Kim S R, Matsui K, Yamada M, Gruz P, Nohmi T
Mol Genet Genomics. 2001 Oct;266(2):207-15. doi: 10.1007/s004380100541.
DNA polymerase IV (pol IV) in Escherichia coli is a member of a novel family of DNA polymerases (the DinB/UmuC/Rad30/Rev1 super-family or the DNA polymerase Y family). Although expression of the dinB gene encoding DNA pol IV is known to result in an enhancement of untargeted mutagenesis, it remains uncertain whether DNA pol IV is involved in a variety of lesion-induced mutagenesis (targeted mutagenesis), and the relationship between expression levels of dinB and the mutagenesis that DNA pol IV promotes has not been investigated thoroughly. Here, we report that DNA pol IV is involved in -1 frameshift mutagenesis induced by 4-nitroquinoline N-oxide (4-NQO) and that the expression level of the chromosomal pol IV gene is 6-12 times higher than those for other SOS-inducible DNA polymerases in E. coli, i.e., DNA pol II (PolB) or DNA pol V (UmuDC), respectively. Interestingly, the dinB gene is present not only on the chromosome but also on the F' plasmid in the E. coli CC108 strain. In this strain, 750 molecules of DNA pol IV are expressed from the F' dinB gene in the uninduced state and 250 molecules are expressed from the chromosomal gene. These cellular expression levels strongly affect -1 frameshifts induced by 4-NQO in runs of six guanine bases: mutagenicity was highest in the strain CC108, followed by strains YG2242 (chromosome deltadinB/F' dinB+), YG2247 (chromosome dinB+/F' deltadinB) and FC1243 (chromosome deltadinB/F' deltadinB). The incidence of untargeted -1 frameshifts was reduced by two-thirds on deletion of dinB from the F' episome. The chromosomal dinB gene appeared to have little or no effect on the untargeted mutagenesis. These results suggest that DNA pol IV efficiently mediates targeted mutagenesis by 4-NQO, and that the cellular levels of expression substantially affect targeted and untargeted mutagenesis.
大肠杆菌中的DNA聚合酶IV(pol IV)是一类新型DNA聚合酶家族(DinB/UmuC/Rad30/Rev1超家族或DNA聚合酶Y家族)的成员。虽然已知编码DNA pol IV的dinB基因的表达会导致非靶向诱变增强,但DNA pol IV是否参与多种损伤诱导的诱变(靶向诱变)仍不确定,并且dinB的表达水平与DNA pol IV促进的诱变之间的关系尚未得到充分研究。在此,我们报告DNA pol IV参与了4-硝基喹啉N-氧化物(4-NQO)诱导的-1移码诱变,并且染色体pol IV基因的表达水平分别比大肠杆菌中其他SOS诱导型DNA聚合酶即DNA聚合酶II(PolB)或DNA聚合酶V(UmuDC)的表达水平高6至12倍。有趣的是,dinB基因不仅存在于染色体上,还存在于大肠杆菌CC108菌株的F'质粒上。在该菌株中,750个DNA pol IV分子在未诱导状态下从F' dinB基因表达,250个分子从染色体基因表达。这些细胞表达水平强烈影响六个鸟嘌呤碱基序列中由4-NQO诱导的-1移码:在CC108菌株中诱变性最高,其次是YG2242菌株(染色体deltadinB/F' dinB +)、YG2247菌株(染色体dinB +/F' deltadinB)和FC1243菌株(染色体deltadinB/F' deltadinB)。从F'附加体中缺失dinB后,非靶向-1移码的发生率降低了三分之二。染色体dinB基因似乎对非靶向诱变几乎没有影响。这些结果表明,DNA pol IV有效地介导了4-NQO诱导的靶向诱变,并且细胞表达水平在很大程度上影响靶向和非靶向诱变。