Bricteux-Grégoire S, Liuzzi M, Talpaert-Borlé M, Winand M, Verly W G
Biochim Biophys Acta. 1986 May 27;867(1-2):24-30. doi: 10.1016/0167-4781(86)90025-4.
Using [32P]DNA alkylated with [3H]methyl methanesulfonate, depurinated by heating at 50 degrees C for various periods, then treated with sodium hydroxide, a table was constructed giving the DNA fraction soluble in 5% perchloric acid at 0 degree C as a function of the frequency of strand breaks. The alkaline treatment placed a break near each apurinic site; the apurinic sites were counted in two ways which gave consonant results: by the loss of [3H]methyl groups and by reaction with [14C]methoxyamine. The 32P label of DNA was used to measure the acid-solubility.
使用用[3H]甲磺酸甲酯烷基化的[32P]DNA,通过在50℃加热不同时间使其脱嘌呤,然后用氢氧化钠处理,构建了一个表格,给出了在0℃下可溶于5%高氯酸的DNA部分随链断裂频率的变化情况。碱性处理在每个脱嘌呤位点附近产生一个断裂;脱嘌呤位点通过两种方式计数,结果一致:通过[3H]甲基的损失以及与[14C]甲氧基胺的反应。DNA的32P标记用于测量酸溶性。