Benson F E, Illing G T, Sharples G J, Lloyd R G
Department of Genetics, Queen's Medical Centre, University of Nottingham, UK.
Nucleic Acids Res. 1988 Feb 25;16(4):1541-9. doi: 10.1093/nar/16.4.1541.
The nucleotide sequence of a 2505 bp region of the Escherichia coli chromosome containing the LexA regulated ruv gene has been determined. A sequence of 1631 bp encoding two non-overlapping open reading frames that constitute a single operon and which specify polypeptides with predicted molecular weights of 22172 daltons and 37177 daltons respectively, was identified as the most probable sequence for ruv. Each of the two open reading frames, designated ruvA and ruvB, is preceded by a reasonable Shine-Dalgarno sequence. Two 16 bp sequences (SOS boxes) that match the consensus sequence for binding LexA protein are located 5' to ruvA in a region that provides a possible single promoter for expression of both ruvA and ruvB, with the second SOS box overlapping the putative -35 region. A possible transcriptional terminator is located 137 bp downstream of ruvB. The amino acid sequence predicted for RuvB contains a region that matches a highly conserved sequence found in several DNA repair and recombination proteins that bind ATP.
已确定大肠杆菌染色体中包含受LexA调控的ruv基因的2505 bp区域的核苷酸序列。一段1631 bp的序列编码两个不重叠的开放阅读框,它们构成一个单一操纵子,并分别指定预测分子量为22172道尔顿和37177道尔顿的多肽,该序列被确定为ruv最可能的序列。两个开放阅读框分别命名为ruvA和ruvB,每个阅读框之前都有一个合理的Shine-Dalgarno序列。两个与LexA蛋白结合的共有序列匹配的16 bp序列(SOS框)位于ruvA的5'端,该区域可能为ruvA和ruvB的表达提供单一启动子,第二个SOS框与推定的-35区域重叠。一个可能的转录终止子位于ruvB下游137 bp处。预测的RuvB氨基酸序列包含一个与几种结合ATP的DNA修复和重组蛋白中发现的高度保守序列相匹配的区域。