蓝蟹铜特异金属硫蛋白和镉诱导金属硫蛋白cdna的克隆与测序

Rachel A Syring, Thea Hoexum Brouwer, Marius Brouwer
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引用次数: 57

摘要

金属硫蛋白(MTs)是一种富含半胱氨酸的金属结合蛋白,存在于微生物、植物和所有无脊椎动物和脊椎动物中。单细胞真核生物如酵母具有铜- mt,其合成是由铜激活的转录因子诱导的。大多数高等生物有两种主要的镉/锌MT异构体,其合成由锌激活的转录因子控制。蓝蟹(Callinectes sapidus)有两种镉诱导的同种异构体CdMT-I和CdMT-II,还有第三种同种异构体CuMT-II,它由铜诱导,但不受镉诱导。利用cDNA末端的3′和5′快速扩增(RACE)确定铜特异性MT的cDNA序列,以及两个cdmt的cDNA序列。CuMT-II cDNA编码含有21个半胱氨酸残基的63个氨基酸的蛋白。CdMT-I和CdMT-II cDNA分别编码58和57个氨基酸的蛋白质,每个蛋白质含有18个半胱氨酸。分子系统发育分析表明,CdMT亚型与其他甲壳类CdMT聚集在一起,而铜特异性MT与软体动物的MT更接近。CuMT-II与蜗牛Helix pomatia的铜特异性非镉诱导MT具有相当的同源性。在软体动物和甲壳类动物中存在铜特异性mt,这两种动物都依赖于血青素进行氧运输,这表明CuMT-II参与了与血青素合成和降解相关的铜稳态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cloning and sequencing of cDNAs encoding for a novel copper-specific metallothionein and two cadmium-inducible metallothioneins from the blue crab Callinectes sapidus

Metallothioneins (MTs) are cysteine-rich metal-binding proteins found in micro-organisms, plants and all invertebrate and vertebrate animals. Unicellular eukaryotes such as yeast have a copper-MT whose synthesis is induced by a copper-activated transcription factor. Most higher organisms have two major cadmium/zinc MT isoforms, whose synthesis is controlled by a zinc-activated transcription factor. The blue crab, Callinectes sapidus, has two cadmium-inducible isoforms, CdMT-I and CdMT-II, and a third isoform, CuMT-II, which is induced by copper, but not by cadmium. The cDNA sequence of the copper-specific MT, along with those of the two CdMTs, was determined utilizing 3′ and 5′ rapid amplification of cDNA ends (RACE). CuMT-II cDNA encodes a 63 amino acid protein containing 21 cysteine residues. CdMT-I and CdMT-II cDNA encode a 58 and 57 amino acid protein, respectively, each with 18 cysteines. Molecular phylogeny analysis shows that the CdMT isoforms cluster with other crustacean CdMTs, whereas the copper-specific MT is more closely related to mollusk MTs. CuMT-II shows considerable homology to a copper-specific, non-cadmium inducible, MT from the snail, Helix pomatia. The presence of copper-specific MTs in mollusks and crustaceans, both of which are dependent on hemocyanin for oxygen transport, suggests that CuMT-II is involved in copper homeostasis associated with the synthesis and degradation of hemocyanin.

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