Berger H, Brammar W J, Yanofsky C
J Bacteriol. 1968 Nov;96(5):1672-9. doi: 10.1128/jb.96.5.1672-1679.1968.
Frameshift mutant trpA21 was isolated after ultraviolet treatment and frameshift mutant trpA540 after ICR191-A (an acridine derivative) treatment of wild-type Escherichia coli K-12. The A proteins of spontaneous and ICR191-A-induced partial revertants of these mutants contained altered amino acid sequences one residue shorter than the comparable sequence in the A protein of wild-type bacteria. The data support the conclusion that ICR191-A causes frameshift mutations. The findings further indicate that both base additions and deletions are elicited by ICR191-A treatment and that mutagenesis by this compound sometimes affects more than one base pair. ICR191-A also weakly reverts some missense mutants. Analyses of the relevant peptides of the purified A protein show single amino acid replacements compatible with single base-pair changes. In addition, we found that some spontaneously revertible ICR191-A- and ultraviolet light-induced frameshift mutants are not further stimulated to revert by exposure to ultraviolet light.
移码突变体trpA21是在对野生型大肠杆菌K - 12进行紫外线处理后分离得到的,而移码突变体trpA540是在对野生型大肠杆菌K - 12进行ICR191 - A(一种吖啶衍生物)处理后得到的。这些突变体的自发及ICR191 - A诱导的部分回复突变体的A蛋白含有改变的氨基酸序列,比野生型细菌A蛋白中的可比序列少一个残基。这些数据支持ICR191 - A导致移码突变的结论。研究结果进一步表明,ICR191 - A处理会引发碱基的添加和缺失,并且该化合物的诱变有时会影响不止一个碱基对。ICR191 - A也能使一些错义突变体发生弱回复突变。对纯化的A蛋白相关肽段的分析显示,单个氨基酸替换与单个碱基对变化相符。此外,我们发现一些可自发回复的ICR191 - A和紫外线诱导的移码突变体,在暴露于紫外线后不会进一步被刺激发生回复突变。