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编码大鼠谷氨酸脱羧酶的cDNA的特性分析。

Characterization of a cDNA coding for rat glutamic acid decarboxylase.

作者信息

Wyborski R J, Bond R W, Gottlieb D I

机构信息

Department of Anatomy and Neurobiology, Washington School of Medicine, St. Louis, MO 63310.

出版信息

Brain Res Mol Brain Res. 1990 Aug;8(3):193-8. doi: 10.1016/0169-328x(90)90016-7.

Abstract

cDNA clones have been isolated for rat glutamic acid decarboxylase (glutamate decarboxylase; EC 4.1.1.15) (GAD) and 3216 bp of the sequence have been determined. This sequence extends the previously reported feline GAD cDNA sequence both in the 5' (67 bp) and 3' (887 bp) directions and contains the polyadenylation signal and tail. The cDNA codes for a 67 kDa mol. wt. protein beginning from the putative initiator methionine found in the feline sequence. Extensive homology to feline GAD was identified at the amino acid level (97% identity) within the coding region. This interspecies homology is high compared to other neurotransmitter synthesizing enzymes and suggests selective pressure to maintain the primary sequence throughout the full length of the protein. Homology is found 5' to the putative initiator methionine. Extensive stretches of homology are also found in the 3' non-coding region. These conserved non-coding regions may play a role in GAD mRNA regulation. The rat cDNA sequence will facilitate investigations into the structure and regulation of the GAD gene.

摘要

已分离出大鼠谷氨酸脱羧酶(谷氨酸脱羧酶;EC 4.1.1.15)(GAD)的cDNA克隆,并测定了3216 bp的序列。该序列在5'端(67 bp)和3'端(887 bp)方向上扩展了先前报道的猫GAD cDNA序列,并包含多聚腺苷酸化信号和尾。该cDNA编码一种67 kDa分子量的蛋白质,起始于在猫序列中发现的假定起始甲硫氨酸。在编码区域内,在氨基酸水平上鉴定出与猫GAD有广泛的同源性(97%同一性)。与其他神经递质合成酶相比,这种种间同源性很高,表明在整个蛋白质全长中维持一级序列存在选择性压力。在假定起始甲硫氨酸的5'端发现了同源性。在3'非编码区域也发现了广泛的同源片段。这些保守的非编码区域可能在GAD mRNA调控中起作用。大鼠cDNA序列将有助于对GAD基因结构和调控的研究。

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