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Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis

BACKGROUND: Membrane-bound organelles are a defining feature of eukaryotic cells, and play a central role in most of their fundamental processes. The Rab G proteins are the single largest family of proteins that participate in the traffic between organelles, with 66 Rabs encoded in the human genome....

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Autores principales: Klöpper, Tobias H, Kienle, Nickias, Fasshauer, Dirk, Munro, Sean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425129/
https://www.ncbi.nlm.nih.gov/pubmed/22873208
http://dx.doi.org/10.1186/1741-7007-10-71
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author Klöpper, Tobias H
Kienle, Nickias
Fasshauer, Dirk
Munro, Sean
author_facet Klöpper, Tobias H
Kienle, Nickias
Fasshauer, Dirk
Munro, Sean
author_sort Klöpper, Tobias H
collection PubMed
description BACKGROUND: Membrane-bound organelles are a defining feature of eukaryotic cells, and play a central role in most of their fundamental processes. The Rab G proteins are the single largest family of proteins that participate in the traffic between organelles, with 66 Rabs encoded in the human genome. Rabs direct the organelle-specific recruitment of vesicle tethering factors, motor proteins, and regulators of membrane traffic. Each organelle or vesicle class is typically associated with one or more Rab, with the Rabs present in a particular cell reflecting that cell's complement of organelles and trafficking routes. RESULTS: Through iterative use of hidden Markov models and tree building, we classified Rabs across the eukaryotic kingdom to provide the most comprehensive view of Rab evolution obtained to date. A strikingly large repertoire of at least 20 Rabs appears to have been present in the last eukaryotic common ancestor (LECA), consistent with the 'complexity early' view of eukaryotic evolution. We were able to place these Rabs into six supergroups, giving a deep view into eukaryotic prehistory. CONCLUSIONS: Tracing the fate of the LECA Rabs revealed extensive losses with many extant eukaryotes having fewer Rabs, and none having the full complement. We found that other Rabs have expanded and diversified, including a large expansion at the dawn of metazoans, which could be followed to provide an account of the evolutionary history of all human Rabs. Some Rab changes could be correlated with differences in cellular organization, and the relative lack of variation in other families of membrane-traffic proteins suggests that it is the changes in Rabs that primarily underlies the variation in organelles between species and cell types.
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spelling pubmed-34251292012-08-23 Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis Klöpper, Tobias H Kienle, Nickias Fasshauer, Dirk Munro, Sean BMC Biol Research Article BACKGROUND: Membrane-bound organelles are a defining feature of eukaryotic cells, and play a central role in most of their fundamental processes. The Rab G proteins are the single largest family of proteins that participate in the traffic between organelles, with 66 Rabs encoded in the human genome. Rabs direct the organelle-specific recruitment of vesicle tethering factors, motor proteins, and regulators of membrane traffic. Each organelle or vesicle class is typically associated with one or more Rab, with the Rabs present in a particular cell reflecting that cell's complement of organelles and trafficking routes. RESULTS: Through iterative use of hidden Markov models and tree building, we classified Rabs across the eukaryotic kingdom to provide the most comprehensive view of Rab evolution obtained to date. A strikingly large repertoire of at least 20 Rabs appears to have been present in the last eukaryotic common ancestor (LECA), consistent with the 'complexity early' view of eukaryotic evolution. We were able to place these Rabs into six supergroups, giving a deep view into eukaryotic prehistory. CONCLUSIONS: Tracing the fate of the LECA Rabs revealed extensive losses with many extant eukaryotes having fewer Rabs, and none having the full complement. We found that other Rabs have expanded and diversified, including a large expansion at the dawn of metazoans, which could be followed to provide an account of the evolutionary history of all human Rabs. Some Rab changes could be correlated with differences in cellular organization, and the relative lack of variation in other families of membrane-traffic proteins suggests that it is the changes in Rabs that primarily underlies the variation in organelles between species and cell types. BioMed Central 2012-08-08 /pmc/articles/PMC3425129/ /pubmed/22873208 http://dx.doi.org/10.1186/1741-7007-10-71 Text en Copyright ©2012 Klöpper et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Klöpper, Tobias H
Kienle, Nickias
Fasshauer, Dirk
Munro, Sean
Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis
title Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis
title_full Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis
title_fullStr Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis
title_full_unstemmed Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis
title_short Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis
title_sort untangling the evolution of rab g proteins: implications of a comprehensive genomic analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3425129/
https://www.ncbi.nlm.nih.gov/pubmed/22873208
http://dx.doi.org/10.1186/1741-7007-10-71
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