Sneider T W, Teague W M, Rogachevsky L M
Nucleic Acids Res. 1975 Oct;2(10):1685-700. doi: 10.1093/nar/2.10.1685.
Partial purification of DNA methylase from Novikoff rat hepatoma cells is described. Contamination with other proteins persists although the enzyme preparation has a high specific activity and is purified 980-fold over homogenate activity. Evidence suggests, but does not prove, that there may be more than one species of DNA methylase in these cells. The enzyme has two broad pH optima at pH 7.0 and 7.5 and most readily methylates heterologous denatured DNAs although complex reaction kinetics indicate that native DNAs may eventually be methylated to an equal or greater level. The preparation of undermethylated DNA from Novikoff cells is also described. Undermethylated homologous DNA is an 85-fold greater acceptor of methyl groups than fully methylated Novikoff cell DNA. In contrast to other DNA substrates, the enzyme preparation methylates native undermethylated homologous DNA at a 3.5-fold greater than denatured undermethylated homologous DNA.
本文描述了从诺维科夫大鼠肝癌细胞中部分纯化DNA甲基化酶的过程。尽管酶制剂具有高比活性,且比匀浆活性纯化了980倍,但仍存在其他蛋白质的污染。有证据表明,但未证实,这些细胞中可能存在不止一种DNA甲基化酶。该酶在pH 7.0和7.5时有两个较宽的pH最佳值,最容易甲基化异源变性DNA,尽管复杂的反应动力学表明天然DNA最终可能被甲基化到相同或更高的水平。本文还描述了从诺维科夫细胞中制备低甲基化DNA的方法。低甲基化的同源DNA作为甲基基团的受体,其接受能力比完全甲基化的诺维科夫细胞DNA高85倍。与其他DNA底物相比,酶制剂对天然低甲基化同源DNA的甲基化作用比对变性低甲基化同源DNA的甲基化作用高3.5倍。