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On the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the Common Pathway genes

BACKGROUND: The lysine, threonine, and methionine biosynthetic pathways share the three initial enzymatic steps, which are referred to as the Common Pathway (CP). In Escherichia coli three different aspartokinases (AKI, AKII, AKIII, the products of thrA, metL and lysC, respectively) can perform the...

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Autores principales: Fondi, Marco, Brilli, Matteo, Fani, Renato
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1885841/
https://www.ncbi.nlm.nih.gov/pubmed/17430556
http://dx.doi.org/10.1186/1471-2105-8-S1-S12
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author Fondi, Marco
Brilli, Matteo
Fani, Renato
author_facet Fondi, Marco
Brilli, Matteo
Fani, Renato
author_sort Fondi, Marco
collection PubMed
description BACKGROUND: The lysine, threonine, and methionine biosynthetic pathways share the three initial enzymatic steps, which are referred to as the Common Pathway (CP). In Escherichia coli three different aspartokinases (AKI, AKII, AKIII, the products of thrA, metL and lysC, respectively) can perform the first step of the CP. Moreover, two of them (AKI and AKII) are bifunctional, carrying also homoserine dehydrogenasic activity (hom product). The second step of the CP is catalyzed by a single aspartate semialdehyde dehydrogenase (ASDH, the product of asd). Thus, in the CP of E. coli while a single copy of ASDH performs the same reaction for three different metabolic routes, three different AKs perfom a unique step. Why and how such a situation did emerge and maintain? How is it correlated to the different regulatory mechanisms acting on these genes? The aim of this work was to trace the evolutionary pathway leading to the extant scenario in proteobacteria. RESULTS: The analysis of the structure, organization, phylogeny, and distribution of ask and hom genes revealed that the presence of multiple copies of these genes and their fusion events are restricted to the γ-subdivision of proteobacteria. This allowed us to depict a model to explain the evolution of ask and hom according to which the fused genes are the outcome of a cascade of gene duplication and fusion events that can be traced in the ancestor of γ-proteobacteria. Moreover, the appearance of fused genes paralleled the assembly of operons of different sizes, suggesting a strong correlation between the structure and organization of these genes. A statistic analysis of microarray data retrieved from experiments carried out on E. coli and Pseudomonas aeruginosa was also performed. CONCLUSION: The integration of data concerning gene structure, organization, phylogeny, distribution, and microarray experiments allowed us to depict a model for the evolution of ask and hom genes in proteobacteria and to suggest a biological significance for the extant scenario.
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spelling pubmed-18858412007-06-05 On the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the Common Pathway genes Fondi, Marco Brilli, Matteo Fani, Renato BMC Bioinformatics Research BACKGROUND: The lysine, threonine, and methionine biosynthetic pathways share the three initial enzymatic steps, which are referred to as the Common Pathway (CP). In Escherichia coli three different aspartokinases (AKI, AKII, AKIII, the products of thrA, metL and lysC, respectively) can perform the first step of the CP. Moreover, two of them (AKI and AKII) are bifunctional, carrying also homoserine dehydrogenasic activity (hom product). The second step of the CP is catalyzed by a single aspartate semialdehyde dehydrogenase (ASDH, the product of asd). Thus, in the CP of E. coli while a single copy of ASDH performs the same reaction for three different metabolic routes, three different AKs perfom a unique step. Why and how such a situation did emerge and maintain? How is it correlated to the different regulatory mechanisms acting on these genes? The aim of this work was to trace the evolutionary pathway leading to the extant scenario in proteobacteria. RESULTS: The analysis of the structure, organization, phylogeny, and distribution of ask and hom genes revealed that the presence of multiple copies of these genes and their fusion events are restricted to the γ-subdivision of proteobacteria. This allowed us to depict a model to explain the evolution of ask and hom according to which the fused genes are the outcome of a cascade of gene duplication and fusion events that can be traced in the ancestor of γ-proteobacteria. Moreover, the appearance of fused genes paralleled the assembly of operons of different sizes, suggesting a strong correlation between the structure and organization of these genes. A statistic analysis of microarray data retrieved from experiments carried out on E. coli and Pseudomonas aeruginosa was also performed. CONCLUSION: The integration of data concerning gene structure, organization, phylogeny, distribution, and microarray experiments allowed us to depict a model for the evolution of ask and hom genes in proteobacteria and to suggest a biological significance for the extant scenario. BioMed Central 2007-03-08 /pmc/articles/PMC1885841/ /pubmed/17430556 http://dx.doi.org/10.1186/1471-2105-8-S1-S12 Text en Copyright © 2007 Fondi 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
Fondi, Marco
Brilli, Matteo
Fani, Renato
On the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the Common Pathway genes
title On the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the Common Pathway genes
title_full On the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the Common Pathway genes
title_fullStr On the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the Common Pathway genes
title_full_unstemmed On the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the Common Pathway genes
title_short On the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the Common Pathway genes
title_sort on the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the common pathway genes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1885841/
https://www.ncbi.nlm.nih.gov/pubmed/17430556
http://dx.doi.org/10.1186/1471-2105-8-S1-S12
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