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Nucleic Acids Research 2005 33(8):2603-2614; doi:10.1093/nar/gki551
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Published online 10 May 2005

© The Author 2005. Published by Oxford University Press. All rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions{at}oupjournals.org


Article

An SOS-regulated operon involved in damage-inducible mutagenesis in Caulobacter crescentus

Rodrigo S. Galhardo, Raquel P. Rocha, Marilis V. Marques and Carlos F. M. Menck*

Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo São Paulo, SP 05508-900, Brazil

*To whom correspondence should be addressed at Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, Avenue Professor Lineu Prestes, 1374, São Paulo, SP 05508-900, Brazil. Tel: +55 11 3091 7499; Fax: +55 11 3091 7354; Email: cfmmenck{at}usp.br

Received February 25, 2005. Revised April 15, 2005. Accepted April 15, 2005.

DNA polymerases of the Y-family, such as Escherichia coli UmuC and DinB, are specialized enzymes induced by the SOS response, which bypass lesions allowing the continuation of DNA replication. umuDC orthologs are absent in Caulobacter crescentus and other bacteria, raising the question about the existence of SOS mutagenesis in these organisms. Here, we report that the C.crescentus dinB ortholog is not involved in damage-induced mutagenesis. However, an operon composed of two hypothetical genes and dnaE2, encoding a second copy of the catalytic subunit of Pol III, is damage inducible in a recA-dependent manner, and is responsible for most ultraviolet (UV) and mitomycin C-induced mutations in C.crescentus. The results demonstrate that the three genes are required for the error-prone processing of DNA lesions. The two hypothetical genes were named imuA and imuB, after inducible mutagenesis. ImuB is similar to proteins of the Y-family of polymerases, and possibly cooperates with DnaE2 in lesion bypass. The mutations arising as a consequence of the activity of the imuAB dnaE2 operon are rather unusual for UV irradiation, including G:C to C:G transversions.


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