Kooistra R, Zonneveld J B, Watson A J, Margison G P, Lohman P H, Pastink A
MGC Department of Radiation Genetics and Chemical Mutagenesis, Leiden University Medical Centre, Wassenaarseweg 72, 2333 AL Leiden, The Netherlands.
Nucleic Acids Res. 1999 Apr 15;27(8):1795-801. doi: 10.1093/nar/27.8.1795.
The protein O 6-alkylguanine-DNA alkyltransferase(alkyltransferase) is involved in the repair of O 6-alkylguanine and O 4-alkylthymine in DNA and plays an important role in most organisms in attenuating the cytotoxic and mutagenic effects of certain classes of alkylating agents. A genomic clone encompassing the Drosophila melanogaster alkyltransferase gene ( DmAGT ) was identified on the basis of sequence homology with corresponding genes in Saccharomyces cerevisiae and man. The DmAGT gene is located at position 84A on the third chromosome. The nucleotide sequence of DmAGT cDNA revealed an open reading frame encoding 194 amino acids. The MNNG-hypersensitive phenotype of alkyltransferase-deficient bacteria was rescued by expression of the DmAGT cDNA. Furthermore, alkyltransferase activity was identified in crude extracts of Escherichia coli harbouring DmAGT cDNA and this activity was inhibited by preincubation of the extract with an oligonucleotide containing a single O6-methylguanine lesion. Similar to E.coli Ogt and yeast alkyltransferase but in contrast to the human alkyltransferase, the Drosophila alkyltransferase is resistant to inactivation by O 6-benzylguanine. In an E.coli lac Z reversion assay, expression of DmAGT efficiently suppressed MNNG-induced G:C-->A:T as well as A:T-->G:C transition mutations in vivo. These results demonstrate the presence of an alkyltransferase specific for the repair of O 6-methylguanine and O 4-methylthymine in Drosophila.
蛋白质O 6-烷基鸟嘌呤-DNA烷基转移酶(烷基转移酶)参与DNA中O 6-烷基鸟嘌呤和O 4-烷基胸腺嘧啶的修复,并且在大多数生物体中,在减弱某些种类烷基化剂的细胞毒性和诱变作用方面发挥重要作用。基于与酿酒酵母和人类相应基因的序列同源性,鉴定出一个包含黑腹果蝇烷基转移酶基因(DmAGT)的基因组克隆。DmAGT基因位于第三条染色体的84A位置。DmAGT cDNA的核苷酸序列揭示了一个编码194个氨基酸的开放阅读框。DmAGT cDNA的表达挽救了烷基转移酶缺陷型细菌对MNNG敏感的表型。此外,在含有DmAGT cDNA的大肠杆菌粗提物中鉴定出了烷基转移酶活性,并且这种活性通过用含有单个O6-甲基鸟嘌呤损伤的寡核苷酸对提取物进行预孵育而受到抑制。与大肠杆菌Ogt和酵母烷基转移酶相似,但与人类烷基转移酶不同,果蝇烷基转移酶对O 6-苄基鸟嘌呤的失活具有抗性。在大肠杆菌lac Z回复突变试验中,DmAGT的表达在体内有效抑制了MNNG诱导的G:C→A:T以及A:T→G:C的转换突变。这些结果证明果蝇中存在一种特异性修复O 6-甲基鸟嘌呤和O 4-甲基胸腺嘧啶的烷基转移酶。