DNA repair in Mycobacterium tuberculosis.: What have we learnt from the genome sequence?

被引:142
作者
Mizrahi, V
Andersen, SJ
机构
[1] S African Inst Med Res, Mol Biol Unit, ZA-2000 Johannesburg, South Africa
[2] Univ Witwatersrand, Dept Haematol, Johannesburg, South Africa
关键词
D O I
10.1046/j.1365-2958.1998.01038.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页码:1331 / 1339
页数:9
相关论文
共 73 条
[1]  
Altschul SF, 1996, METHOD ENZYMOL, V266, P460
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]   The PROSITE database, its status in 1997 [J].
Bairoch, A ;
Bucher, P ;
Hofmann, K .
NUCLEIC ACIDS RESEARCH, 1997, 25 (01) :217-221
[4]   Effect of mutY and mutM/fpg-1 mutations on starvation-associated mutation in Escherichia coli: Implications for the role of 7,8-dihydro-8-oxoguanine [J].
Bridges, BA ;
Sekiguchi, M ;
Tajiri, T .
MOLECULAR & GENERAL GENETICS, 1996, 251 (03) :352-357
[5]   Microbial genetics - Hypermutation under stress [J].
Bridges, BA .
NATURE, 1997, 387 (6633) :557-558
[6]   Mutation in Escherichia coli under starvation conditions: A new pathway leading to small deletions in strains defective in mismatch correction [J].
Bridges, BA ;
Timms, AR .
EMBO JOURNAL, 1997, 16 (11) :3349-3356
[7]  
Cole S T, 1995, Eur Respir J Suppl, V20, p701s
[8]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[9]  
Colston M. Joseph, 1994, P217
[10]  
COLSTON MJ, 1998, KEYST S TB MOL MECH