Involvement of recA and recF in the induced precise excision of Tn10 in Escherichia coli

被引:11
作者
Chan, A [1 ]
Nagel, R [1 ]
机构
[1] CONSEJO NACL INVEST CIENT & TECN,CEFYBO,RA-1414 BUENOS AIRES,DF,ARGENTINA
关键词
Tn10 precise excision; uvrD mutant; recF mutant; SOS gene; recombination repair; Escherichia coli;
D O I
10.1016/S0027-5107(97)00157-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
It has been shown that the increased frequency of precise excision of Tn10 observed after UV or mitomycin C (MMC) treatment or with uvrD- mutants is recA-dependent. Previous work has also shown that expression of SOS genes is required for W-or MMC-induced Tn10 precise excision. In order to determine if the increased excision of Tn10 in uvrD- mutants requires only expression of recA, or expression of other SOS genes, or both, we studied the precise excision of Tn10 in lexA3 (Ind-, SOS non-inducible) and lexA3 recAo98 (operator constitutive recA) mutants. The results of these experiments indicate that the induced excision of Tn10 in the uvrD- null mutant depends on the expression of recA rather than on any of the other genes repressed by LexA. The effect of a null recF mutation on the excision of Tn10 in a uvrD- mutant was also investigated and found to abolish the increased frequencies of this process. Similarly, the recF mutation was found to decrease markedly the increased precise excision of Tn10 induced by MMC in a uvrD+ isogenic strain. These observations indicate that recA and recF are involved in the increased frequencies of Tn10 excision exhibited by uvrD- mutants or after MMC treatment. It remains to be determined whether these two genes participate in these two induction processes in the same biochemical pathways. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:111 / 115
页数:5
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