D'Errico Mariarosaria, Parlanti Eleonora, Dogliotti Eugenia
Department of Environment and Primary Prevention, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.
Mutat Res. 2008 Jul-Aug;659(1-2):4-14. doi: 10.1016/j.mrrev.2007.10.003. Epub 2007 Oct 26.
Since DNA is prone to oxidative attack cells have evolved multiple protective strategies to prevent the deleterious effects of DNA oxidation. Base excision repair is the major mechanism for repair of DNA base damage by reactive oxygen species but recent evidence indicate that nucleotide excision repair proteins, that are mutated in human syndromes, are involved too. The mechanisms of repair dealing with the direct oxidation of DNA will be reviewed taking as prototype the oxidized base 7,8-dihydro-8-hydroxyguanine. The function of the individual repair components as inferred from model mice indicate that the ablation of two gene functions is mostly required to lead to accumulation of oxidative DNA damage, mutagenesis and cancer development. The recent identification of human diseases associated with mutations in oxidative damage repair show that defects in this pathway may lead to increased cancer but their major causative role seems to be in neurological diseases.
由于DNA容易受到氧化攻击,细胞已经进化出多种保护策略来防止DNA氧化的有害影响。碱基切除修复是修复活性氧引起的DNA碱基损伤的主要机制,但最近的证据表明,在人类综合征中发生突变的核苷酸切除修复蛋白也参与其中。将以氧化碱基7,8 - 二氢 - 8 - 羟基鸟嘌呤为原型,综述处理DNA直接氧化的修复机制。从模型小鼠推断出的各个修复成分的功能表明,大多需要消除两种基因功能才能导致氧化DNA损伤的积累、诱变和癌症发展。最近鉴定出与氧化损伤修复突变相关的人类疾病,表明该途径的缺陷可能导致癌症增加,但它们的主要致病作用似乎在于神经疾病。