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Genetics and Molecular Biology |
Division of Mycobacterial Research, National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK1
Author for correspondence: K. G. Papavinasasundaram. Tel: +44 20 8959 3666. Fax: +44 20 8913 8528. e-mail: kpapavi{at}nimr.mrc.ac.uk
In mycobacteria, as in most bacterial species, the expression of RecA is induced by DNA damage. However, the authors show here that the kinetics of recA induction in Mycobacterium smegmatis and in Mycobacterium tuberculosis are quite different: whilst maximum expression in M. smegmatis occurred 36 h after addition of a DNA-damaging agent, incubation for 1836 h was required to reach peak levels in M. tuberculosis. This is despite the fact that the M. tuberculosis promoter can be activated more rapidly when transferred to M. smegmatis. In addition, it is demonstrated that in both species the DNA is sufficiently damaged to give maximum induction within the first hour of incubation with mitomycin C. The difference in the induction kinetics of recA between the two species was mirrored by a difference in the levels of DNA-binding-competent LexA following DNA damage. A decrease in the ability of LexA to bind to the SOS box was readily detected by 2 h in M. smegmatis, whilst a decrease was not apparent until 1824 h in M. tuberculosis and then only a very small decrease was observed.
Keywords: LexA, SOS induction, mycobacteria
a Present address: Trescowthick Research Laboratories, Peter MacCallum Cancer Institute, Locked Bag 1, ABeckett Street, Melbourne VIC 8006, Australia.
b Present address: London School of Hygiene and Tropical Medicine, Keppel Street, London WC1E 7HT, UK.
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