Institute of Chemical Biology and Fundamental Medicine, Siberian Division of the Russian Academy of Sciences, Novosibirsk, Russia.
Biochemistry (Mosc). 2011 Jan;76(1):80-93. doi: 10.1134/s000629791101010x.
Base excision DNA repair is necessary for removal of damaged nucleobases from the genome and their replacement with normal nucleobases. Base excision repair is initiated by DNA glycosylases, the enzymes that cleave the N-glycosidic bonds of damaged deoxynucleotides. Until recently, only eight DNA glycosylases with different substrate specificity were known in human cells. In 2002, three new human DNA glycosylases (NEIL1, NEIL2, and NEIL3) were discovered, all homologous to endonuclease VIII, a bacterial protein, which also participates in DNA repair. The role of these enzymes remains mostly unknown. In this review we discuss recent data on the substrate specificity of the NEIL enzymes, their catalytic mechanism, structure, interactions with other components of DNA repair system, and possible biological role in preventing diseases associated with DNA damage.
碱基切除修复是从基因组中去除受损碱基并将其替换为正常碱基所必需的。碱基切除修复由 DNA 糖苷酶启动,这些酶能切断受损脱氧核苷酸的 N-糖苷键。直到最近,人们才在人类细胞中发现了 8 种具有不同底物特异性的 DNA 糖苷酶。2002 年,人们发现了三种新的人类 DNA 糖苷酶(NEIL1、NEIL2 和 NEIL3),它们都与内切核酸酶 VIII 同源,后者是一种参与 DNA 修复的细菌蛋白。这些酶的作用仍知之甚少。在这篇综述中,我们讨论了关于 NEIL 酶的底物特异性、催化机制、结构、与 DNA 修复系统其他成分的相互作用以及在预防与 DNA 损伤相关疾病方面的可能生物学作用的最新数据。