Mao J R, Inouye S, Inouye M
Department of Biochemistry, Robert Wood Johnson Medical School, Piscataway, NJ, USA.
FEMS Microbiol Lett. 1996 Oct 15;144(1):109-15. doi: 10.1111/j.1574-6968.1996.tb08516.x.
A minor population of wild Escherichia coli strains contain retroelements called retrons, which produce a peculiar satellite DNA, multicopy single-stranded DNA (msDNA). It has been reported that mismatched base pairs in the secondary structure formed in msDNA are mutagenic in E. coli[Maas et al.(1994) Mol.Microbiol. 14,437-441; Maas et al. (1996) Mol. Microbiol, 19, 505-509]. We reexamined this proposal by converting mismatched base pairs to matched base pairs using a single msDNA species, msDNA-Ec86, or by deleting mismatched regions using msDNA-Ec73. We also examined the effect of reverse transcriptases (RT) without msDNA production on mutagenesis. All the constructs are under the lpp/lac promoter-operator control so that their mutagenic effects can be tested in the absence and the presence of a lac inducer. It was found that when the production of msDNA-Ec86 or Ec73 was induced, reversion frequencies from Lac- to Lac+ significantly increased in the case of a Lac- mutation caused by a frame-shift mutation, but much less by a substitution mutation. The removal of mismatched base pairs eliminated the high mutation frequencies, and the inducible expression of RT alone was not mutagenic. These results are consistent with the hypothesis of Maas and his associates that mismatched base pairs in msDNA sequester a cellular mismatch repair system, resulting in the increase of frame-shift mutations.
一小部分野生大肠杆菌菌株含有称为反转录子的反转元件,这些元件会产生一种特殊的卫星DNA,即多拷贝单链DNA(msDNA)。据报道,msDNA中形成的二级结构中的错配碱基对在大肠杆菌中具有致突变性[马斯等人(1994年),《分子微生物学》,第14卷,第437 - 441页;马斯等人(1996年),《分子微生物学》,第19卷,第505 - 509页]。我们通过使用单一的msDNA种类msDNA - Ec86将错配碱基对转换为匹配碱基对,或使用msDNA - Ec73删除错配区域,重新审视了这一观点。我们还研究了不产生msDNA的逆转录酶(RT)对诱变的影响。所有构建体都受lpp/lac启动子 - 操纵子控制,以便在有无lac诱导剂的情况下测试它们的诱变作用。结果发现,当诱导产生msDNA - Ec86或Ec73时,对于由移码突变引起的Lac - 突变,从Lac - 到Lac + 的回复频率显著增加,但对于替换突变则增加较少。去除错配碱基对消除了高突变频率,并且单独诱导表达RT不会产生诱变作用。这些结果与马斯及其同事的假设一致,即msDNA中的错配碱基对隔离了细胞错配修复系统,导致移码突变增加。