McKenzie G J, Harris R S, Lee P L, Rosenberg S M
Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.
Proc Natl Acad Sci U S A. 2000 Jun 6;97(12):6646-51. doi: 10.1073/pnas.120161797.
Upon starvation some Escherichia coli cells undergo a transient, genome-wide hypermutation (called adaptive mutation) that is recombination-dependent and appears to be a response to a stressful environment. Adaptive mutation may reflect an inducible mechanism that generates genetic variability in times of stress. Previously, however, the regulatory components and signal transduction pathways controlling adaptive mutation were unknown. Here we show that adaptive mutation is regulated by the SOS response, a complex, graded response to DNA damage that includes induction of gene products blocking cell division and promoting mutation, recombination, and DNA repair. We find that SOS-induced levels of proteins other than RecA are needed for adaptive mutation. We report a requirement of RecF for efficient adaptive mutation and provide evidence that the role of RecF in mutation is to allow SOS induction. We also report the discovery of an SOS-controlled inhibitor of adaptive mutation, PsiB. These results indicate that adaptive mutation is a tightly regulated response, controlled both positively and negatively by the SOS system.
在饥饿状态下,一些大肠杆菌细胞会经历短暂的全基因组超突变(称为适应性突变),这种突变依赖于重组,似乎是对压力环境的一种反应。适应性突变可能反映了一种在压力时期产生遗传变异性的诱导机制。然而,以前控制适应性突变的调控成分和信号转导途径尚不清楚。在这里,我们表明适应性突变受SOS反应调控,SOS反应是对DNA损伤的一种复杂的分级反应,包括诱导阻止细胞分裂以及促进突变、重组和DNA修复的基因产物。我们发现适应性突变需要SOS诱导的除RecA之外的蛋白质水平。我们报告了RecF对有效适应性突变的需求,并提供证据表明RecF在突变中的作用是允许SOS诱导。我们还报告了发现一种受SOS控制的适应性突变抑制剂PsiB。这些结果表明适应性突变是一种受到严格调控的反应,由SOS系统进行正向和负向控制。