Seidman M M, Bredberg A, Seetharam S, Kraemer K H
Proc Natl Acad Sci U S A. 1987 Jul;84(14):4944-8. doi: 10.1073/pnas.84.14.4944.
Mutagenesis was studied at the DNA-sequence level in human fibroblast and lymphoid cells by use of a shuttle vector plasmid, pZ189, containing a suppressor tRNA marker gene. In a series of experiments, 62 plasmids were recovered that had two to six base substitutions in the 160-base-pair marker gene. Approximately 20-30% of the mutant plasmids that were recovered after passing ultraviolet-treated pZ189 through a repair-proficient human fibroblast line contained these multiple mutations. In contrast, passage of ultraviolet-treated pZ189 through an excision-repair-deficient (xeroderma pigmentosum) line yielded only 2% multiple base substitution mutants. Introducing a single-strand nick in otherwise unmodified pZ189 adjacent to the marker, followed by passage through the xeroderma pigmentosum cells, resulted in about 66% multiple base substitution mutants. The multiple mutations were found in a 160-base-pair region containing the marker gene but were rarely found in an adjacent 170-base-pair region. Passing ultraviolet-treated or nicked pZ189 through a repair-proficient human B-cell line also yielded multiple base substitution mutations in 20-33% of the mutant plasmids. An explanation for these multiple mutations is that they were generated by an error-prone polymerase while filling gaps. These mutations share many of the properties displayed by mutations in the immunoglobulin hypervariable regions.
利用含有抑制性tRNA标记基因的穿梭载体质粒pZ189,在人类成纤维细胞和淋巴细胞的DNA序列水平上研究了诱变作用。在一系列实验中,回收了62个质粒,这些质粒在160个碱基对的标记基因中有两到六个碱基替换。经过紫外线处理的pZ189通过具有修复能力的人类成纤维细胞系后回收的突变体质粒中,约20%-30%含有这些多重突变。相比之下,经过紫外线处理的pZ189通过切除修复缺陷型(着色性干皮病)细胞系后,仅产生2%的多重碱基替换突变体。在标记附近未修饰的pZ189中引入一个单链切口,然后通过着色性干皮病细胞,产生了约66%的多重碱基替换突变体。多重突变出现在包含标记基因的160个碱基对区域,但在相邻的170个碱基对区域中很少发现。经过紫外线处理或有切口的pZ189通过具有修复能力的人类B细胞系后,20%-33%的突变体质粒也产生了多重碱基替换突变。对这些多重突变的一种解释是,它们是在填补缺口时由易出错的聚合酶产生的。这些突变具有许多免疫球蛋白高变区突变所表现出的特性。