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酵母金属硫蛋白在金属离子解毒中的作用。

Yeast metallothionein function in metal ion detoxification.

作者信息

Ecker D J, Butt T R, Sternberg E J, Neeper M P, Debouck C, Gorman J A, Crooke S T

出版信息

J Biol Chem. 1986 Dec 25;261(36):16895-900.

PMID:3536930
Abstract

A genetic approach was taken to test the function of yeast metallothionein in metal ion detoxification. A yeast strain was constructed in which the metallothionein locus was deleted (cup1 delta). The cup1 delta strain was complemented with normal or mutant metallothionein genes under normal or constitutive regulatory control on high copy episomal plasmids. Metal resistance of the cup1 delta strain with and without the metallothionein-expressing vectors was analyzed. The normally regulated metallothionein gene conferred resistance only to copper (1000-fold); constitutively expressed metallothionein conferred resistance to both copper (500-fold) and cadmium (1000-fold), but not to mercury, zinc, silver, cobalt, nickel, gold, platinum, lanthanum, uranium, or tin. Two mutant versions of the metallothionein gene were constructed and tested for their ability to confer metal resistance in the cup1 delta background. The first had a deletion of a highly conserved amino acid sequence (Lys-Lys-Ser-Cys-Cys-Ser). The second was a hybrid gene consisting of the sequences coding for the first 20 amino acids of the yeast protein fused to the monkey metallothionein gene. Expression of these genes under the CUP1 promoter provided significant protection from copper, but none of the other metals tested. These results demonstrate that there is significant flexibility in the structural requirements for metallothionein to function in copper detoxification and that yeast metallothionein is also capable of detoxifying cadmium under conditions of constitutive expression.

摘要

采用遗传学方法来测试酵母金属硫蛋白在金属离子解毒中的功能。构建了一个缺失金属硫蛋白基因座(cup1δ)的酵母菌株。在高拷贝附加体质粒上,在正常或组成型调控下,用正常或突变的金属硫蛋白基因对cup1δ菌株进行互补。分析了携带和不携带金属硫蛋白表达载体的cup1δ菌株的金属抗性。正常调控的金属硫蛋白基因仅赋予对铜的抗性(1000倍);组成型表达的金属硫蛋白赋予对铜(500倍)和镉(1000倍)的抗性,但对汞、锌、银、钴、镍、金、铂、镧、铀或锡没有抗性。构建了金属硫蛋白基因的两个突变体版本,并测试它们在cup1δ背景下赋予金属抗性的能力。第一个缺失了一个高度保守的氨基酸序列(Lys-Lys-Ser-Cys-Cys-Ser)。第二个是一个杂合基因,由编码酵母蛋白前20个氨基酸的序列与猴金属硫蛋白基因融合而成。这些基因在CUP1启动子下的表达提供了对铜的显著保护,但对所测试的其他金属均无保护作用。这些结果表明,金属硫蛋白在铜解毒中发挥作用的结构要求具有显著的灵活性,并且酵母金属硫蛋白在组成型表达条件下也能够解除镉的毒性。

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