DNA repair in Mycobacterium tuberculosis. What have we learnt from the genome sequence?
- 2 September 1998
- journal article
- research article
- Published by Wiley in Molecular Microbiology
- Vol. 29 (6) , 1331-1339
- https://doi.org/10.1046/j.1365-2958.1998.01038.x
Abstract
The genome sequence of Mycobacterium tuberculosis was analysed by searching for homologues of genes known to be involved in the reversal or repair of DNA damage in Escherichia coli and related organisms. Genes necessary to perform nucleotide excision repair (NER), base excision repair (BER), recombination, and SOS repair and mutagenesis were identified. In particular, all of the genes known to be directly involved in the repair of oxidative and alkylative damage are present in M. tuberculosis. In contrast, we failed to identify homologues of genes involved in mismatch repair. This finding has potentially significant implications with respect to genome stability, strain variability at repeat loci and the emergence of chromosomally encoded drug resistance mutations.This publication has 70 references indexed in Scilit:
- Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequenceNature, 1998
- A eukaryotic SPB/ERCC3-like helicase in Mycobacterium leprae?Trends in Biochemical Sciences, 1997
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- Characterization of Mycobacterium tuberculosis LexA: recognition of a Cheo (Bacillus-type SOS) boxMicrobiology, 1997
- Functional Characterization of the Precursor and Spliced Forms of RecA Protein of Mycobacterium tuberculosisBiochemistry, 1996
- Is Mycobacterium tuberculosis 15,000 Years Old?The Journal of Infectious Diseases, 1994
- Strain variation in the katG region of Mycobacterium tuberculosisMolecular Microbiology, 1994
- Involvement of RecF pathway recombination genes in postreplication repair in UV-irradiated Escherichia coli cellsMutation Research/DNA Repair, 1994
- Protein splicing in the maturation of M. tuberculosis RecA protein: A mechanism for tolerating a novel class of intervening sequenceCell, 1992
- BACTERIAL MUTATOR GENES AND THE CONTROL OF SPONTANEOUS MUTATIONAnnual Review of Genetics, 1976