Moore Jessica M, Correa Raul, Rosenberg Susan M, Hastings P J
Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas, United States of America.
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
PLoS Genet. 2017 Jul 20;13(7):e1006733. doi: 10.1371/journal.pgen.1006733. eCollection 2017 Jul.
Bacteria, yeast and human cancer cells possess mechanisms of mutagenesis upregulated by stress responses. Stress-inducible mutagenesis potentially accelerates adaptation, and may provide important models for mutagenesis that drives cancers, host pathogen interactions, antibiotic resistance and possibly much of evolution generally. In Escherichia coli repair of double-strand breaks (DSBs) becomes mutagenic, using low-fidelity DNA polymerases under the control of the SOS DNA-damage response and RpoS general stress response, which upregulate and allow the action of error-prone DNA polymerases IV (DinB), II and V to make mutations during repair. Pol IV is implied to compete with and replace high-fidelity DNA polymerases at the DSB-repair replisome, causing mutagenesis. We report that up-regulated Pol IV is not sufficient for mutagenic break repair (MBR); damaged bases in the DNA are also required, and that in starvation-stressed cells, these are caused by reactive-oxygen species (ROS). First, MBR is reduced by either ROS-scavenging agents or constitutive activation of oxidative-damage responses, both of which reduce cellular ROS levels. The ROS promote MBR other than by causing DSBs, saturating mismatch repair, oxidizing proteins, or inducing the SOS response or the general stress response. We find that ROS drive MBR through oxidized guanines (8-oxo-dG) in DNA, in that overproduction of a glycosylase that removes 8-oxo-dG from DNA prevents MBR. Further, other damaged DNA bases can substitute for 8-oxo-dG because ROS-scavenged cells resume MBR if either DNA pyrimidine dimers or alkylated bases are induced. We hypothesize that damaged bases in DNA pause the replisome and allow the critical switch from high fidelity to error-prone DNA polymerases in the DSB-repair replisome, thus allowing MBR. The data imply that in addition to the indirect stress-response controlled switch to MBR, a direct cis-acting switch to MBR occurs independently of DNA breakage, caused by ROS oxidation of DNA potentially regulated by ROS regulators.
细菌、酵母和人类癌细胞拥有因应激反应而上调的诱变机制。应激诱导的诱变可能会加速适应性,并且可能为驱动癌症、宿主病原体相互作用、抗生素耐药性以及可能总体上大部分进化的诱变提供重要模型。在大肠杆菌中,双链断裂(DSB)的修复会变得具有诱变性,在SOS DNA损伤反应和RpoS一般应激反应的控制下使用低保真度DNA聚合酶,这些反应会上调并允许易出错的DNA聚合酶IV(DinB)、II和V在修复过程中发挥作用以产生突变。Pol IV被认为在DSB修复复制体处与高保真度DNA聚合酶竞争并取代它们,从而导致诱变。我们报告上调的Pol IV不足以进行诱变断裂修复(MBR);DNA中的受损碱基也是必需的,并且在饥饿应激细胞中,这些是由活性氧(ROS)引起的。首先,ROS清除剂或氧化损伤反应的组成性激活都会降低MBR,这两者都会降低细胞内ROS水平。ROS促进MBR的方式并非通过引起DSB、使错配修复饱和、氧化蛋白质或诱导SOS反应或一般应激反应。我们发现ROS通过DNA中的氧化鸟嘌呤(8-氧代-dG)驱动MBR,因为过量产生一种从DNA中去除8-氧代-dG的糖基化酶会阻止MBR。此外,其他受损的DNA碱基可以替代8-氧代-dG,因为如果诱导DNA嘧啶二聚体或烷基化碱基,ROS清除的细胞会恢复MBR。我们假设DNA中的受损碱基会使复制体暂停,并允许在DSB修复复制体中从高保真度DNA聚合酶关键切换到易出错的DNA聚合酶,从而实现MBR。数据表明,除了间接的应激反应控制的MBR切换外,还存在一种独立于DNA断裂的直接顺式作用的MBR切换,这是由ROS对DNA的氧化引起的,可能受ROS调节因子调控。