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用DNA损伤剂处理可增加大肠杆菌K-12中polA'-'lacZ基因融合体的表达。

Treatment with DNA-damaging agents increases expression of polA'-'lacZ gene fusions in Escherichia coli K-12.

作者信息

Wandt G, Kubis S, Quiñones A

机构信息

Deutsche Forschungsgemeinschaft, Bonn, FRG.

出版信息

Mol Gen Genet. 1997 Mar 18;254(1):98-103. doi: 10.1007/s004380050396.

Abstract

The polA gene of Escherichia coli encodes the DNA polymerase I that is involved in DNA replication and repair. In contrast to the extensive body of data on the structure and function of polymerase I, there is little information available concerning the mechanisms that govern polA expression. Here, we studied the expression of the polA gene using translational fusions to lacZ. We found that treatment with the DNA-damaging agents 4-nitroquinoline-N-oxide (4-NQO), UV light mitomycin C (MC) and methyl methanesulfonate (MMS) leads to enhanced expression of polA'-'lacZ fusions. The increase in expression of polA reflects stimulation of transcription from a single promoter, as determined by S1 nuclease analyses. This was not observed in mutants that are blocked in induction of the SOS regulon. However, mutants with defective excision repair were more susceptible to polA stimulation. These results support the hypothesis that increased polA expression may be important for the ability to repair bulky DNA adducts that interfere with replication.

摘要

大肠杆菌的polA基因编码参与DNA复制和修复的DNA聚合酶I。与关于聚合酶I结构和功能的大量数据相比,关于调控polA表达的机制的信息却很少。在这里,我们使用与lacZ的翻译融合来研究polA基因的表达。我们发现,用DNA损伤剂4-硝基喹啉-N-氧化物(4-NQO)、紫外线、丝裂霉素C(MC)和甲基磺酸甲酯(MMS)处理会导致polA'-'lacZ融合体的表达增强。如通过S1核酸酶分析所确定的,polA表达的增加反映了来自单个启动子的转录受到刺激。在SOS调节子诱导受阻的突变体中未观察到这种情况。然而,切除修复有缺陷的突变体对polA刺激更敏感。这些结果支持这样的假设,即polA表达增加对于修复干扰复制的大分子DNA加合物的能力可能很重要。

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