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The mismatch repair system ( mutS , mutL and uvrD genes) in Pseudomonas aeruginosa : molecular characterization of naturally occurring mutants
Author(s) -
Oliver Antonio,
Baquero Fernando,
Blázquez Jesús
Publication year - 2002
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1046/j.1365-2958.2002.02855.x
Subject(s) - dna mismatch repair , biology , mutant , genetics , gene , dna repair , escherichia coli , nucleotide excision repair , mutation , pseudomonas aeruginosa , complementation , microbiology and biotechnology , bacteria
Summary We have recently described the presence of a high proportion of Pseudomonas aeruginosa isolates (20%) with an increased mutation frequency (mutators) in the lungs of cystic fibrosis (CF) patients. In four out of 11 independent P. aeruginosa strains, the high mutation frequency was found to be complemented with the wild‐type mutS gene from P. aeruginosa PAO1. Here, we report the cloning and sequencing of two additional P. aeruginosa mismatch repair genes and the characterization, by complementation of deficient strains, of these two putative P. aeruginosa mismatch repair genes ( mutL and uvrD ). We also describe the alterations in the mutS , mutL and uvrD genes responsible for the mutator phenotype of hypermutable P. aeruginosa strains isolated from CF patients. Seven out of the 11 mutator strains were found to be defective in the MMR system (four mutS , two mutL and one uvrD ). In four cases (three mutS and one mutL ), the genes contained frameshift mutations. The fourth mutS strain showed a 3.3 kb insertion after the 10th nucleotide of the mutS gene, and a 54 nucleotide deletion between two eight nucleotide direct repeats. This deletion, involving domain II of MutS, was found to be the main one responsible for mutS inactivation. The second mutL strain presented a K310M mutation, equivalent to K307 in Escherichia coli MutL, a residue known to be essential for its ATPase activity. Finally, the uvrD strain had three amino acid substitutions within the conserved ATP binding site of the deduced UvrD polypeptide, showing defective mismatch repair activity. Interestingly, cells carrying this mutant allele exhibited a fully active UvrABC‐mediated excision repair. The results shown here indicate that the putative P. aeruginosa mutS , mutL and uvrD genes are mutator genes and that their alteration results in a mutator phenotype.