Lundberg L G, Thoresson H O, Karlström O H, Nyman P O
EMBO J. 1983;2(6):967-71. doi: 10.1002/j.1460-2075.1983.tb01529.x.
The nucleotide sequence of the dUTPase structural gene, dut, of Escherichia coli has been determined. The DNA sequence predicts a polypeptide chain of 150 amino acid residues (mol. wt. 16 006) corresponding in size and composition to the purified dUTPase subunit. In a tentative promoter region preceding the dut gene, the -35 and -10 regions are separated by a SacI (SstI) site. Cloning of the dut gene utilization this SacI site was previously shown to reduce dut expression dramatically. The nucleotide sequence also contains a 210-codon open reading frame 106 bp downstream of dut and co-directional with dut. Previous protein synthesis experiments using dut plasmids allocated the gene of a polypeptide of mol. wt. 23 500 to this DNA region. The open reading frame thus may correspond to a protein of unknown function co-transcribed with the dut gene.
已确定大肠杆菌dUTPase结构基因dut的核苷酸序列。DNA序列预测有一条由150个氨基酸残基组成的多肽链(分子量为16006),其大小和组成与纯化的dUTPase亚基相对应。在dut基因之前的一个暂定启动子区域,-35区和-10区被一个SacI(SstI)位点隔开。先前已表明利用这个SacI位点克隆dut基因会显著降低dut的表达。核苷酸序列还包含一个位于dut下游106 bp处且与dut同向的210密码子开放阅读框。先前使用dut质粒进行的蛋白质合成实验将分子量为23500的一种多肽的基因定位到了这个DNA区域。因此,该开放阅读框可能对应于一个与dut基因共转录的功能未知的蛋白质。