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The frontier between cell and organelle: genome analysis of Candidatus Carsonella ruddii

BACKGROUND: Bacterial symbioses are widespread among insects. The early establishment of such symbiotic associations has probably been one of the key factors for the evolutionary success of insects, since it may have allowed access to novel ecological niches and to new imbalanced food resources, suc...

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Autores principales: Tamames, Javier, Gil, Rosario, Latorre, Amparo, Peretó, Juli, Silva, Francisco J, Moya, Andrés
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175510/
https://www.ncbi.nlm.nih.gov/pubmed/17908294
http://dx.doi.org/10.1186/1471-2148-7-181
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author Tamames, Javier
Gil, Rosario
Latorre, Amparo
Peretó, Juli
Silva, Francisco J
Moya, Andrés
author_facet Tamames, Javier
Gil, Rosario
Latorre, Amparo
Peretó, Juli
Silva, Francisco J
Moya, Andrés
author_sort Tamames, Javier
collection PubMed
description BACKGROUND: Bacterial symbioses are widespread among insects. The early establishment of such symbiotic associations has probably been one of the key factors for the evolutionary success of insects, since it may have allowed access to novel ecological niches and to new imbalanced food resources, such as plant sap or blood. Several genomes of bacterial endosymbionts of different insect species have been recently sequenced, and their biology has been extensively studied. Recently, the complete genome sequence of Candidatus Carsonella ruddii, considered the primary endosymbiont of the psyllid Pachpsylla venusta, has been published. This genome consists of a circular chromosome of 159,662 bp and has been proposed as the smallest bacterial endosymbiont genome known to date. RESULTS: The detailed analysis of the gene content of C. ruddii shows that the extensive degradation of the genome is not compatible with its consideration as a mutualistic endosymbiont and, even more, as a living organism. The ability to perform most essential functions for a cell to be considered alive is heavily impaired by the lack of genes involved in DNA replication, transcription and translation. Furthermore, the shortening of genes causes, in some cases, the loss of essential domains and functional residues needed to fulfill such vital functions. In addition, at least half of the pathways towards the biosynthesis of essential amino acids, its proposed symbiotic function, are completely or partially lost. CONCLUSION: We propose that this strain of C. ruddii can be viewed as a further step towards the degeneration of the former primary endosymbiont and its transformation in a subcellular new entity between living cells and organelles. Although the transition of genes from C. ruddii to the host nucleus has been proposed, the amount of genes that should have been transferred to the germinal line of the insect would be so big that it would be more plausible to consider the implication of the mitochondrial machinery encoded in the insect nucleus. Furthermore, since most genes for the biosynthesis of essential amino acids have also been lost, it is likely that the host depends on another yet unidentified symbiont to complement its deficient diet.
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spelling pubmed-21755102008-01-08 The frontier between cell and organelle: genome analysis of Candidatus Carsonella ruddii Tamames, Javier Gil, Rosario Latorre, Amparo Peretó, Juli Silva, Francisco J Moya, Andrés BMC Evol Biol Research Article BACKGROUND: Bacterial symbioses are widespread among insects. The early establishment of such symbiotic associations has probably been one of the key factors for the evolutionary success of insects, since it may have allowed access to novel ecological niches and to new imbalanced food resources, such as plant sap or blood. Several genomes of bacterial endosymbionts of different insect species have been recently sequenced, and their biology has been extensively studied. Recently, the complete genome sequence of Candidatus Carsonella ruddii, considered the primary endosymbiont of the psyllid Pachpsylla venusta, has been published. This genome consists of a circular chromosome of 159,662 bp and has been proposed as the smallest bacterial endosymbiont genome known to date. RESULTS: The detailed analysis of the gene content of C. ruddii shows that the extensive degradation of the genome is not compatible with its consideration as a mutualistic endosymbiont and, even more, as a living organism. The ability to perform most essential functions for a cell to be considered alive is heavily impaired by the lack of genes involved in DNA replication, transcription and translation. Furthermore, the shortening of genes causes, in some cases, the loss of essential domains and functional residues needed to fulfill such vital functions. In addition, at least half of the pathways towards the biosynthesis of essential amino acids, its proposed symbiotic function, are completely or partially lost. CONCLUSION: We propose that this strain of C. ruddii can be viewed as a further step towards the degeneration of the former primary endosymbiont and its transformation in a subcellular new entity between living cells and organelles. Although the transition of genes from C. ruddii to the host nucleus has been proposed, the amount of genes that should have been transferred to the germinal line of the insect would be so big that it would be more plausible to consider the implication of the mitochondrial machinery encoded in the insect nucleus. Furthermore, since most genes for the biosynthesis of essential amino acids have also been lost, it is likely that the host depends on another yet unidentified symbiont to complement its deficient diet. BioMed Central 2007-10-01 /pmc/articles/PMC2175510/ /pubmed/17908294 http://dx.doi.org/10.1186/1471-2148-7-181 Text en Copyright © 2007 Tamames 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
Tamames, Javier
Gil, Rosario
Latorre, Amparo
Peretó, Juli
Silva, Francisco J
Moya, Andrés
The frontier between cell and organelle: genome analysis of Candidatus Carsonella ruddii
title The frontier between cell and organelle: genome analysis of Candidatus Carsonella ruddii
title_full The frontier between cell and organelle: genome analysis of Candidatus Carsonella ruddii
title_fullStr The frontier between cell and organelle: genome analysis of Candidatus Carsonella ruddii
title_full_unstemmed The frontier between cell and organelle: genome analysis of Candidatus Carsonella ruddii
title_short The frontier between cell and organelle: genome analysis of Candidatus Carsonella ruddii
title_sort frontier between cell and organelle: genome analysis of candidatus carsonella ruddii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175510/
https://www.ncbi.nlm.nih.gov/pubmed/17908294
http://dx.doi.org/10.1186/1471-2148-7-181
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