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金属-多核苷酸相互作用。体外致癌金属与非致癌金属的比较。

Metal-polynucleotide interactions. A comparison of carcinogenic and non-carcinogenic metals in vitro.

作者信息

Murray M J, Flessel C P

出版信息

Biochim Biophys Acta. 1976 Mar 4;425(2):256-61. doi: 10.1016/0005-2787(76)90032-0.

DOI:10.1016/0005-2787(76)90032-0
PMID:1252503
Abstract

The effects of divalent cations on mixing curves of synthetic polyribonucleotides in solution are described. Manganese and cadmium chlorides at 10(-3) M induce changes suggestive of base mispairing. MnCl2 induces mispairing in complexes formed between both poly(I) and poly(C,U) and poly(I) and poly(C,A) while CdCl2 affects base pairing between poly(I) and poly(C,U) only. By contrast, the chlorides of magnesium and zinc show no mispairing effects with either polymer pair. Manganese and cadmium are both reported carcinogens in animals while magnesium and zinc are not. The possibility that direct metal-nucleic acid interaction may be involved in metal carcinogenesis is discussed.

摘要

描述了二价阳离子对溶液中合成聚核糖核苷酸混合曲线的影响。10⁻³M的氯化锰和氯化镉会引起一些变化,表明存在碱基错配。氯化锰在聚(I)与聚(C,U)以及聚(I)与聚(C,A)形成的复合物中诱导错配,而氯化镉仅影响聚(I)与聚(C,U)之间的碱基配对。相比之下,氯化镁和氯化锌对这两种聚合物对均未显示错配效应。锰和镉在动物中均被报道为致癌物,而镁和锌则不是。讨论了直接的金属 - 核酸相互作用可能参与金属致癌作用的可能性。

相似文献

1
Metal-polynucleotide interactions. A comparison of carcinogenic and non-carcinogenic metals in vitro.金属-多核苷酸相互作用。体外致癌金属与非致癌金属的比较。
Biochim Biophys Acta. 1976 Mar 4;425(2):256-61. doi: 10.1016/0005-2787(76)90032-0.
2
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Biopolymers. 1973 Nov;12(11):2459-75. doi: 10.1002/bip.1973.360121103.
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The binding of Mg(II) and Ni(II) to synthetic polynucleotides.镁(II)和镍(II)与合成多核苷酸的结合。
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Raman spectroscopy of DNA-metal complexes. II. The thermal denaturation of DNA in the presence of Sr2+, Ba2+, Mg2+, Ca2+, Mn2+, Co2+, Ni2+, and Cd2+.DNA-金属络合物的拉曼光谱。II. Sr2+、Ba2+、Mg2+、Ca2+、Mn2+、Co2+、Ni2+和Cd2+存在下DNA的热变性
Biophys J. 1995 Dec;69(6):2623-41. doi: 10.1016/S0006-3495(95)80133-5.
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A thermodynamic analysis of the influence of simple mono-and divalent cations on the conformational transitions of polynucleotide complexes.简单单价和二价阳离子对多核苷酸复合物构象转变影响的热力学分析。
Biochemistry. 1974 Jun 4;13(12):2579-89. doi: 10.1021/bi00709a017.
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Effects of essential divalent metals on carcinogenicity and metabolism of nickel and cadmium.必需二价金属对镍和镉致癌性和代谢的影响。
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In vitro inhibition of aryl hydrocarbon hydroxylase by heavy metals.重金属对芳烃羟化酶的体外抑制作用。
Oncology. 1976;33(5-6):201-4. doi: 10.1159/000225144.

引用本文的文献

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Mechanisms of metal carcinogenesis.金属致癌的机制。
Biol Trace Elem Res. 1979 Mar;1(1):63-86. doi: 10.1007/BF02783844.
2
DNA polymerase mu (Pol mu), homologous to TdT, could act as a DNA mutator in eukaryotic cells.与末端脱氧核苷酸转移酶(TdT)同源的DNA聚合酶μ(Pol μ)可在真核细胞中充当DNA诱变剂。
EMBO J. 2000 Apr 3;19(7):1731-42. doi: 10.1093/emboj/19.7.1731.
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In Vitro models and methods for bioassay and studies of cellular mechanisms.用于生物测定和细胞机制研究的体外模型和方法。
Environ Health Perspect. 1981 Aug;40:35-42. doi: 10.1289/ehp.40-1568812.
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Metal-induced infidelity of DNA synthesis.金属诱导的DNA合成错误
Environ Health Perspect. 1981 Aug;40:197-205. doi: 10.1289/ehp.8140197.
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Metal-induced infidelity of DNA synthesis.金属诱导的DNA合成错误
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