Control of the LexA regulon by pH: evidence for a reversible inactivation of the LexA repressor during the growth cycle of Escherichia coli
- 1 May 1994
- journal article
- Published by Wiley in Molecular Microbiology
- Vol. 12 (4) , 621-629
- https://doi.org/10.1111/j.1365-2958.1994.tb01049.x
Abstract
The LexA repressor controls the expression of several genes, including lexA, recA, and sfiA, which are induced when exponentially growing bacteria are exposed to DNA-damaging agents. Induction of this so-called SOS response takes place while LexA is cleaved in a reaction that requires the RecA protein and damaged DNA. We have shown that large fluctuations in the cellular concentration of the LexA repressor and in the rate of transcription of the sfiA gene also occur spontaneously during bacterial growth in complex medium such as LB. The possibility that changes in external or internal pH may explain these fluctuations has been explored. A consistent pattern was established whereby conditions leading to either increased or decreased pH were associated with altered expression of the lexA and sfiA genes. These data can be explained by a model in which the LexA repressor exists in either of two forms in equilibrium: a form favoured at homeostatic internal pH, which has a low affinity for the operators of LexA-controlled genes; and a form accumulated in response to a transient decrease in internal pH, which has a high affinity for operators.Keywords
This publication has 43 references indexed in Scilit:
- Phosphate starvation and low temperature as well as ultraviolet irradiation transcriptionally induce the Escherichia coli LexA‐controlled gene sfiAMolecular Microbiology, 1993
- Isolation and characterization of LexA mutant repressers with enhanced DNA binding affinityJournal of Molecular Biology, 1992
- Dimerization of a Specific DNA-Binding Protein on the DNAScience, 1992
- DNA binding properties of the LexA repressorBiochimie, 1991
- Nature of the SOS-inducing signal in Escherichia coliJournal of Molecular Biology, 1990
- The LexA repressor and its isolated amino-terminal domain interact cooperatively with poly[d(A-T)], a contiguous pseudo-operator, but not with random DNA: a circular dichroism studyBiochemistry, 1990
- Effects of overproduction of single-stranded DNA-binding protein on RecA protein-dependent processes in Escherichia coliJournal of Molecular Biology, 1987
- In vitro study of the interaction of the LexA represser and the UvrC protein with a uvrC regulatory regionFEBS Letters, 1986
- Transcription of the sulA gene and repression by LexAJournal of Molecular Biology, 1983
- Induction of prophage λ does not require full induction of RecA protein synthesisBiochimie, 1980