Villaverde A, Gibert I, Barbé J
Department of Genetics and Microbiology, Autonomous University of Barcelona, Spain.
Mutat Res. 1988 May;199(1):123-30. doi: 10.1016/0027-5107(88)90237-0.
The kinetics of the recA, sfiA and umuDC genes transcription were studied during a double SOS-inducing treatment in Escherichia coli cells using several strains carrying lacZ gene fusions. A transient inhibition in recA, but not in sfiA or umuDC promoted beta-galactosidase synthesis was detected after successive UV-irradiations. Results obtained with a recA--lacZ fusion introduced in several DNA-repair mutants demonstrated that neither a lower LexA inactivation nor a decrease in the production of the inducing signal are the events through which the successive UV-irradiation promoted the arrest of recA transcription. On the contrary, a specific UV-dose-dependent delay appears to be the reason for the inhibition of the recA gene transcription in cells irradiated twice.
利用几种携带lacZ基因融合体的菌株,研究了大肠杆菌细胞在双重SOS诱导处理过程中recA、sfiA和umuDC基因转录的动力学。连续紫外线照射后,检测到recA基因转录有短暂抑制,但sfiA或umuDC基因转录促进的β-半乳糖苷酶合成未受抑制。在几个DNA修复突变体中引入recA-lacZ融合体所获得的结果表明,连续紫外线照射促进recA转录停止,既不是通过较低的LexA失活,也不是通过诱导信号产生的减少。相反,特定的紫外线剂量依赖性延迟似乎是两次照射细胞中recA基因转录受到抑制的原因。