Julien J F, Samama P, Mallet J
Laboratoire de Neurobiologie Cellulaire et Moléculaire, Centre National de la Recherche Scientifique, Gif-sur-Yvette, France.
J Neurochem. 1990 Feb;54(2):703-5. doi: 10.1111/j.1471-4159.1990.tb01928.x.
A cDNA clone complementary to the rat brain glutamic acid decarboxylase mRNA was isolated from a rat brain cDNA expression library using an antibody specific to the enzyme. The cDNA insert has been shown to direct the synthesis of an active protein in Escherichia coli. In this study, the nucleotide sequence of this clone, which includes the complete coding region, is presented. The predicted protein is 593 amino acids in length. The first 557 residues display a 95% identity when compared with the corresponding cat sequence. However, the deduced amino acid sequence of the carboxy-terminal end of the rat protein, downstream of residue 557, is totally different from the cat, whereas it agrees with a published partial peptidic sequence of the rat protein.
利用针对该酶的特异性抗体,从大鼠脑cDNA表达文库中分离出与大鼠脑谷氨酸脱羧酶mRNA互补的cDNA克隆。已证明该cDNA插入片段可指导大肠杆菌中活性蛋白的合成。在本研究中,给出了该克隆的核苷酸序列,其中包括完整的编码区。预测的蛋白质长度为593个氨基酸。与相应的猫序列相比,前557个残基显示出95%的同一性。然而,大鼠蛋白羧基末端(第557位残基下游)的推导氨基酸序列与猫的序列完全不同,而与已发表的大鼠蛋白部分肽序列一致。