Kamiya Hiroyuki, Tsuchiya Hiroyuki, Karino Naoko, Ueno Yoshihito, Matsuda Akira, Harashima Hideyoshi
Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nishi-6, Kita-ku, Sapporo 060-0812, Japan.
J Biochem. 2002 Oct;132(4):551-5. doi: 10.1093/oxfordjournals.jbchem.a003256.
To examine the mutagenicity of 5-formylcytosine (5-fC), an oxidation product of 5-methylcytosine (5-mC), 5-fC was incorporated into predetermined sites of double-stranded shuttle vectors. The nucleotide sequences in which the modified base was incorporated were 5'-AFGCGT-3' and 5'-ACGFGT-3' (F represents 5-fC), the recognition site for the restriction enzyme MluI (5'-ACGCGT-3'). 5-fC was incorporated into the template strand of either the leading or lagging strand of DNA replication. The modified DNAs were transfected into simian COS-7 cells, and the DNAs replicated in the cells were recovered and analyzed after a second transfection into Escherichia coli. 5-fC weakly blocked DNA replication in mammalian cells. The 5-fC residues were mutagenic, with mutation frequencies in double-stranded vectors of 0.03-0.28%. The mutation spectrum of 5-fC was broad, and included targeted (5-fC-->G, 5-fC-->A, and 5-fC-->T) and untargeted mutations. These results suggest that the oxidation of 5-mC results in mutations at and around the modified sites.
为检测5-甲基胞嘧啶(5-mC)的氧化产物5-甲酰基胞嘧啶(5-fC)的致突变性,将5-fC掺入双链穿梭载体的预定位点。掺入修饰碱基的核苷酸序列为5'-AFGCGT-3'和5'-ACGFGT-3'(F代表5-fC),这是限制性内切酶MluI(5'-ACGCGT-3')的识别位点。5-fC被掺入DNA复制的前导链或后随链的模板链中。将修饰后的DNA转染到猴COS-7细胞中,在细胞中复制的DNA在再次转染到大肠杆菌后回收并进行分析。5-fC在哺乳动物细胞中对DNA复制有微弱的阻断作用。5-fC残基具有致突变性,双链载体中的突变频率为0.03-0.28%。5-fC的突变谱很广,包括靶向突变(5-fC→G、5-fC→A和5-fC→T)和非靶向突变。这些结果表明,5-mC的氧化会导致修饰位点及其周围发生突变。