is a hallmark of complex multicellularity. However, it remains unclear how this process evolved during the transition from unicellular to multicellular organisms. To address this question, we investigated transcriptional dynamics in the ichthyosporean Creolimax fragrantissima, a relative of animals that undergoes coenocytic development. We find that Creolimax utilizes dynamic regulation of alternative splicing, long inter-genic non-coding RNAs and co-regulated gene modules associated with animal multicellularity in a cell-type specific manner. Moreover, our study suggests that the different cell types of the three closest animal relatives (ichthyosporeans, filastereans and choanoflagellates) are the product of lineage-specific innovations. Additionally, a proteomic survey of the secretome reveals adaptations to a fungal-like lifestyle. In summary, the diversity of cell types among protistan relatives of animals and their complex genome regulation demonstrates that the last unicellular ancestor of animals was already capable of elaborate specification of cell types. DOI: http://dx.doi.org/10.7554/eLife.08904.001 |
format | Online Article Text |
id | pubmed-4739763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47397632016-02-04 Complex transcriptional regulation and independent evolution of fungal-like traits in a relative of animals de Mendoza, Alex Suga, Hiroshi Permanyer, Jon Irimia, Manuel Ruiz-Trillo, Iñaki eLife Developmental Biology and Stem Cells Cell-type specification through differential genome regulation is a hallmark of complex multicellularity. However, it remains unclear how this process evolved during the transition from unicellular to multicellular organisms. To address this question, we investigated transcriptional dynamics in the ichthyosporean Creolimax fragrantissima, a relative of animals that undergoes coenocytic development. We find that Creolimax utilizes dynamic regulation of alternative splicing, long inter-genic non-coding RNAs and co-regulated gene modules associated with animal multicellularity in a cell-type specific manner. Moreover, our study suggests that the different cell types of the three closest animal relatives (ichthyosporeans, filastereans and choanoflagellates) are the product of lineage-specific innovations. Additionally, a proteomic survey of the secretome reveals adaptations to a fungal-like lifestyle. In summary, the diversity of cell types among protistan relatives of animals and their complex genome regulation demonstrates that the last unicellular ancestor of animals was already capable of elaborate specification of cell types. DOI: http://dx.doi.org/10.7554/eLife.08904.001 eLife Sciences Publications, Ltd 2015-10-14 /pmc/articles/PMC4739763/ /pubmed/26465111 http://dx.doi.org/10.7554/eLife.08904 Text en © 2015, de Mendoza et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells de Mendoza, Alex Suga, Hiroshi Permanyer, Jon Irimia, Manuel Ruiz-Trillo, Iñaki Complex transcriptional regulation and independent evolution of fungal-like traits in a relative of animals |
title | Complex transcriptional regulation and independent evolution of fungal-like traits in a relative of animals |
title_full | Complex transcriptional regulation and independent evolution of fungal-like traits in a relative of animals |
title_fullStr | Complex transcriptional regulation and independent evolution of fungal-like traits in a relative of animals |
title_full_unstemmed | Complex transcriptional regulation and independent evolution of fungal-like traits in a relative of animals |
title_short | Complex transcriptional regulation and independent evolution of fungal-like traits in a relative of animals |
title_sort | complex transcriptional regulation and independent evolution of fungal-like traits in a relative of animals |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4739763/ https://www.ncbi.nlm.nih.gov/pubmed/26465111 http://dx.doi.org/10.7554/eLife.08904 |
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