Hiraku Y, Yamasaki M, Kawanishi S
Department of Hygiene, Mie University School of Medicine, Tsu, Japan.
FEBS Lett. 1998 Jul 31;432(1-2):13-6. doi: 10.1016/s0014-5793(98)00823-0.
We examined the mechanism of DNA damage induced by a mutagenic tyrosine metabolite, homogentisic acid (HGA), using 32P-5'-end-labeled DNA fragments obtained from the human p53 tumor suppressor gene. HGA caused DNA damage in the presence of Cu(II), particularly at thymine and cytosine residues. Catalase and bathocuproine inhibited the DNA damage, suggesting the involvement of H2O2 and Cu(I). The formation of 8-oxo-7,8-dihydro-2'-deoxyguanosine by HGA increased depending on HGA concentration in the presence of Cu(II). It is concluded that H2O2 is generated during Cu(II)-catalyzed HGA autoxidation and reacts with Cu(I) to form the Cu(I)-peroxide complex, capable of causing oxidative DNA damage.
我们使用从人p53肿瘤抑制基因获得的32P - 5'-末端标记的DNA片段,研究了诱变酪氨酸代谢物尿黑酸(HGA)诱导DNA损伤的机制。在Cu(II)存在下,HGA会导致DNA损伤,尤其是在胸腺嘧啶和胞嘧啶残基处。过氧化氢酶和bathocuproine抑制了DNA损伤,表明H2O2和Cu(I)参与其中。在Cu(II)存在下,HGA形成8-氧代-7,8-二氢-2'-脱氧鸟苷的量随HGA浓度增加而增加。得出的结论是,在Cu(II)催化的HGA自氧化过程中会产生H2O2,其与Cu(I)反应形成能够引起氧化性DNA损伤的Cu(I)-过氧化物复合物。