Eyler Daniel E, Burnham Kylie A, Wilson Thomas E, O'Brien Patrick J
Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI, United States of America.
Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, United States of America.
PLoS One. 2017 Mar 23;12(3):e0174041. doi: 10.1371/journal.pone.0174041. eCollection 2017.
Human alkyladenine DNA glycosylase (AAG) initiates base excision repair (BER) to guard against mutations by excising alkylated and deaminated purines. Counterintuitively, increased expression of AAG has been implicated in increased rates of spontaneous mutation in microsatellite repeats. This microsatellite mutator phenotype is consistent with a model in which AAG excises bulged (unpaired) bases, altering repeat length. To directly test the role of base excision in AAG-induced mutagenesis, we conducted mutation accumulation experiments in yeast overexpressing different variants of AAG and detected mutations via high-depth genome resequencing. We also developed a new software tool, hp_caller, to perform accurate genotyping at homopolymeric repeat loci. Overexpression of wild-type AAG elevated indel mutations in homopolymeric sequences distributed throughout the genome. However, catalytically inactive variants (E125Q/E125A) caused equal or greater increases in frameshift mutations. These results disprove the hypothesis that base excision is the key step in mutagenesis by overexpressed wild-type AAG. Instead, our results provide additional support for the previously published model wherein overexpressed AAG interferes with the mismatch repair (MMR) pathway. In addition to the above results, we observed a dramatic mutator phenotype for N169S AAG, which has increased rates of excision of undamaged purines. This mutant caused a 10-fold increase in point mutations at G:C base pairs and a 50-fold increase in frameshifts in A:T homopolymers. These results demonstrate that it is necessary to consider the relative activities and abundance of many DNA replication and repair proteins when considering mutator phenotypes, as they are relevant to the development of cancer and its resistance to treatment.
人类烷基腺嘌呤DNA糖基化酶(AAG)启动碱基切除修复(BER),通过切除烷基化和脱氨基嘌呤来防止突变。与直觉相反,AAG表达增加与微卫星重复序列中自发突变率的增加有关。这种微卫星突变体表型与一个模型一致,在该模型中,AAG切除凸起(未配对)的碱基,改变重复长度。为了直接测试碱基切除在AAG诱导的诱变中的作用,我们在过表达不同AAG变体的酵母中进行了突变积累实验,并通过高深度基因组重测序检测突变。我们还开发了一种新的软件工具hp_caller,用于在同聚物重复序列位点进行准确的基因分型。野生型AAG的过表达增加了分布在整个基因组中的同聚物序列中的插入缺失突变。然而,催化无活性的变体(E125Q/E125A)导致移码突变增加相同或更多。这些结果反驳了碱基切除是过表达的野生型AAG诱变关键步骤的假设。相反,我们的结果为先前发表的模型提供了额外支持,即在该模型中,过表达的AAG干扰错配修复(MMR)途径。除上述结果外,我们观察到N169S AAG具有显著的突变体表型,其未受损嘌呤的切除率增加。该突变体导致G:C碱基对处的点突变增加10倍,A:T同聚物中的移码增加50倍。这些结果表明,在考虑突变体表型时,有必要考虑许多DNA复制和修复蛋白的相对活性和丰度,因为它们与癌症的发生及其对治疗的抗性相关。