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首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Molecular characterization and transcriptional regulation of the sodium-dependent vitamin C transporter genes (slc23a1 and slc23a2) in a teleost fish, the Senegalese sole (Solea senegalensis)
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Molecular characterization and transcriptional regulation of the sodium-dependent vitamin C transporter genes (slc23a1 and slc23a2) in a teleost fish, the Senegalese sole (Solea senegalensis)

机译:塞内加尔唯一的硬骨鱼(Solea senegalensis)中钠依赖性维生素C转运蛋白基因(slc23a1和slc23a2)的分子表征和转录​​调控

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摘要

Vitamin C (ascorbic acid, AA) is an antioxidant that acts as a free radical scavenger and cofactor for several important enzymatic reactions, thus being important for normal cellular functions, growth and development. Accumulation of AA in cells depends on two types of sodium-dependent vitamin C transporters (SVCTs), designed as SVCT1 and SVCT2. In human, they are the products of SLC23A1 and SLC23A2 genes, respectively. In the present work, the molecular cloning of the cDNAs corresponding to slc23a1 and slc23a2 in a teleost fish, the Senegalese sole (Solea senegalensis Kaup, 1858) is first described. Sequence analysis of the predicted polypeptides revealed a conserved topology with those of mammals with important motifs involved in structure and function, being also present in svct1 and svct2. Phylogenetic analyses including a range of vertebrate SVCTs suggest that both transporters are the result of an ancient gene duplication event that occurred prior to the divergence of tetrapods and teleosts, which took place 450. million years ago. Expression profiles in juvenile tissues and during larval development were analyzed using a real-time PCR approach. In juvenile fish, slc23a1 was strongly expressed in intestine, whereas slc23a2 exhibited a widespread distribution in tissues. Transcripts of both genes were detected at early developmental stages, probably representing mRNAs of maternal origin. A possible regulation by their own substrate was detected after first uptakes of AA from diet in both genes. During metamorphosis, both slc23a1 and slc23a2 were down-regulated, the former in a thyroid hormone (TH) dependent way. This pattern coincided with a significant reduction in the AA content of larvae during metamorphosis. These results are interpreted in a physiological context of general reduction in the metabolism of metamorphic larvae. Data presented here provide the first step toward a better understanding of the physiological role of SVCTs in teleost fish.
机译:维生素C(抗坏血酸,AA)是一种抗氧化剂,可作为自由基清除剂和多种重要酶促反应的辅助因子,因此对正常细胞功能,生长和发育至关重要。细胞中AA的积累取决于两种类型的钠依赖性维生素C转运蛋白(SVCT),分别设计为SVCT1和SVCT2。在人类中,它们分别是SLC23A1和SLC23A2基因的产物。在本工作中,首先描述了在硬骨鱼塞内加尔唯一的鱼(Solea senegalensis Kaup,1858年)中对应于slc23a1和slc23a2的cDNA的分子克隆。预测多肽的序列分析揭示了保守的拓扑结构,其中哺乳动物具有重要的结构和功能相关基序,也存在于svct1和svct2中。系统发育分析包括一系列的脊椎动物SVCT,表明这两种转运蛋白都是在四足动物和硬骨鱼发散之前发生的古老基因复制事件的结果,发生于450.百万年前。使用实时PCR方法分析了幼虫组织和幼体发育过程中的表达谱。在幼鱼中,slc23a1在肠道中强烈表达,而slc23a2在组织中表现出广泛的分布。在早期发育阶段都检测到了这两个基因的转录本,可能代表了母亲的mRNA。在两个基因中首次从饮食中摄取AA后,检测到它们自身底物的可能调节。在变态过程中,slc23a1和slc23a2均被下调,前者以甲状腺激素(TH)依赖性方式发生。此模式与变态期间幼虫的AA含量显着降低相吻合。这些结果在变态幼虫的代谢普遍减少的生理环境中得到解释。此处提供的数据为更好地了解硬骨鱼中SVCT的生理作用提供了第一步。

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