Ohta H
Department of Occupational Health and Toxicology, School of Allied Health Science, Kitasato University.
Nihon Rinsho. 1996 Jan;54(1):40-5.
Metallothionein (MT) is low-molecular-weight metal binding proteins with a high cysteine content, which provide the protection against metal toxicity and the regulation of essential trace elements such as zinc and copper. MT is inducible proteins by various metals, hormones, cytokines, and endogenous and exogenous agents. Human MT genes locate on chromosome 16, and mainly three isoforms of MT (MT-I, MT-II, MT-III) have been identified. MT genes expression is controlled mainly at the transcriptional level, and is regulated by the interaction between cis-acting elements (MRE, GRE, IRE) and trans-acting factors (MTF-1, ZRF, MRE-BF-1 and 2, MREBP). Regulation of MT genes by metals may be mediated by MTF-1 interacting with MREs and zinc functions to release MTF-1 from an inhibitor (MTI).
金属硫蛋白(MT)是一类低分子量、富含半胱氨酸的金属结合蛋白,可提供针对金属毒性的保护作用,并调节锌和铜等必需微量元素。MT可被各种金属、激素、细胞因子以及内源性和外源性物质诱导产生。人类MT基因位于16号染色体上,主要已鉴定出三种MT同工型(MT-I、MT-II、MT-III)。MT基因的表达主要在转录水平受到控制,并通过顺式作用元件(MRE、GRE、IRE)与反式作用因子(MTF-1、ZRF、MRE-BF-1和2、MREBP)之间的相互作用进行调节。金属对MT基因的调节可能由MTF-1与MREs相互作用介导,锌则起到将MTF-1从抑制剂(MTI)中释放出来的作用。