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铬将谷胱甘肽和半胱氨酸与DNA交联。

Chromium cross-links glutathione and cysteine to DNA.

作者信息

Borges K M, Wetterhahn K E

机构信息

Department of Biochemistry, Dartmouth Medical School, Hanover, NH 03755.

出版信息

Carcinogenesis. 1989 Nov;10(11):2165-8. doi: 10.1093/carcin/10.11.2165.

Abstract

The formation of chromium-DNA adducts, and chromium-mediated peptide-DNA or amino acid-DNA cross-links was measured after treatment of calf thymus DNA and defined DNA polynucleotides in vitro with potassium dichromate in the presence of glutathione or cysteine. The level of chromium bound to DNA after reaction with chromium(VI) in the presence of glutathione increased with increasing glutathione concentration to a level of approximately 1.4 x 10(-2) chromium per nucleotide. Glutathione and chromium were associated with the DNA in a 1:1 ratio. Reaction of chromium(VI) with DNA in the presence of cysteine led to a maximal level of chromium binding that was 10-fold lower than that measured with glutathione, with 2-4 cysteine bound per chromium. The thiol-chromium-DNA complexes were stable to dialysis at room temperature against diethylenetriaminepentaacetic acid, orthophenanthroline and ethylenediaminetetraacetic acid. However, when the chromium-DNA complexes were dialyzed against ethylenediaminetetraacetic acid at 37 degrees C to chelate bound chromium, equivalent amounts of chromium and thiol were lost from the DNA, suggesting that thiol was associated with the DNA-bound chromium. These results suggest that chromium mediates cross-linking of cysteine and glutathione to DNA, to form glutathione-chromium-DNA and (cysteine)2-4-chromium-DNA complexes. In order to probe the DNA base and sequence specificity of glutathione-chromium-DNA adduct formation, chromium and glutathione binding to polynucleotides of defined composition was determined. Preferential binding of chromium to guanine-containing polynucleotides was observed. These results suggest that the interaction of chromium with thiol-containing amino acids and peptides may be important in chromium genotoxicity, and indicate that the thiol-activated chromium may target guanine bases in DNA.

摘要

在用重铬酸钾在谷胱甘肽或半胱氨酸存在的情况下体外处理小牛胸腺DNA和特定的DNA多核苷酸后,测定了铬-DNA加合物以及铬介导的肽-DNA或氨基酸-DNA交联的形成。在谷胱甘肽存在下与铬(VI)反应后,与DNA结合的铬水平随着谷胱甘肽浓度的增加而增加,达到每核苷酸约1.4×10⁻²铬的水平。谷胱甘肽和铬以1:1的比例与DNA结合。在半胱氨酸存在下铬(VI)与DNA的反应导致铬结合的最大水平比用谷胱甘肽测得的低10倍,每个铬结合2 - 4个半胱氨酸。硫醇-铬-DNA复合物在室温下对二乙烯三胺五乙酸、邻菲罗啉和乙二胺四乙酸的透析稳定。然而,当铬-DNA复合物在37℃下用乙二胺四乙酸透析以螯合结合的铬时,等量的铬和硫醇从DNA中丢失,表明硫醇与DNA结合的铬相关。这些结果表明铬介导半胱氨酸和谷胱甘肽与DNA交联,形成谷胱甘肽-铬-DNA和(半胱氨酸)₂₋₄-铬-DNA复合物。为了探究谷胱甘肽-铬-DNA加合物形成的DNA碱基和序列特异性,测定了铬和谷胱甘肽与特定组成的多核苷酸的结合。观察到铬优先与含鸟嘌呤的多核苷酸结合。这些结果表明铬与含硫醇的氨基酸和肽的相互作用在铬的遗传毒性中可能很重要,并表明硫醇活化的铬可能靶向DNA中的鸟嘌呤碱基。

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