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编码人脑中血清素转运体的cDNA的分离。

Isolation of a cDNA encoding the human brain serotonin transporter.

作者信息

Lesch K P, Wolozin B L, Estler H C, Murphy D L, Riederer P

机构信息

Department of Psychiatry, University of Würzburg, Federal Republic of Germany.

出版信息

J Neural Transm Gen Sect. 1993;91(1):67-72. doi: 10.1007/BF01244919.

Abstract

A cDNA encoding a serotonin transporter (5-HTT) in the human dorsal raphe nucleus was isolated and sequenced using cross-species amplification of human 5-HTT partial cDNA by the polymerase chain reaction (PCR) and the RACE-PCR procedure, designed for rapid amplification of 3' and 5' cDNA ends. The cDNA contains an open reading frame encoding a hydrophobic polypeptide of 630 amino acids with a calculated molecular weight of approximately 70 kDa. The human 5-HTT is approximately 92% homologous to the rat protein but contains an additional consensus phosphorylation site for cAMP-dependent protein kinase recognition located in the cytoplasmic N-terminal region, while a potential protein kinase C phosphorylation site identified in the rat homolog is not conserved in the human 5-HTT. Hydropathicity analysis revealed twelve membrane spanning segments, a topology proposed for other cloned sodium-dependent transporters.

摘要

利用聚合酶链反应(PCR)对人5-羟色胺转运体(5-HTT)部分cDNA进行跨物种扩增,并采用RACE-PCR方法(用于快速扩增cDNA的3'和5'末端),分离并测序了人背缝核中编码5-羟色胺转运体(5-HTT)的cDNA。该cDNA包含一个开放阅读框,编码一个由630个氨基酸组成的疏水多肽,计算分子量约为70 kDa。人5-HTT与大鼠蛋白的同源性约为92%,但在细胞质N端区域含有一个额外的cAMP依赖性蛋白激酶识别的共有磷酸化位点,而在大鼠同源物中鉴定出的一个潜在蛋白激酶C磷酸化位点在人5-HTT中并不保守。亲水性分析揭示了十二个跨膜区段,这是其他克隆的钠依赖性转运体所提出的一种拓扑结构。

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