Hardy T A, Baker D J, Newman E M, Sowers L C, Goodman M F, Smith S S
Biochem Biophys Res Commun. 1987 May 29;145(1):146-52. doi: 10.1016/0006-291x(87)91299-x.
M13 DNAs in which carbon 5 of each deoxycytidine residue in one strand is replaced with a bulky group are very good substrates for human DNA (cytosine-5) methyltransferase. Rate enhancements of up to 35 fold are obtained depending on the size of the moiety at C-5. The enzyme appears optimally suited to sense a methyl group in one strand at this position. Alkaline density gradient analyses of the distribution of methyl groups applied to 5-BrdCyd or 5-IdCyd substituted DNA reveal that these groups serve to direct the enzyme to methylate the unsubstituted strand.
在一条链中每个脱氧胞苷残基的碳5被一个庞大基团取代的M13 DNA是人类DNA(胞嘧啶-5)甲基转移酶的非常好的底物。根据C-5处部分的大小,可获得高达35倍的速率增强。该酶似乎最适合在该位置识别一条链中的甲基基团。对应用于5-溴脱氧胞苷或5-碘脱氧胞苷取代DNA的甲基分布进行碱性密度梯度分析表明,这些基团有助于引导该酶使未取代的链甲基化。