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Characterization and expression of serotonin transporter genes in zebrafish.

机译:斑马鱼中5-羟色胺转运蛋白基因的表征和表达。

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To understand the development of serotonergic neurons in vertebrates, we used zebrafish as a model system. In this study we cloned two cDNAs (complementary DNAs) coding for serotonin transporter (SERT) from the zebrafish, named serta and sertb. The serta cDNA encodes a protein of 693 amino acids and showed high level of sequence identity with rat and human SERTs. In situ hybridization showed serta to be expressed in raphe nuclei, ventral posterior tuberculum and pineal organ. The expression of serta in raphe and ventral posterior tuberculum overlapped with the location of serotonin and expression of tryptophan hydroxylase, which is a key enzyme for serotonin synthesis. In the pineal organ serta is expressed in the cells in the vicinity of tryptophan hydroxylase-positive cells. We also cloned another zebrafish serotonin transporter, sertb, and found to be expressed in the medulla oblongata and in the inner nuclear layer of retina. The existence of two sert genes in the zebrafish genome indicates the gene was duplicated in the process of evolution as can be seen in other genes in the teleosts including zebrafish. The expression of the serta cDNA in cultured cells conferred a serotonin transport activity, thus indicating the validity of the cloned cDNA. We have established the expression system of zebrafish serotonin transporter in the cell culture in the present study, which is useful for the pharmacological analysis to determine the important residues for the interaction with serotonin and inhibitors. The expression system in the cell culture can be used to determine the effective concentration of inhibitors and addictive drugs. These information might be useful to evaluate the effect of those chemicals on serotonin neuron development and behavior of the animal.
机译:为了了解脊椎动物中血清素能神经元的发育,我们使用斑马鱼作为模型系统。在这项研究中,我们从斑马鱼中克隆了两个编码血清素转运蛋白(SERT)的cDNA(互补DNA),分别称为serta和sertb。 serta cDNA编码一个693个氨基酸的蛋白质,并显示出与大鼠和人SERT的高度序列同一性。原位杂交显示浆膜在缝核,腹后​​结核和松果体器官中表达。缝线和腹侧后结核中的浆膜表达与5-羟色胺的位置和色氨酸羟化酶的表达重叠,色氨酸羟化酶是5-羟色胺合成的关键酶。在松果体器官中,色氨酸羟化酶阳性细胞附近的细胞表达浆膜。我们还克隆了另一种斑马鱼血清素转运蛋白sertb,并发现其在延髓和视网膜内核层表达。斑马鱼基因组中存在两个sert基因,这表明该基因在进化过程中是重复的,正如在硬骨鱼中其他基因(包括斑马鱼)中所看到的那样。 Serta cDNA在培养细胞中的表达赋予血清素转运活性,从而表明克隆的cDNA的有效性。本研究建立了斑马鱼5-羟色胺转运蛋白在细胞培养中的表达系统,可用于药理分析,确定与5-羟色胺和抑制剂相互作用的重要残基。细胞培养物中的表达系统可用于确定抑制剂和成瘾药物的有效浓度。这些信息可能有助于评估这些化学物质对5-羟色胺神经元发育和动物行为的影响。

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