Ogasawara N, Moriya S, Mazza G, Yoshikawa H
Gene. 1986;45(2):227-31. doi: 10.1016/0378-1119(86)90259-3.
A dnaG mutation of Bacillus subtilis, dnaG5, was found to be linked closely to recF. We have reported previously that two putative dna genes, 'dnaA' and 'dnaN', highly homologous to Escherichia coli's dnaA and dnaN, respectively, were located adjacent to recF [Ogasawara et al., EMBO J., 4 (1985) 3345-3350]. Transformation by various fragments cloned from the 'dnaA'-recF region of the wild-type cell revealed that a 532-bp AluI fragment containing 5'-portion of the 'dnaN' gene could transform the dnaG5 mutation. The nucleotide (nt) sequence of the same fragment cloned from the mutant cell shows a single nt change in the ORF of 'dnaN' which in turn causes a single amino acid alteration from Gly to Arg. The 'dnaN' gene is now proven to be a dna gene, mutations in which result in instant arrest of chromosomal replication.
枯草芽孢杆菌的一个dnaG突变体dnaG5被发现与recF紧密连锁。我们之前报道过,两个分别与大肠杆菌的dnaA和dnaN高度同源的假定dna基因“dnaA”和“dnaN”位于recF附近[小笠原等人,《欧洲分子生物学组织杂志》,4(1985)3345 - 3350]。从野生型细胞的“dnaA”-recF区域克隆的各种片段进行转化实验表明,一个包含“dnaN”基因5'端部分的532 bp AluI片段能够转化dnaG5突变体。从突变体细胞克隆的相同片段的核苷酸(nt)序列显示,“dnaN”的开放阅读框(ORF)中有一个单核苷酸变化,进而导致一个氨基酸从甘氨酸变为精氨酸。现在已证明“dnaN”基因是一个dna基因,其突变会导致染色体复制立即停止。