Cargando…

Comparative mitochondrial genomics of snakes: extraordinary substitution rate dynamics and functionality of the duplicate control region

BACKGROUND: The mitochondrial genomes of snakes are characterized by an overall evolutionary rate that appears to be one of the most accelerated among vertebrates. They also possess other unusual features, including short tRNAs and other genes, and a duplicated control region that has been stably ma...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiang, Zhi J, Castoe, Todd A, Austin, Christopher C, Burbrink, Frank T, Herron, Matthew D, McGuire, Jimmy A, Parkinson, Christopher L, Pollock, David D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950710/
https://www.ncbi.nlm.nih.gov/pubmed/17655768
http://dx.doi.org/10.1186/1471-2148-7-123
_version_ 1782134572418334720
author Jiang, Zhi J
Castoe, Todd A
Austin, Christopher C
Burbrink, Frank T
Herron, Matthew D
McGuire, Jimmy A
Parkinson, Christopher L
Pollock, David D
author_facet Jiang, Zhi J
Castoe, Todd A
Austin, Christopher C
Burbrink, Frank T
Herron, Matthew D
McGuire, Jimmy A
Parkinson, Christopher L
Pollock, David D
author_sort Jiang, Zhi J
collection PubMed
description BACKGROUND: The mitochondrial genomes of snakes are characterized by an overall evolutionary rate that appears to be one of the most accelerated among vertebrates. They also possess other unusual features, including short tRNAs and other genes, and a duplicated control region that has been stably maintained since it originated more than 70 million years ago. Here, we provide a detailed analysis of evolutionary dynamics in snake mitochondrial genomes to better understand the basis of these extreme characteristics, and to explore the relationship between mitochondrial genome molecular evolution, genome architecture, and molecular function. We sequenced complete mitochondrial genomes from Slowinski's corn snake (Pantherophis slowinskii) and two cottonmouths (Agkistrodon piscivorus) to complement previously existing mitochondrial genomes, and to provide an improved comparative view of how genome architecture affects molecular evolution at contrasting levels of divergence. RESULTS: We present a Bayesian genetic approach that suggests that the duplicated control region can function as an additional origin of heavy strand replication. The two control regions also appear to have different intra-specific versus inter-specific evolutionary dynamics that may be associated with complex modes of concerted evolution. We find that different genomic regions have experienced substantial accelerated evolution along early branches in snakes, with different genes having experienced dramatic accelerations along specific branches. Some of these accelerations appear to coincide with, or subsequent to, the shortening of various mitochondrial genes and the duplication of the control region and flanking tRNAs. CONCLUSION: Fluctuations in the strength and pattern of selection during snake evolution have had widely varying gene-specific effects on substitution rates, and these rate accelerations may have been functionally related to unusual changes in genomic architecture. The among-lineage and among-gene variation in rate dynamics observed in snakes is the most extreme thus far observed in animal genomes, and provides an important study system for further evaluating the biochemical and physiological basis of evolutionary pressures in vertebrate mitochondria.
