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烷基化鸟嘌呤在哺乳动物细胞中诱导的细胞遗传学效应。

Cytogenetic effects induced by alkylated guanine in mammalian cells.

作者信息

Bonatti S, De Ferrari M, Pisano V, Abbondandolo A

机构信息

Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.

出版信息

Mutagenesis. 1986 Mar;1(2):99-105. doi: 10.1093/mutage/1.2.99.

Abstract

Cytogenetic effects of O6-ethylguanine (O6EtG) were investigated in V79 Chinese hamster cells and human lymphocytes. The frequency of micronuclei and of polyploid cells was increased in a dose-dependent manner in V79 cells. Micronuclei were larger than those induced by the alkylating agent diethylsulfate, suggesting that they originated from chromosome loss rather than from chromosome breakage. Chromosome displacement was also observed and further indicated damage to the spindle. In human lymphocytes, both aneuploidy and polyploidy were induced. O6EtG did not induce either micronuclei or polyploidy in a V79 derivative, deficient in hypoxanthine-guanine phosphoribosyl transferase, suggesting that conversion of the base to a nucleotide is necessary. Preliminary data indicated that 7-ethylguanine was also able to induce aneuploidy and polyploidy in lymphocytes, although it was barely active in V79 cells. The hypothesis proposed is that alkylated nucleotides may behave as spindle poisons. As a consequence, treatment of mammalian cells with alkylating agents may induce numerical chromosome aberrations via alkylation of guanine nucleotide pools, a pathway which has not so far been proposed.

摘要

在V79中国仓鼠细胞和人类淋巴细胞中研究了O6-乙基鸟嘌呤(O6EtG)的细胞遗传学效应。在V79细胞中,微核和多倍体细胞的频率呈剂量依赖性增加。微核比烷化剂硫酸二乙酯诱导产生的微核更大,这表明它们起源于染色体丢失而非染色体断裂。还观察到了染色体移位,进一步表明纺锤体受到了损伤。在人类淋巴细胞中,非整倍体和多倍体均被诱导产生。在缺乏次黄嘌呤-鸟嘌呤磷酸核糖基转移酶的V79衍生物中,O6EtG既不诱导微核也不诱导多倍体,这表明碱基向核苷酸的转化是必要的。初步数据表明,7-乙基鸟嘌呤也能够在淋巴细胞中诱导非整倍体和多倍体,尽管它在V79细胞中几乎没有活性。所提出的假说是,烷基化核苷酸可能表现为纺锤体毒物。因此,用烷化剂处理哺乳动物细胞可能通过鸟嘌呤核苷酸池的烷基化诱导染色体数目畸变,这是一条迄今尚未被提出的途径。

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