Summary
We have investigated the mechanism of division inhibition in E. coli following UV-irradiation or nalidixic acid treatment. After UV, two separate mechanisms, both dependent upon recA, appear to block division. One mechanism is dependent upon sfiA and sfiB, is inhibited by low levels (4 μg/ml) of rifamycin and is expressed in tif mutants at 42°C. The second mechanism is dependent on sfiA, B, is resistant to rifamycin and does not occur in cells lacking DNA replication forks. We suggest that this second mechanism is the result of the failure to terminate DNA replication in inhibited cells.
Nalidixic acid inhibition of cell division also appears to involve both mechanisms but as found previously replication forks are also necessary to induce the sfi pathway.
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References
Brent R, Ptashne M (1981) The lexA gene product represses its own promoter. Proc Natl Acad Sci USA 78:4204–4208
Castallazzi M, George J, Buttin G (1972) Prophage induction and cell division in E. coli I. Further characterisation of a thermosensitive mutation tif1 whose expression mimics the effect of UV-irradiation. Mol Gen Genet 119:139–152
Cooper S, Helmstetter CE (1981) Chromosome replication and the division cycle of Escherichia coli. J Mol Biol 31:519–540
Darby V (1981) Inhibition of cell division in Escherichia coli K12 by UV-irradiation. Ph.D. Thesis University of Leicester
Darby V, Holland IB (1979) A kinetic analysis of cell division, and induction and instability of recA protein in U.V. irradiated lon + and lon − strains of Escherichia coli K12. Mol Gen Genet 176:121–128
Fogliano M, Schendel PF (1981) Evidence for the inducibility of the uvrB operon. Nature 289:196–198
George J, Castellazzi M, Buttin G (1975) Prophage induction and cell division of E. coli. III Mutations sfiA and sfiB restore division in tif and lon strains and permit the expression of mutator properties of tif. Mol Gen Genet 140:309–332
Gudas LJ, Pardee AB (1975) A model for the regulation of Escherichia coli DNA repair function. Proc Natl Acad Sci USA 72:2330–2334
Helmstetter CE, Pierucci O (1968) Cell division during inhibition of deoxyribonucleic acid synthesis in Escherichia coli. J Bacteriol 95:1627–1633
Helmstetter CE, Pierucci O, Weinberger M, Holmes M, Tang MS (1979) In: The bacteria vol VII. Mechanisms of adaptation. Sokatch JR, Ornston LN (eds) Academic Press Inc, New York, pp 517–579
Huisman O, D'Ari R, George J (1980a) Dissociation of tsl-tif-induced filamentation and recA protein synthesis in Escherichia K12. J Bacteriol 142:819–828
Huisman O, D'Ari R, George J (1980b) Further characterisation of sfiA and sfiB mutations in Escherichia coli. J Bacteriol 144:185–191
Huisman O, D'Ari R (1981) An inducible DNA replication-cell division coupling mechanism in E. coli. Nature 290:797–799
Inouye M (1971) Pleiotropic effect of the recA gene of Escherichia coli: uncoupling of cell division from deoxyribonucleic acid replication. J Bacteriol 106:539–542
Kenyon CJ, Walker GC (1981) Expression of the E. coli uvrA gene is inducible. Nature 289:808–810
Lark KG, Lark C (1978) RecA dependent DNA replication in the absence of protein synthesis: characteristics of a dominant lethal replication mutation dnaT and requirement for recA + function. Cold Spring Harbor Symp Quant Biol 43:537–549
Little JW, Edmiston SH, Pacelli LZ, Mount, DW (1980) Cleavage of the Escherichia coli lexA protein by the recA protease. Proc Natl Acad Sci USA 77:3225–3229
Little, JW, Mount DW, Yanisch-Perron C (1981) Purified lexA protein is a repressor of the recA and lexA genes. Proc Natl Acad Sci USA 78:4199–4203
McEntee K (1978) Studies of the recA and lexA genes of E. coli K12. In: Hanawalt PC, Friedberg EC, Fox CF (ed) DNA repair mechanisms. ICN-UCLA Symposia on Molecular and Cellular Biology. Academic Press, Inc, New York, pp 349–359
Pacelli LZ, Edmiston, SH, Mount DW (1979) Isolation and characterisation of amber mutations in the lexA gene of Escherichia coli K12. J Bacteriol 137:568–573
Powell EO (1956) Growth rate and generation time of bacteria with special reference to continuous culture. J Gen Microbiol 15:492–511
Radman M (1975) In: Hanawalt PC, Setlow RB (eds) Molecular mechanisms for repair of DNA. Basic Life Sci 5:355–369
Satta G, Pardee AB (1978) Inhibtion of Escherichia coli division by protein X. J Bacteriol 133:1492–1500
Witkin EM (1967) The radiation sensitivity of Escherichia coli B: a hypothesis relating filament formation and prophage induction. Proc Natl Acad Sci USA 57:1275–1279
Witkin EM (1976) Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli. Bacteriol Rev 40:869–907
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Burton, P., Barry Holland, I. Two pathways of division inhibition in UV-irradiated E. coli . Mol Gen Genet 190, 128–132 (1983). https://doi.org/10.1007/BF00330334
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DOI: https://doi.org/10.1007/BF00330334