Kladova O A, Kuznetsov N A, Fedorova O S
Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090 Russia.
Mol Biol (Mosk). 2021 Mar-Apr;55(2):194-209. doi: 10.31857/S0026898421020087.
In mammalian cells, base excision repair (BER) is the main pathway responsible for the correction of a variety of chemically modified DNA bases. DNA packaging in chromatin affects the accessibility of damaged sites to the enzymes involved in repair processes. This review presents data concerning the enzymes involved in BER. Within the nucleosome core particle (NCP), the accessibility of damaged DNA to enzymes is hindered by the presence of a histone octamer. This means that the removal of DNA lesions largely depends on their rotational and translational positioning in the NCP, as well as on the specific features of each enzyme.
在哺乳动物细胞中,碱基切除修复(BER)是负责纠正多种化学修饰DNA碱基的主要途径。染色质中的DNA包装会影响受损位点对修复过程中所涉及酶的可及性。本综述展示了有关参与碱基切除修复的酶的数据。在核小体核心颗粒(NCP)内,受损DNA对酶的可及性会因组蛋白八聚体的存在而受阻。这意味着DNA损伤的去除很大程度上取决于它们在核小体核心颗粒中的旋转和平移定位,以及每种酶的特定特性。