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门克斯病:响应铜的异常金属硫蛋白基因调控。

Menkes' disease: abnormal metallothionein gene regulation in response to copper.

作者信息

Leone A, Pavlakis G N, Hamer D H

出版信息

Cell. 1985 Feb;40(2):301-9. doi: 10.1016/0092-8674(85)90144-8.

Abstract

Menkes' disease, an inherited disorder of copper metabolism, is characterized by the accumulation of excess copper-metallothionein in certain tissues and cell types. Using cultured fibroblasts, we show that this is due to the ability of low concentrations of copper to induce metallothionein mRNA synthesis in Menkes' but not normal cells. We also show that copper, which is unusually toxic to Menkes' cells, induces the synthesis of 84 kd and 68 kd polypeptides tentatively identified as heat shock proteins. Transfection experiments with a cloned metallothionein fusion gene show that this is due to a defect in a diffusible factor involved in either metallothionein gene transcriptional regulation or copper metabolism.

摘要

门克斯病是一种遗传性铜代谢紊乱疾病,其特征是在某些组织和细胞类型中积累过量的铜 - 金属硫蛋白。利用培养的成纤维细胞,我们发现这是由于低浓度铜能够在门克斯病细胞而非正常细胞中诱导金属硫蛋白mRNA合成。我们还表明,对门克斯病细胞具有异常毒性的铜会诱导合成暂时鉴定为热休克蛋白的84 kd和68 kd多肽。用克隆的金属硫蛋白融合基因进行的转染实验表明,这是由于参与金属硫蛋白基因转录调控或铜代谢的一种可扩散因子存在缺陷所致。

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