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. 2009 Nov 23:4:46.
doi: 10.1186/1745-6150-4-46.

Evolution by leaps: gene duplication in bacteria

Affiliations

Affiliation

  • 1 Josephine Bay Paul Center, Marine Biological Laboratory, Woods Hole, MA 02543, USA. mserres@mbl.edu

Evolution by leaps: gene duplication in bacteria

Margrethe H Serres et al. Biol Direct. .
. 2009 Nov 23:4:46.
doi: 10.1186/1745-6150-4-46.

Affiliation

  • 1 Josephine Bay Paul Center, Marine Biological Laboratory, Woods Hole, MA 02543, USA. mserres@mbl.edu

Abstract

Background: Sequence related families of genes and proteins are common in bacterial genomes. In Escherichia coli they constitute over half of the genome. The presence of families and superfamilies of proteins suggest a history of gene duplication and divergence during evolution. Genome encoded protein families, their size and functional composition, reflect metabolic potentials of the organisms they are found in. Comparing protein families of different organisms give insight into functional differences and similarities.

Results: Equivalent enzyme families with metabolic functions were selected from the genomes of four experimentally characterized bacteria belonging to separate genera. Both similarities and differences were detected in the protein family memberships, with more similarities being detected among the more closely related organisms. Protein family memberships reflected known metabolic characteristics of the organisms. Differences in divergence of functionally characterized enzyme family members accounted for characteristics of taxa known to differ in those biochemical properties and capabilities. While some members of the gene families will have been acquired by lateral exchange and other former family members will have been lost over time, duplication and divergence of genes and functions appear to have been a significant contributor to the functional diversity of today's microbes.

Conclusions: Protein families seem likely to have arisen during evolution by gene duplication and divergence where the gene copies that have been retained are the variants that have led to distinct bacterial physiologies and taxa. Thus divergence of the duplicate enzymes has been a major process in the generation of different kinds of bacteria.

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Figures

Figure 1

Figure 1

Alignment of the E. coli

Figure 1

Alignment of the E. coli ribose transport protein RbsB and the ribose repressor…
Figure 1
Alignment of the E. coli ribose transport protein RbsB and the ribose repressor RbsR. The protein sequences were aligned with ClustalW 2.0.11. Identical residues are highlighted in dark grey while conserved and semi-conserved residues are highlighted in light grey.
Figure 2

Figure 2

Alignment of E. coli SDR…

Figure 2

Alignment of E. coli SDR family members . The enzymes of the family…
Figure 2
Alignment of E. coli SDR family members. The enzymes of the family members are listed in Table 1. Four conserved regions of the proteins are shown. The protein sequences were aligned with ClustalW 2.0.11. Identical residues are highlighted in dark grey while conserved and semi-conserved residues are highlighted in light grey.
Figure 3

Figure 3

Alignment of E. coli crotonase…

Figure 3

Alignment of E. coli crotonase family members . Protein family membership was determined…
Figure 3
Alignment of E. coli crotonase family members. Protein family membership was determined as proteins having sequence similarity of 200 Pam units or less over at least 50% of their length. Members of the E. coli crotonase family are listed in Table 3. The protein sequences were aligned with ClustalW 2.0.11. Identical residues are highlighted in dark grey while conserved and semi-conserved residues are highlighted in light grey. Residues forming the FadB oxanion hole used to stabilize reaction intermediates are shown in bold-face. The FadB reaction center is outlined.

References

    1. Koonin EV. Darwinian evolution in the light of genomics. Nucleic Acids Res. 2009;37:1011–1034. doi: 10.1093/nar/gkp089. - DOI - PMC - PubMed
    1. Kimura M. The Neutral Theory of Molecular Evolution. Cambridge: Cambridge University Press; 1983.
    1. Ohno S. Evolution by Gene Duplication. New York: Springer-Verlag; 1970. pp. 1–160.
    1. Yanai I, Camacho CJ, DeLisi C. Predictions of gene family distributions in microbial genomes: evolution by gene duplication and modification. Phys Rev Lett. 2000;85:2641–2644. doi: 10.1103/PhysRevLett.85.2641. - DOI - PubMed
    1. Raes J, Peer Y Van de. Gene duplication, the evolution of novel gene functions, and detecting functional divergence of duplicates in silico. Appl Bioinformatics. 2003;2:91–101. - PubMed

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