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The planetary biology of cytochrome P450 aromatases

BACKGROUND: Joining a model for the molecular evolution of a protein family to the paleontological and geological records (geobiology), and then to the chemical structures of substrates, products, and protein folds, is emerging as a broad strategy for generating hypotheses concerning function in a p...

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Autores principales: Gaucher, Eric A, Graddy, Logan G, Li, Tang, Simmen, Rosalia CM, Simmen, Frank A, Schreiber, David R, Liberles, David A, Janis, Christine M, Benner, Steven A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC515309/
https://www.ncbi.nlm.nih.gov/pubmed/15315709
http://dx.doi.org/10.1186/1741-7007-2-19
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author Gaucher, Eric A
Graddy, Logan G
Li, Tang
Simmen, Rosalia CM
Simmen, Frank A
Schreiber, David R
Liberles, David A
Janis, Christine M
Benner, Steven A
author_facet Gaucher, Eric A
Graddy, Logan G
Li, Tang
Simmen, Rosalia CM
Simmen, Frank A
Schreiber, David R
Liberles, David A
Janis, Christine M
Benner, Steven A
author_sort Gaucher, Eric A
collection PubMed
description BACKGROUND: Joining a model for the molecular evolution of a protein family to the paleontological and geological records (geobiology), and then to the chemical structures of substrates, products, and protein folds, is emerging as a broad strategy for generating hypotheses concerning function in a post-genomic world. This strategy expands systems biology to a planetary context, necessary for a notion of fitness to underlie (as it must) any discussion of function within a biomolecular system. RESULTS: Here, we report an example of such an expansion, where tools from planetary biology were used to analyze three genes from the pig Sus scrofa that encode cytochrome P450 aromatases–enzymes that convert androgens into estrogens. The evolutionary history of the vertebrate aromatase gene family was reconstructed. Transition redundant exchange silent substitution metrics were used to interpolate dates for the divergence of family members, the paleontological record was consulted to identify changes in physiology that correlated in time with the change in molecular behavior, and new aromatase sequences from peccary were obtained. Metrics that detect changing function in proteins were then applied, including K(A)/K(S )values and those that exploit structural biology. These identified specific amino acid replacements that were associated with changing substrate and product specificity during the time of presumed adaptive change. The combined analysis suggests that aromatase paralogs arose in pigs as a result of selection for Suoidea with larger litters than their ancestors, and permitted the Suoidea to survive the global climatic trauma that began in the Eocene. CONCLUSIONS: This combination of bioinformatics analysis, molecular evolution, paleontology, cladistics, global climatology, structural biology, and organic chemistry serves as a paradigm in planetary biology. As the geological, paleontological, and genomic records improve, this approach should become widely useful to make systems biology statements about high-level function for biomolecular systems.
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spelling pubmed-5153092004-09-03 The planetary biology of cytochrome P450 aromatases Gaucher, Eric A Graddy, Logan G Li, Tang Simmen, Rosalia CM Simmen, Frank A Schreiber, David R Liberles, David A Janis, Christine M Benner, Steven A BMC Biol Research Article BACKGROUND: Joining a model for the molecular evolution of a protein family to the paleontological and geological records (geobiology), and then to the chemical structures of substrates, products, and protein folds, is emerging as a broad strategy for generating hypotheses concerning function in a post-genomic world. This strategy expands systems biology to a planetary context, necessary for a notion of fitness to underlie (as it must) any discussion of function within a biomolecular system. RESULTS: Here, we report an example of such an expansion, where tools from planetary biology were used to analyze three genes from the pig Sus scrofa that encode cytochrome P450 aromatases–enzymes that convert androgens into estrogens. The evolutionary history of the vertebrate aromatase gene family was reconstructed. Transition redundant exchange silent substitution metrics were used to interpolate dates for the divergence of family members, the paleontological record was consulted to identify changes in physiology that correlated in time with the change in molecular behavior, and new aromatase sequences from peccary were obtained. Metrics that detect changing function in proteins were then applied, including K(A)/K(S )values and those that exploit structural biology. These identified specific amino acid replacements that were associated with changing substrate and product specificity during the time of presumed adaptive change. The combined analysis suggests that aromatase paralogs arose in pigs as a result of selection for Suoidea with larger litters than their ancestors, and permitted the Suoidea to survive the global climatic trauma that began in the Eocene. CONCLUSIONS: This combination of bioinformatics analysis, molecular evolution, paleontology, cladistics, global climatology, structural biology, and organic chemistry serves as a paradigm in planetary biology. As the geological, paleontological, and genomic records improve, this approach should become widely useful to make systems biology statements about high-level function for biomolecular systems. BioMed Central 2004-08-17 /pmc/articles/PMC515309/ /pubmed/15315709 http://dx.doi.org/10.1186/1741-7007-2-19 Text en Copyright © 2004 Gaucher et al; licensee BioMed Central Ltd.
spellingShingle Research Article
Gaucher, Eric A
Graddy, Logan G
Li, Tang
Simmen, Rosalia CM
Simmen, Frank A
Schreiber, David R
Liberles, David A
Janis, Christine M
Benner, Steven A
The planetary biology of cytochrome P450 aromatases
title The planetary biology of cytochrome P450 aromatases
title_full The planetary biology of cytochrome P450 aromatases
title_fullStr The planetary biology of cytochrome P450 aromatases
title_full_unstemmed The planetary biology of cytochrome P450 aromatases
title_short The planetary biology of cytochrome P450 aromatases
title_sort planetary biology of cytochrome p450 aromatases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC515309/
https://www.ncbi.nlm.nih.gov/pubmed/15315709
http://dx.doi.org/10.1186/1741-7007-2-19
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