Li J H, Rossman T G
Institute of Environmental Medicine, New York University Medical Center, Tuxedo 10987.
Mol Toxicol. 1989 Winter;2(1):1-9.
We have previously shown that the inhibition of MNU-induced DNA repair by arsenite occurs after the incision step in Chinese hamster V79 cells. We now report that nuclear DNA ligase activity is inhibited after arsenite treatment and that the inhibited activity is mostly DNA ligase II. Both constitutive and MNU-inducible levels of DNA ligase II are inhibited. The addition of arsenite in vitro also indicates that DNA ligase II is more sensitive to arsenite inhibition than DNA ligase I. Since DNA ligase II is reported to be involved in the ligation step of excision repair, its inhibition by arsenite is a likely mechanism for the inhibition of DNA repair by arsenite and may account for the fact that arsenite acts as a comutagen with a number of different types of mutagens. The carcinogenicity of arsenite may also be a result of ligase inhibition.
我们之前已经表明,在中华仓鼠V79细胞中,亚砷酸盐对N-甲基-N-亚硝基脲(MNU)诱导的DNA修复的抑制发生在切口步骤之后。我们现在报告,亚砷酸盐处理后核DNA连接酶活性受到抑制,且被抑制的活性主要是DNA连接酶II。DNA连接酶II的组成型水平和MNU诱导型水平均受到抑制。体外添加亚砷酸盐也表明,DNA连接酶II比亚砷酸盐更敏感。由于据报道DNA连接酶II参与切除修复的连接步骤,其被亚砷酸盐抑制可能是亚砷酸盐抑制DNA修复的一种机制,这可能解释了亚砷酸盐与多种不同类型诱变剂作为共诱变剂的事实。亚砷酸盐的致癌性也可能是连接酶抑制的结果。