Moolenaar G F, van Sluis C A, Backendorf C, van de Putte P
Nucleic Acids Res. 1987 May 26;15(10):4273-89. doi: 10.1093/nar/15.10.4273.
The UvrA, UvrB and UvrC proteins of E. coli are subunits of a DNA repair enzyme, the ABC exonuclease. In this paper we study the uvrC regulatory region. The uvrC structural gene is preceded by an open reading frame encoding a 24 kD protein. A uvrC promoter has been mapped within this gene. The transcription start of a second promoter located 5' of the 24 kD gene is mapped in vivo. We show that transcription from both promoters on the chromosome is not inducible by UV damage. The possible translation start codons of the UvrC and of the 24 kD protein are determined. Sequences encoding the N-terminal part of the UvrC protein overlap with sequences encoding the C-terminal part of the 24 kD protein. To examine a possible function of the 24 kD gene in repair, a 24 kD insertion mutant was created in the chromosome. The mutant however only slightly affects the UV sensitivity of the cell. Transcription of P3 alone provides sufficient UvrC protein for the normal repair of UV lesions.
大肠杆菌的UvrA、UvrB和UvrC蛋白是一种DNA修复酶即ABC核酸外切酶的亚基。在本文中,我们研究了uvrC调控区。uvrC结构基因之前有一个编码24kD蛋白的开放阅读框。已在该基因内定位了一个uvrC启动子。在体内定位了位于24kD基因5'端的第二个启动子的转录起始位点。我们表明,染色体上两个启动子的转录都不能被紫外线损伤诱导。确定了UvrC和24kD蛋白可能的翻译起始密码子。编码UvrC蛋白N端部分的序列与编码24kD蛋白C端部分的序列重叠。为了研究24kD基因在修复中的可能功能,在染色体上创建了一个24kD插入突变体。然而,该突变体仅对细胞的紫外线敏感性有轻微影响。单独的P3转录为紫外线损伤的正常修复提供了足够的UvrC蛋白。