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首页> 外文期刊>Comparative biochemistry and physiology. Toxicology & pharmacology: CBP >Molecular cloning and expression study of pi-class glutathione S-transferase (pi-GST) and selenium-dependent glutathione peroxidase (Se-GPx) transcripts in the freshwater bivalve Dreissena polymorpha
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Molecular cloning and expression study of pi-class glutathione S-transferase (pi-GST) and selenium-dependent glutathione peroxidase (Se-GPx) transcripts in the freshwater bivalve Dreissena polymorpha

机译:淡水双壳贝母Dreissena polymorpha中pi类谷胱甘肽S-转移酶(pi-GST)和硒依赖性谷胱甘肽过氧化物酶(Se-GPx)转录本的分子克隆和表达研究

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摘要

Glutathione S-transferases (GST) and glutathione peroxidases (GPx) are essential components of cellular detoxification systems. We identified GST and GPx transcripts in the freshwater bivalve Dreissena polymorpha, their full-length coding sequences were obtained by reverse-transcription PCR using degenerated primers followed by 5′ and 3′ RACE-PCR (rapid amplification of cDNA ends-PCR). The cDNA identified encoded proteins of 205 and 243 amino acids corresponding respectively to a pi-class GST and a selenium-dependent GPx. The comparison of the deduced amino acid sequences with GST and GPx from other species showed that the residues essential to the enzymatic function of these two proteins are highly conserved. We studied their expression pattern in the digestive gland, the gills and the excretory system of D. polymorpha. The results showed that pi-GST mRNA expression is higher in the digestive gland than in the gills or the excretory system. Se-GPx transcripts are expressed at high, medium and very low levels in the digestive gland, the excretory system and the gills, respectively.
机译:谷胱甘肽S-转移酶(GST)和谷胱甘肽过氧化物酶(GPx)是细胞排毒系统的重要组成部分。我们在淡水双壳贝母Dreissena polymorpha中鉴定了GST和GPx转录本,它们的全长编码序列是通过使用简并引物进行逆转录PCR,然后进行5'和3'RACE-PCR(cDNA末端PCR的快速扩增)而获得的。 cDNA鉴定出205个和243个氨基酸的编码蛋白,分别对应于pi类GST和硒依赖性GPx。推导的氨基酸序列与其他物种的GST和GPx的比较表明,这两种蛋白的酶功能必不可少的残基是高度保守的。我们研究了它们在D. polymorpha的消化腺,the和排泄系统中的表达模式。结果表明,pi-GST mRNA在消化腺中的表达高于the或排泄系统。 Se-GPx转录本分别在消化腺,排泄系统和ill中高,中和非常低的水平表达。

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