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Journal of Bacteriology, August 2009, p. 5076-5084, Vol. 191, No. 16
0021-9193/09/$08.00+0 doi:10.1128/JB.00254-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.
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Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024
Received 25 February 2009/ Accepted 8 June 2009
RecBCD and AddAB are bacterial enzymes that share similar helicase and nuclease activities and initiate repair of DNA double-strand breaks by homologous recombination. Examination of the phylogenetic distribution of AddAB and RecBCD revealed that one or the other complex is present in most sequenced bacteria. In addition, horizontal gene transfer (HGT) events involving addAB and recBCD appear to be common, with the genes encoding one complex frequently replacing those encoding the other. HGT may also explain the unexpected identification of archaeal addAB genes. More than 85% of addAB and recBCD genes are clustered on the genome, suggesting operon structures. A few organisms, including the Mycobacteria, encode multiple copies of these complexes of either the same or mixed classes. The possibility that the enzymatic activities of the AddAB and RecBCD enzymes promote their horizontal transfer is discussed, and the distribution of AddAB/RecBCD is compared to that of the RecU/RuvC resolvases. Finally, it appears that two sequence motifs, the Walker A box involved in ATP binding and an iron-sulfur-cysteine cluster, are present only in subsets of AddB proteins, suggesting the existence of mechanistically distinct classes of AddB.
Published ahead of print on 19 June 2009.
Supplemental material for this article may be found at http://jb.asm.org/.
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