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The Capsaspora genome reveals a complex unicellular prehistory of animals
To reconstruct the evolutionary origin of multicellular animals from their unicellular ancestors, the genome sequences of diverse unicellular relatives are essential. However, only the genome of the choanoflagellate Monosiga brevicollis has been reported to date. Here we completely sequence the geno...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753549/ https://www.ncbi.nlm.nih.gov/pubmed/23942320 http://dx.doi.org/10.1038/ncomms3325 |
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author | Suga, Hiroshi Chen, Zehua de Mendoza, Alex Sebé-Pedrós, Arnau Brown, Matthew W. Kramer, Eric Carr, Martin Kerner, Pierre Vervoort, Michel Sánchez-Pons, Núria Torruella, Guifré Derelle, Romain Manning, Gerard Lang, B. Franz Russ, Carsten Haas, Brian J. Roger, Andrew J. Nusbaum, Chad Ruiz-Trillo, Iñaki |
author_facet | Suga, Hiroshi Chen, Zehua de Mendoza, Alex Sebé-Pedrós, Arnau Brown, Matthew W. Kramer, Eric Carr, Martin Kerner, Pierre Vervoort, Michel Sánchez-Pons, Núria Torruella, Guifré Derelle, Romain Manning, Gerard Lang, B. Franz Russ, Carsten Haas, Brian J. Roger, Andrew J. Nusbaum, Chad Ruiz-Trillo, Iñaki |
author_sort | Suga, Hiroshi |
collection | PubMed |
description | To reconstruct the evolutionary origin of multicellular animals from their unicellular ancestors, the genome sequences of diverse unicellular relatives are essential. However, only the genome of the choanoflagellate Monosiga brevicollis has been reported to date. Here we completely sequence the genome of the filasterean Capsaspora owczarzaki, the closest known unicellular relative of metazoans besides choanoflagellates. Analyses of this genome alter our understanding of the molecular complexity of metazoans’ unicellular ancestors showing that they had a richer repertoire of proteins involved in cell adhesion and transcriptional regulation than previously inferred only with the choanoflagellate genome. Some of these proteins were secondarily lost in choanoflagellates. In contrast, most intercellular signalling systems controlling development evolved later concomitant with the emergence of the first metazoans. We propose that the acquisition of these metazoan-specific developmental systems and the co-option of pre-existing genes drove the evolutionary transition from unicellular protists to metazoans. |
format | Online Article Text |
id | pubmed-3753549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-37535492013-08-27 The Capsaspora genome reveals a complex unicellular prehistory of animals Suga, Hiroshi Chen, Zehua de Mendoza, Alex Sebé-Pedrós, Arnau Brown, Matthew W. Kramer, Eric Carr, Martin Kerner, Pierre Vervoort, Michel Sánchez-Pons, Núria Torruella, Guifré Derelle, Romain Manning, Gerard Lang, B. Franz Russ, Carsten Haas, Brian J. Roger, Andrew J. Nusbaum, Chad Ruiz-Trillo, Iñaki Nat Commun Article To reconstruct the evolutionary origin of multicellular animals from their unicellular ancestors, the genome sequences of diverse unicellular relatives are essential. However, only the genome of the choanoflagellate Monosiga brevicollis has been reported to date. Here we completely sequence the genome of the filasterean Capsaspora owczarzaki, the closest known unicellular relative of metazoans besides choanoflagellates. Analyses of this genome alter our understanding of the molecular complexity of metazoans’ unicellular ancestors showing that they had a richer repertoire of proteins involved in cell adhesion and transcriptional regulation than previously inferred only with the choanoflagellate genome. Some of these proteins were secondarily lost in choanoflagellates. In contrast, most intercellular signalling systems controlling development evolved later concomitant with the emergence of the first metazoans. We propose that the acquisition of these metazoan-specific developmental systems and the co-option of pre-existing genes drove the evolutionary transition from unicellular protists to metazoans. Nature Pub. Group 2013-08-14 /pmc/articles/PMC3753549/ /pubmed/23942320 http://dx.doi.org/10.1038/ncomms3325 Text en Copyright © 2013, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Article Suga, Hiroshi Chen, Zehua de Mendoza, Alex Sebé-Pedrós, Arnau Brown, Matthew W. Kramer, Eric Carr, Martin Kerner, Pierre Vervoort, Michel Sánchez-Pons, Núria Torruella, Guifré Derelle, Romain Manning, Gerard Lang, B. Franz Russ, Carsten Haas, Brian J. Roger, Andrew J. Nusbaum, Chad Ruiz-Trillo, Iñaki The Capsaspora genome reveals a complex unicellular prehistory of animals |
title | The Capsaspora genome reveals a complex unicellular prehistory of animals |
title_full | The Capsaspora genome reveals a complex unicellular prehistory of animals |
title_fullStr | The Capsaspora genome reveals a complex unicellular prehistory of animals |
title_full_unstemmed | The Capsaspora genome reveals a complex unicellular prehistory of animals |
title_short | The Capsaspora genome reveals a complex unicellular prehistory of animals |
title_sort | capsaspora genome reveals a complex unicellular prehistory of animals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753549/ https://www.ncbi.nlm.nih.gov/pubmed/23942320 http://dx.doi.org/10.1038/ncomms3325 |
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