Abstract
The gene orders in the genomes of nine alpha-proteobacteria were compared using quantitative indices S (the relative number of common pairs of adjacent genes) and L (the mean difference between intergenic distances). A sample of 200 homologous genes, occurring in all 11 strains, was studied. In all of the genomes examined, 20 conserved, “uninterrupted” regions, including in total 63 out of 200 genes, were found. The rate of evolutionary change in the gene order widely varied in different evolutionary lineages. The highest rate (40 to 60 genome rearrangements per 100 Myr) was characteristic of the intercellular parasite Wolbachia (Rickettsiales). Computer simulation has showed that the S to L ratio observed in the sample testified that the probability of large genome rearrangements was somewhat lower than that of small ones.
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REFERENCES
Zakharov, I.A. and Valeev, A.K., Quantitative Analysis of Mammalian Genome Evolution by Comparing Genetic Maps, Dokl. Akad. Nauk SSSR, 1988, vol. 301, pp. 1213–1218.
Zakharov, I.A., Nikiforov, V.S., and Stepanyuk, E.V., Homology and Evolution of Gene Orders: A Simple Method for Testing a Hypothesis on the Pattern of This Evolution, Rus. J. Genet., 1996, vol. 32, no.1, pp. 112–116.
Zakharov, I.A., Measurements of Similarity of Synteny Groups and an Analysis of Genome Rearrangemetns in the Evolution of Mammals, Bioinformatics and Genome Research: Proc. 3d Int. Conf., Lim, H.A. and Cantor, C.R., Eds., Singapore: World Sci., 1995, pp. 107–113.
Zakharov, I.A., Nikiforov, V.S., and Stepanyuk, E.V., Homology and Evolution of Gene Orders: A Combinatorial Measure of Similarity of Synteny Groups and Modeling of the Evolutionary Process, Genetika (Moscow), 1992, vol. 28, no.1, pp. 77–81.
Zakharov, I.A., Nikiforov, V.S., and Stepanyuk, E.V., Homology and Evolution of Gene Orders: Simulation and Reconstruction of the Evolutionary Process, Rus. J. Genet., 1997, vol. 33, no.1, pp. 24–30.
Zakharov, I.A., Nikiforov, V.S., and Stepanyuk, E.V., Measurement of Similarity between Orders of Homologous Genes, Genetika (Moscow), 1991, vol. 27, no.2, pp. 367–369.
Sankoff, D., Leduc, G., Antoine, N., et al., Gene Order Comparisons for Phylogenetic Inference: Evolution of Mitochondrial Genome, Proc. Natl. Acad. Sci. USA, 1992, vol. 89, pp. 6575–6579.
Blanchette, M., Kunisawa, T., and Sankoff, D., Gene Order Breakpoint Evidence in Animal Mitochondrial Phylogeny, J. Mol. Evol., 1999, vol. 49, pp. 193–203.
Ehrlich, J., Sankoff, D., and Nadeau, J.H., Synteny Conservation and Chromosome Rearrangements during Mammalian Evolution, Genetics, 1997, vol. 147, no.1, pp. 289–296.
Suyama, M. and Bork, P., Evolution of Prokaryotic Gene Order: Genome Rearrangements in Closely Related Species, Trends Genet., 2001, vol. 21, pp. 10–13.
Belda, E., Moya, A., and Silva, F.J., Genome Rearrangement Distances and Gene Order Phylogeny in γ-Proteobacteria, Mol. Biol. Evol., 2005, vol. 22, pp. 1456–1467.
Wu, M., Sun, L.V., Vamathevan, J., et al., Phylogenomics of the Reproductive Parasite Wolbachia pipientis WMel: A Streamlined Genome Overrun by Mobile Genetic Elements, PLoS Biol., 2004, vol. 2, no.3, pp. 327–341.
Bandi, C., Anderson, T.J.C., Genchi, C., and Blaxter, M.L., Phylogeny of Wolbachia-Like Bacteria in Filarial Nematodes, Proc. R. Soc. London, B, 1998, vol. 265, pp. 2407–2413.
Zakharov, I.A. and Markov, A.V., Intracellular Parasite Wolbachia and the Origin of Eukaryotes, Usp. Sovrem. Biol., 2005, vol. 125, pp. 323–336.
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Translated from Genetika, Vol. 41, No. 12, 2005, pp. 1624–1633.
Original Russian Text Copyright © 2005 by Zakharov, Markov.
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Zakharov, I.A., Markov, A.V. Gene Orders in Genomes of Alpha-Proteobacteria: Similarity and Evolution. Russ J Genet 41, 1343–1351 (2005). https://doi.org/10.1007/s11177-006-0005-8
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DOI: https://doi.org/10.1007/s11177-006-0005-8