TableEdit

Davis, EO, Dullaghan, EM and Rand, L (2002) Definition of the mycobacterial SOS box and use to identify LexA-regulated genes in Mycobacterium tuberculosis. J. Bacteriol. 184:3287-95

The bases of the mycobacterial SOS box important for LexA binding were determined by replacing each base with every other and examining the effect on the induction of a reporter gene following DNA damage. This analysis revealed that the SOS box was longer than originally thought by 2 bp in each half of the palindromic site. A search of the Mycobacterium tuberculosis genome sequence with the new consensus, TCGAAC(N)(4)GTTCGA, identified 4 sites which were perfect matches and 12 sites with a single mismatch which were predicted to bind LexA. Genes which could potentially be regulated by these SOS boxes were ascertained from their positions relative to the sites. Examination of expression data for these genes following DNA damage identified 12 new genes which are most likely regulated by LexA as well as the known M. tuberculosis DNA damage-inducible genes recA, lexA, and ruvC. Of these 12 genes, only 2 have a predicted function: dnaE2, a component of DNA polymerase III, and linB, which is similar to 1,3,4,6-tetrachloro-1,4-cylcohexadiene hydrolase. Curiously, of the remaining 10 genes predicted to be LexA regulated, 7 are members of the M. tuberculosis 13E12 repeat family, which has some of the characteristics of mobile elements.

PubMed PMC135081

Bacterial Proteins/genetics; Bacterial Proteins/metabolism; Base Sequence; DNA Damage; Gene Expression Profiling; Gene Expression Regulation, Bacterial; Molecular Sequence Data; Mycobacterium tuberculosis/genetics; Mycobacterium tuberculosis/metabolism; Oligonucleotide Array Sequence Analysis; Rec A Recombinases/genetics; SOS Response (Genetics)/genetics; SOS Response (Genetics)/physiology; Serine Endopeptidases/genetics; Serine Endopeptidases/metabolism