Different patterns of evolution for duplicated DNA repair genes in bacteria of the Xanthomonadales group


Autoria(s): Martins-Pinheiro, Marinalva ; Galhardo, Rodrigo S; Lage, Claudia ; Lima-Bessa, Keronninn M; Aires, Karina A; Menck, Carlos FM
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

26/08/2013

26/08/2013

01/08/2004

Resumo

Abstract Background DNA repair genes encode proteins that protect organisms against genetic damage generated by environmental agents and by-products of cell metabolism. The importance of these genes in life maintenance is supported by their high conservation, and the presence of duplications of such genes may be easily traced, especially in prokaryotic genomes. Results The genome sequences of two Xanthomonas species were used as the basis for phylogenetic analyses of genes related to DNA repair that were found duplicated. Although 16S rRNA phylogenetic analyses confirm their classification at the basis of the gamma proteobacteria subdivision, differences were found in the origin of the various genes investigated. Except for lexA, detected as a recent duplication, most of the genes in more than one copy are represented by two highly divergent orthologs. Basically, one of such duplications is frequently positioned close to other gamma proteobacteria, but the second is often positioned close to unrelated bacteria. These orthologs may have occurred from old duplication events, followed by extensive gene loss, or were originated from lateral gene transfer (LGT), as is the case of the uvrD homolog. Conclusions Duplications of DNA repair related genes may result in redundancy and also improve the organisms' responses to environmental challenges. Most of such duplications, in Xanthomonas, seem to have arisen from old events and possibly enlarge both functional and evolutionary genome potentiality.

The authors thank Dr. Sérgio Russo Matioli (University of São Paulo, Brazil) for helpful discussion. Financial support was obtained from FAPESP (São Paulo, Brazil) and CNPq (Brasília, Brazil).

The authors thank Dr. Sérgio Russo Matioli (University of São Paulo, Brazil) for helpful discussion. Financial support was obtained from FAPESP (São Paulo, Brazil) and CNPq (Brasília, Brazil).

Identificador

BMC Evolutionary Biology. 2004 Aug 27;4(1):29

1471-2148

http://www.producao.usp.br/handle/BDPI/32749

10.1186/1471-2148-4-29

http://www.biomedcentral.com/1471-2148/4/29

Idioma(s)

eng

Relação

BMC Evolutionary Biology

Direitos

openAccess

Martins-Pinheiro et al; licensee BioMed Central Ltd. - 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.

Tipo

article

original article