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Myosin repertoire expansion coincides with eukaryotic diversification in the Mesoproterozoic era
BACKGROUND: The last eukaryotic common ancestor already had an amazingly complex cell possessing genomic and cellular features such as spliceosomal introns, mitochondria, cilia-dependent motility, and a cytoskeleton together with several intracellular transport systems. In contrast to the microtubul...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583752/ https://www.ncbi.nlm.nih.gov/pubmed/28870165 http://dx.doi.org/10.1186/s12862-017-1056-2 |
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author | Kollmar, Martin Mühlhausen, Stefanie |
author_facet | Kollmar, Martin Mühlhausen, Stefanie |
author_sort | Kollmar, Martin |
collection | PubMed |
description | BACKGROUND: The last eukaryotic common ancestor already had an amazingly complex cell possessing genomic and cellular features such as spliceosomal introns, mitochondria, cilia-dependent motility, and a cytoskeleton together with several intracellular transport systems. In contrast to the microtubule-based dyneins and kinesins, the actin-filament associated myosins are considerably divergent in extant eukaryotes and a unifying picture of their evolution has not yet emerged. RESULTS: Here, we manually assembled and annotated 7852 myosins from 929 eukaryotes providing an unprecedented dense sequence and taxonomic sampling. For classification we complemented phylogenetic analyses with gene structure comparisons resulting in 79 distinct myosin classes. The intron pattern analysis and the taxonomic distribution of the classes suggest two myosins in the last eukaryotic common ancestor, a class-1 prototype and another myosin, which is most likely the ancestor of all other myosin classes. The sparse distribution of class-2 and class-4 myosins outside their major lineages contradicts their presence in the last eukaryotic common ancestor but instead strongly suggests early eukaryote-eukaryote horizontal gene transfer. CONCLUSIONS: By correlating the evolution of myosin diversity with the history of Earth we found that myosin innovation occurred in independent major “burst” events in the major eukaryotic lineages. Most myosin inventions happened in the Mesoproterozoic era. In the late Neoproterozoic era, a process of extensive independent myosin loss began simultaneously with further eukaryotic diversification. Since the Cambrian explosion, myosin repertoire expansion is driven by lineage- and species-specific gene and genome duplications leading to subfunctionalization and fine-tuning of myosin functions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-017-1056-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5583752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55837522017-09-06 Myosin repertoire expansion coincides with eukaryotic diversification in the Mesoproterozoic era Kollmar, Martin Mühlhausen, Stefanie BMC Evol Biol Research Article BACKGROUND: The last eukaryotic common ancestor already had an amazingly complex cell possessing genomic and cellular features such as spliceosomal introns, mitochondria, cilia-dependent motility, and a cytoskeleton together with several intracellular transport systems. In contrast to the microtubule-based dyneins and kinesins, the actin-filament associated myosins are considerably divergent in extant eukaryotes and a unifying picture of their evolution has not yet emerged. RESULTS: Here, we manually assembled and annotated 7852 myosins from 929 eukaryotes providing an unprecedented dense sequence and taxonomic sampling. For classification we complemented phylogenetic analyses with gene structure comparisons resulting in 79 distinct myosin classes. The intron pattern analysis and the taxonomic distribution of the classes suggest two myosins in the last eukaryotic common ancestor, a class-1 prototype and another myosin, which is most likely the ancestor of all other myosin classes. The sparse distribution of class-2 and class-4 myosins outside their major lineages contradicts their presence in the last eukaryotic common ancestor but instead strongly suggests early eukaryote-eukaryote horizontal gene transfer. CONCLUSIONS: By correlating the evolution of myosin diversity with the history of Earth we found that myosin innovation occurred in independent major “burst” events in the major eukaryotic lineages. Most myosin inventions happened in the Mesoproterozoic era. In the late Neoproterozoic era, a process of extensive independent myosin loss began simultaneously with further eukaryotic diversification. Since the Cambrian explosion, myosin repertoire expansion is driven by lineage- and species-specific gene and genome duplications leading to subfunctionalization and fine-tuning of myosin functions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-017-1056-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-04 /pmc/articles/PMC5583752/ /pubmed/28870165 http://dx.doi.org/10.1186/s12862-017-1056-2 Text en © The Author(s). 2017 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 Kollmar, Martin Mühlhausen, Stefanie Myosin repertoire expansion coincides with eukaryotic diversification in the Mesoproterozoic era |
title | Myosin repertoire expansion coincides with eukaryotic diversification in the Mesoproterozoic era |
title_full | Myosin repertoire expansion coincides with eukaryotic diversification in the Mesoproterozoic era |
title_fullStr | Myosin repertoire expansion coincides with eukaryotic diversification in the Mesoproterozoic era |
title_full_unstemmed | Myosin repertoire expansion coincides with eukaryotic diversification in the Mesoproterozoic era |
title_short | Myosin repertoire expansion coincides with eukaryotic diversification in the Mesoproterozoic era |
title_sort | myosin repertoire expansion coincides with eukaryotic diversification in the mesoproterozoic era |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583752/ https://www.ncbi.nlm.nih.gov/pubmed/28870165 http://dx.doi.org/10.1186/s12862-017-1056-2 |
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