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编码人髓鞘/少突胶质细胞糖蛋白的cDNA的鉴定与表达

Characterization and expression of the cDNA coding for the human myelin/oligodendrocyte glycoprotein.

作者信息

Pham-Dinh D, Allinquant B, Ruberg M, Della Gaspera B, Nussbaum J L, Dautigny A

机构信息

Laboratoire de Neurogénétique Moléculaire, URA 1488, CNRS, Université de Paris VI, France.

出版信息

J Neurochem. 1994 Dec;63(6):2353-6. doi: 10.1046/j.1471-4159.1994.63062353.x.

Abstract

We report here the characterization of a full-length cDNA encoding the human myelin/oligodendrocyte glycoprotein (MOG). The sequence of the coding region of the human MOG cDNA is highly homologous to that of other previously cloned mouse, rat, and bovine MOG cDNAs, but the 3' untranslated region differs by an insertion of an Alu sequence between nucleotides 1,590 and 1,924. Accordingly, northern blot analyzes with cDNA probes corresponding to the coding region or the 3' untranslated Alu-containing sequence revealed a single band of 2 kb, rather than the 1.6 kb of bovine, rat, or mouse MOG cDNA(s). Immunocytochemical analysis of HeLa cells transfected with human MOG cDNA, which was performed using a specific antibody raised against whole MOG, clearly indicated that MOG is expressed at the cell surface as an intrinsic protein. These data are in accordance with the predicted amino acid sequence, which contains a signal peptide and two putative transmembrane domains. The knowledge of the human MOG sequence should facilitate further investigations on its potential as a target antigen in autoimmune demyelinating diseases like multiple sclerosis.

摘要

我们在此报告编码人髓鞘/少突胶质细胞糖蛋白(MOG)的全长cDNA的特征。人MOG cDNA编码区的序列与其他先前克隆的小鼠、大鼠和牛的MOG cDNA高度同源,但3'非翻译区在核苷酸1590至1924之间插入了一段Alu序列,存在差异。因此,用对应于编码区或含3'非翻译Alu序列的cDNA探针进行的Northern印迹分析显示出一条2 kb的条带,而不是牛、大鼠或小鼠MOG cDNA的1.6 kb条带。使用针对完整MOG产生的特异性抗体对转染了人MOG cDNA的HeLa细胞进行免疫细胞化学分析,清楚地表明MOG作为一种内在蛋白在细胞表面表达。这些数据与预测的氨基酸序列一致,该序列包含一个信号肽和两个假定的跨膜结构域。人MOG序列的知识应有助于进一步研究其作为自身免疫性脱髓鞘疾病(如多发性硬化症)中靶抗原的潜力。

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