format Text
id pubmed-1950710
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-19507102007-08-23 Comparative mitochondrial genomics of snakes: extraordinary substitution rate dynamics and functionality of the duplicate control region Jiang, Zhi J Castoe, Todd A Austin, Christopher C Burbrink, Frank T Herron, Matthew D McGuire, Jimmy A Parkinson, Christopher L Pollock, David D BMC Evol Biol Research Article BACKGROUND: The mitochondrial genomes of snakes are characterized by an overall evolutionary rate that appears to be one of the most accelerated among vertebrates. They also possess other unusual features, including short tRNAs and other genes, and a duplicated control region that has been stably maintained since it originated more than 70 million years ago. Here, we provide a detailed analysis of evolutionary dynamics in snake mitochondrial genomes to better understand the basis of these extreme characteristics, and to explore the relationship between mitochondrial genome molecular evolution, genome architecture, and molecular function. We sequenced complete mitochondrial genomes from Slowinski's corn snake (Pantherophis slowinskii) and two cottonmouths (Agkistrodon piscivorus) to complement previously existing mitochondrial genomes, and to provide an improved comparative view of how genome architecture affects molecular evolution at contrasting levels of divergence. RESULTS: We present a Bayesian genetic approach that suggests that the duplicated control region can function as an additional origin of heavy strand replication. The two control regions also appear to have different intra-specific versus inter-specific evolutionary dynamics that may be associated with complex modes of concerted evolution. We find that different genomic regions have experienced substantial accelerated evolution along early branches in snakes, with different genes having experienced dramatic accelerations along specific branches. Some of these accelerations appear to coincide with, or subsequent to, the shortening of various mitochondrial genes and the duplication of the control region and flanking tRNAs. CONCLUSION: Fluctuations in the strength and pattern of selection during snake evolution have had widely varying gene-specific effects on substitution rates, and these rate accelerations may have been functionally related to unusual changes in genomic architecture. The among-lineage and among-gene variation in rate dynamics observed in snakes is the most extreme thus far observed in animal genomes, and provides an important study system for further evaluating the biochemical and physiological basis of evolutionary pressures in vertebrate mitochondria. BioMed Central 2007-07-26 /pmc/articles/PMC1950710/ /pubmed/17655768 http://dx.doi.org/10.1186/1471-2148-7-123 Text en Copyright © 2007 Jiang 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
Jiang, Zhi J
Castoe, Todd A
Austin, Christopher C
Burbrink, Frank T
Herron, Matthew D
McGuire, Jimmy A
Parkinson, Christopher L
Pollock, David D
Comparative mitochondrial genomics of snakes: extraordinary substitution rate dynamics and functionality of the duplicate control region
title Comparative mitochondrial genomics of snakes: extraordinary substitution rate dynamics and functionality of the duplicate control region
title_full Comparative mitochondrial genomics of snakes: extraordinary substitution rate dynamics and functionality of the duplicate control region
title_fullStr Comparative mitochondrial genomics of snakes: extraordinary substitution rate dynamics and functionality of the duplicate control region
title_full_unstemmed Comparative mitochondrial genomics of snakes: extraordinary substitution rate dynamics and functionality of the duplicate control region
title_short Comparative mitochondrial genomics of snakes: extraordinary substitution rate dynamics and functionality of the duplicate control region
title_sort comparative mitochondrial genomics of snakes: extraordinary substitution rate dynamics and functionality of the duplicate control region
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950710/
https://www.ncbi.nlm.nih.gov/pubmed/17655768
http://dx.doi.org/10.1186/1471-2148-7-123
work_keys_str_mv AT jiangzhij comparativemitochondrialgenomicsofsnakesextraordinarysubstitutionratedynamicsandfunctionalityoftheduplicatecontrolregion
AT castoetodda comparativemitochondrialgenomicsofsnakesextraordinarysubstitutionratedynamicsandfunctionalityoftheduplicatecontrolregion
AT austinchristopherc comparativemitochondrialgenomicsofsnakesextraordinarysubstitutionratedynamicsandfunctionalityoftheduplicatecontrolregion
AT burbrinkfrankt comparativemitochondrialgenomicsofsnakesextraordinarysubstitutionratedynamicsandfunctionalityoftheduplicatecontrolregion
AT herronmatthewd comparativemitochondrialgenomicsofsnakesextraordinarysubstitutionratedynamicsandfunctionalityoftheduplicatecontrolregion
AT mcguirejimmya comparativemitochondrialgenomicsofsnakesextraordinarysubstitutionratedynamicsandfunctionalityoftheduplicatecontrolregion
AT parkinsonchristopherl comparativemitochondrialgenomicsofsnakesextraordinarysubstitutionratedynamicsandfunctionalityoftheduplicatecontrolregion
AT pollockdavidd comparativemitochondrialgenomicsofsnakesextraordinarysubstitutionratedynamicsandfunctionalityoftheduplicatecontrolregion