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Molecular Evolution of the Hyperthermophilic Archaea of the Pyrococcus Genus: Analysis of Adaptation to Different Environmental Conditions

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2010 Jan 1
PMID 20042074
Citations 13
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Abstract

Background: Prokaryotic microorganisms are able to survive and proliferate in severe environmental conditions. The increasing number of complete sequences of prokaryotic genomes has provided the basis for studying the molecular mechanisms of their adaptation at the genomic level. We apply here a computer-based approach to compare the genomes and proteomes from P. furiosus, P. horikoshii, and P. abyssi to identify features of their molecular evolution related to adaptation strategy to diverse environmental conditions.

Results: Phylogenetic analysis of rRNA genes from 26 Pyrococcus strains suggested that the divergence of P. furiosus, P. horikoshii and P. abyssi might have occurred from ancestral deep-sea organisms. It was demonstrated that the function of genes that have been subject to positive Darwinian selection is closely related to abiotic and biotic conditions to which archaea managed to become adapted. Divergence of the P. furiosus archaea might have been due to loss of some genes involved in cell motility or signal transduction, and/or to evolution under positive selection of the genes for translation machinery. In the course of P. horikoshii divergence, positive selection was found to operate mainly on the transcription machinery; divergence of P. abyssi was related with positive selection for the genes mainly involved in inorganic ion transport. Analysis of radical amino acid replacement rate in evolving P. furiosus, P. horikoshii and P. abyssi showed that the fixation rate was higher for radical substitutions relative to the volume of amino acid side-chain.

Conclusions: The current results give due credit to the important role of hydrostatic pressure as a cause of variability in the P. furiosus, P. horikoshii and P. abyssi genomes evolving in different habitats. Nevertheless, adaptation to pressure does not appear to be the sole factor ensuring adaptation to environment. For example, at the stage of the divergence of P. horikoshii and P. abyssi, an essential evolutionary role may be assigned to changes in the trophic chain, namely, acquisition of a consumer status at a high (P. horikoshii) or low level (P. abyssi).

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References
1.
Burggraf S, HUBER H, Stetter K . Reclassification of the crenarchael orders and families in accordance with 16S rRNA sequence data. Int J Syst Bacteriol. 1997; 47(3):657-60. DOI: 10.1099/00207713-47-3-657. View

2.
Niven G, Miles C, Mackey B . The effects of hydrostatic pressure on ribosome conformation in Escherichia coli: and in vivo study using differential scanning calorimetry. Microbiology (Reading). 1999; 145 ( Pt 2):419-425. DOI: 10.1099/13500872-145-2-419. View

3.
Adachi J, Waddell P, Martin W, Hasegawa M . Plastid genome phylogeny and a model of amino acid substitution for proteins encoded by chloroplast DNA. J Mol Evol. 2000; 50(4):348-58. DOI: 10.1007/s002399910038. View

4.
Kanoksilapatham W, Gonzalez J, Maeder D, DiRuggiero J, Robb F . A proposal to rename the hyperthermophile Pyrococcus woesei as Pyrococcus furiosus subsp. woesei. Archaea. 2005; 1(4):277-83. PMC: 2685572. DOI: 10.1155/2004/513563. View

5.
Maeder D, Weiss R, Dunn D, Cherry J, Gonzalez J, DiRuggiero J . Divergence of the hyperthermophilic archaea Pyrococcus furiosus and P. horikoshii inferred from complete genomic sequences. Genetics. 1999; 152(4):1299-305. PMC: 1460691. DOI: 10.1093/genetics/152.4.1299. View