Bourtayre P, Pizzorni L, Liquier J, Taboury J, Taillandier E, Labarre J F
IARC Sci Publ. 1984(53):227-34.
The B----Z conformational transition of double-stranded poly(dG-dC) induced by various nickel salts (chloride, sulfate, subsulfide, carbonate) has been studied by ultraviolet absorption and circular dichroism. The spectra of the nickel compounds, both free and complexed with DNA, have been obtained in the visible and near infrared regions. In all cases the nickel adopts the hexacoordinated ionic form [Ni(H2O6]2+ and induces the B----Z transition of the nucleic acid at submillimolar concentrations (typically 0.4 mM). The addition to the poly(dG-dC)-poly(dG-dC) of an antitumoral drug, pentaziridinocyclodiphosphathiazene (SOAz), inhibits the B----Z transition even at a ten-fold higher nickel concentration (4 mM). Possible implications for carcinogenesis are discussed.
通过紫外吸收和圆二色性研究了各种镍盐(氯化物、硫酸盐、次硫化物、碳酸盐)诱导的双链聚(dG-dC)的B----Z构象转变。已在可见光和近红外区域获得了游离的和与DNA络合的镍化合物的光谱。在所有情况下,镍都采用六配位离子形式[Ni(H2O6]2+,并在亚毫摩尔浓度(通常为0.4 mM)下诱导核酸的B----Z转变。向聚(dG-dC)-聚(dG-dC)中添加抗肿瘤药物五氮杂环丁烷环二磷噻嗪(SOAz),即使在镍浓度高十倍(4 mM)的情况下也能抑制B----Z转变。讨论了其对致癌作用的可能影响。