Iwaki T, Kawamura A, Ishino Y, Kohno K, Kano Y, Goshima N, Yara M, Furusawa M, Doi H, Imamoto F
Department of Molecular Genetics, Kyoto Pharmaceutical University, Japan.
Mol Gen Genet. 1996 Jul 26;251(6):657-64. doi: 10.1007/BF02174114.
The mutation frequencies attributable to -1 frameshift or one-base substitution in the structural genes coding for resistance to chloramphenicol (Cm) and tetracycline (Tc) were followed over several cycles of DNA replication, and found to differ several-fold, depending on the orientation of the gene on the plasmid with respect to the direction of (unidirectional ColE1-type) replication. The mutation frequency was higher when the reporter gene was present in the plasmid in the same orientation as the direction of the origin, i.e., when the transcription template is the lagging daughter strand, than when the gene was inserted in the opposite orientation. This significant difference in reversion frequencies of genes with different polarities was demonstrated only for a brief period of cell growth (several cycles of replication) after induction of the dnaQ49 mutator, but was not observed when an increased number of replication cycles, was permitted, most probably due to fixation of the mutation into both strands. The mutated intermediate DNA which possesses a misaligned basepair in the Cm gene was demonstrated to be replicated into two progeny DNA molecules; one is the chloramphenicol-resistant (CmR) DNA synthesized from the template strand having the mutation and the other is the CmS DNA from the template strand without mutation. Our results suggest that replication-dependent mutagenesis may occur preferentially in the lagging strand.
在编码对氯霉素(Cm)和四环素(Tc)耐药性的结构基因中,归因于 -1 移码或单碱基替换的突变频率在 DNA 复制的几个周期中进行跟踪,发现其相差几倍,这取决于质粒上基因相对于(单向 ColE1 型)复制方向的方向。当报告基因在质粒中的方向与原点方向相同时,即转录模板是滞后子链时,突变频率高于基因以相反方向插入时。仅在诱导 dnaQ49 诱变剂后的细胞生长短暂时期(几个复制周期)内,才证明具有不同极性的基因回复频率存在这种显著差异,但当允许增加复制周期数时未观察到这种差异,这很可能是由于突变固定到两条链中。已证明在 Cm 基因中具有错配碱基对的突变中间 DNA 被复制成两个子代 DNA 分子;一个是由具有突变的模板链合成的氯霉素抗性(CmR)DNA,另一个是来自无突变模板链的 CmS DNA。我们的结果表明,依赖复制的诱变可能优先发生在滞后链中。