Chromosome Segregation and Cell Division Defects in Recombination Mutants Exposed to Different DNA-Damaging Treatments.

Homologous recombination repairs potentially lethal DNA lesions such as double-strand DNA breaks (DSBs) and single-strand DNA gaps (SSGs). In , DSB repair is initiated by the RecBCD enzyme that resects double-strand DNA ends and loads RecA recombinase to the emerging single-strand (ss) DNA tails. SSG repair is mediated by the RecFOR protein complex that loads RecA onto the ssDNA segment of gaped duplex. In both repair pathways, RecA catalyses reactions of homologous DNA pairing and strand exchange, while RuvABC complex and RecG helicase process recombination intermediates. In this work, we have characterised cytological changes in various recombination mutants of after three different DNA-damaging treatments: (i) expression of I-I endonuclease, (ii) γ-irradiation, and (iii) UV-irradiation. All three treatments caused severe chromosome segregation defects and DNA-less cell formation in the , and mutants. After I-I expression and γ-irradiation, this phenotype was efficiently suppressed by the mutation, indicating that cytological defects result mostly from incomplete DSB repair. In UV-irradiated cells, the mutation abolished cytological defects of mutants and also partially suppressed the cytological defects of mutants. However, neither nor mutation alone could suppress the cytological defects of UV-irradiated mutants. The suppression was achieved only by simultaneous inactivation of the and genes. Cell survival and microscopic analysis suggest that chromosome segregation defects in UV-irradiated mutants largely result from defective processing of stalled replication forks. The results of this study show that chromosome morphology is a valuable marker in genetic analyses of recombinational repair in .