Ripley L S, Drake J W
Mutat Res. 1984 Nov;129(2):149-52. doi: 10.1016/0027-5107(84)90147-7.
Bisulfite-induced deamination of cytosine produces uracil, a thymine analog reported to be mutagenic both in vitro and in vivo. Although deamination of cytosine in DNA should produce G:C----A:T transitions, treating bacteriophage T4 particles with 0.9 M bisulfite at pH 5 at 37 degrees C produced no more mutations than did the equivalent buffer without bisulfite. Lack of bisulfite mutagenicity is fully consistent with the reported resistance of 5-substituted cytosines to bisulfite-induced deamination, since T4 DNA contains glucosylated 5-hydroxymethylcytosine. However, bisulfite also failed to induce mutations in T4 particles whose DNA contained unmodified cytosine. The lack of mutagenesis persisted in E. coli hosts deficient in uracil glycosylase, an enzyme expected to participate in the repair of the putative bisulfite-generated uracil. Cytosine in T4 DNA may be largely protected from bisulfite attack within phage particles.
亚硫酸氢盐诱导的胞嘧啶脱氨基作用会产生尿嘧啶,尿嘧啶是一种胸腺嘧啶类似物,据报道在体外和体内都具有致突变性。虽然DNA中的胞嘧啶脱氨基作用应该会产生G:C到A:T的转变,但在37℃下用pH值为5的0.9 M亚硫酸氢盐处理噬菌体T4颗粒所产生的突变并不比不含亚硫酸氢盐的等效缓冲液多。亚硫酸氢盐缺乏致突变性与报道的5-取代胞嘧啶对亚硫酸氢盐诱导的脱氨基作用的抗性完全一致,因为T4 DNA含有糖基化的5-羟甲基胞嘧啶。然而,亚硫酸氢盐也未能在其DNA含有未修饰胞嘧啶的T4颗粒中诱导突变。在缺乏尿嘧啶糖基化酶的大肠杆菌宿主中,这种诱变作用的缺乏依然存在,尿嘧啶糖基化酶是一种预期参与修复假定的亚硫酸氢盐产生的尿嘧啶的酶。T4 DNA中的胞嘧啶在噬菌体颗粒内可能很大程度上受到保护,免受亚硫酸氢盐的攻击。