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门克斯综合征中金属硫蛋白基因的调控

Metallothionein gene regulation in Menkes' syndrome.

作者信息

Hamer D H

机构信息

Laboratory of Biochemistry, National Cancer Institute, Bethesda, Md 20892.

出版信息

Arch Dermatol. 1987 Oct;123(10):1384a-1385a.

PMID:3662572
Abstract

The characteristic feature of Menkes' disease is a maldistribution of bodily copper; decreased copper levels are present in the serum, brain, and liver, whereas excess levels are present in gut, kidney, and most other nonhepatic tissues. Using cultured fibroblasts, we have shown that low extracellular copper concentrations induce synthesis of metallothionein, a copper-binding protein, in Menkes' cells but not in normal cells. This is due to a defect in a diffusable regulatory factor that is probably involved in copper metabolism. To further understand the role of the defective factor in transcription, assays have been developed to study the metal-dependent binding of nuclear proteins to metallothionein gene control sequences.

摘要

门克斯病的特征是体内铜分布不均;血清、大脑和肝脏中的铜水平降低,而肠道、肾脏和大多数其他非肝脏组织中的铜水平过高。我们利用培养的成纤维细胞表明,低细胞外铜浓度可诱导门克斯病细胞而非正常细胞合成金属硫蛋白(一种铜结合蛋白)。这是由于一种可能参与铜代谢的可扩散调节因子存在缺陷。为了进一步了解缺陷因子在转录中的作用,已开发出检测方法来研究核蛋白与金属硫蛋白基因控制序列的金属依赖性结合。

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