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Reading the Evolution of Compartmentalization in the Ribosome Assembly Toolbox: The YRG Protein Family
Reconstructing the transition from a single compartment bacterium to a highly compartmentalized eukaryotic cell is one of the most studied problems of evolutionary cell biology. However, timing and details of the establishment of compartmentalization are unclear and difficult to assess. Here, we pro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224878/ https://www.ncbi.nlm.nih.gov/pubmed/28072865 http://dx.doi.org/10.1371/journal.pone.0169750 |
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author | Mier, Pablo Pérez-Pulido, Antonio J. Reynaud, Emmanuel G. Andrade-Navarro, Miguel A. |
author_facet | Mier, Pablo Pérez-Pulido, Antonio J. Reynaud, Emmanuel G. Andrade-Navarro, Miguel A. |
author_sort | Mier, Pablo |
collection | PubMed |
description | Reconstructing the transition from a single compartment bacterium to a highly compartmentalized eukaryotic cell is one of the most studied problems of evolutionary cell biology. However, timing and details of the establishment of compartmentalization are unclear and difficult to assess. Here, we propose the use of molecular markers specific to cellular compartments to set up a framework to advance the understanding of this complex intracellular process. Specifically, we use a protein family related to ribosome biogenesis, YRG (YlqF related GTPases), whose evolution is linked to the establishment of cellular compartments, leveraging the current genomic data. We analyzed orthologous proteins of the YRG family in a set of 171 proteomes for a total of 370 proteins. We identified ten YRG protein subfamilies that can be associated to six subcellular compartments (nuclear bodies, nucleolus, nucleus, cytosol, mitochondria, and chloroplast), and which were found in archaeal, bacterial and eukaryotic proteomes. Our analysis reveals organism streamlining related events in specific taxonomic groups such as Fungi. We conclude that the YRG family could be used as a compartmentalization marker, which could help to trace the evolutionary path relating cellular compartments with ribosome biogenesis. |
format | Online Article Text |
id | pubmed-5224878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-52248782017-01-31 Reading the Evolution of Compartmentalization in the Ribosome Assembly Toolbox: The YRG Protein Family Mier, Pablo Pérez-Pulido, Antonio J. Reynaud, Emmanuel G. Andrade-Navarro, Miguel A. PLoS One Research Article Reconstructing the transition from a single compartment bacterium to a highly compartmentalized eukaryotic cell is one of the most studied problems of evolutionary cell biology. However, timing and details of the establishment of compartmentalization are unclear and difficult to assess. Here, we propose the use of molecular markers specific to cellular compartments to set up a framework to advance the understanding of this complex intracellular process. Specifically, we use a protein family related to ribosome biogenesis, YRG (YlqF related GTPases), whose evolution is linked to the establishment of cellular compartments, leveraging the current genomic data. We analyzed orthologous proteins of the YRG family in a set of 171 proteomes for a total of 370 proteins. We identified ten YRG protein subfamilies that can be associated to six subcellular compartments (nuclear bodies, nucleolus, nucleus, cytosol, mitochondria, and chloroplast), and which were found in archaeal, bacterial and eukaryotic proteomes. Our analysis reveals organism streamlining related events in specific taxonomic groups such as Fungi. We conclude that the YRG family could be used as a compartmentalization marker, which could help to trace the evolutionary path relating cellular compartments with ribosome biogenesis. Public Library of Science 2017-01-10 /pmc/articles/PMC5224878/ /pubmed/28072865 http://dx.doi.org/10.1371/journal.pone.0169750 Text en © 2017 Mier et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Mier, Pablo Pérez-Pulido, Antonio J. Reynaud, Emmanuel G. Andrade-Navarro, Miguel A. Reading the Evolution of Compartmentalization in the Ribosome Assembly Toolbox: The YRG Protein Family |
title | Reading the Evolution of Compartmentalization in the Ribosome Assembly Toolbox: The YRG Protein Family |
title_full | Reading the Evolution of Compartmentalization in the Ribosome Assembly Toolbox: The YRG Protein Family |
title_fullStr | Reading the Evolution of Compartmentalization in the Ribosome Assembly Toolbox: The YRG Protein Family |
title_full_unstemmed | Reading the Evolution of Compartmentalization in the Ribosome Assembly Toolbox: The YRG Protein Family |
title_short | Reading the Evolution of Compartmentalization in the Ribosome Assembly Toolbox: The YRG Protein Family |
title_sort | reading the evolution of compartmentalization in the ribosome assembly toolbox: the yrg protein family |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224878/ https://www.ncbi.nlm.nih.gov/pubmed/28072865 http://dx.doi.org/10.1371/journal.pone.0169750 |
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