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人Rab GDI脑型同工型的克隆及其在人神经母细胞瘤细胞系和肿瘤标本中的表达。

Cloning of a brain-type isoform of human Rab GDI and its expression in human neuroblastoma cell lines and tumor specimens.

作者信息

Nishimura N, Goji J, Nakamura H, Orita S, Takai Y, Sano K

机构信息

Department of Pediatrics, Kobe University School of Medicine, Japan.

出版信息

Cancer Res. 1995 Nov 15;55(22):5445-50.

PMID:7585614
Abstract

Rab proteins, a family of Ras-related small GTP-binding proteins, play a key role in regulating intracellular vesicle trafficking. Rab GDP dissociation inhibitor (GDI3) forms a soluble complex with Rab proteins and thereby prevents the exchange of GDP for GTP. Recently, two isoforms of Rab GDI cDNA were isolated from rats and mice. In this study, we have isolated a brain-type isoform of human Rab GDI cDNA and examined its expression in neuroblastoma. We tentatively designate it as human Rab GDI alpha (hu GDI alpha) and another human Rab GDI, as human Rab GDI beta (hu GDI beta). Hu GDI alpha cDNA encodes a protein of 447 amino acids with a deduced molecular weight of 50,200. Northern blot analysis revealed that hu GDI alpha gene is expressed abundantly in the brain but much less in other tissues, while hu GDI beta gene is ubiquitously expressed. All human neuroblastoma cell lines and tumor specimens examined express hu GDI alpha gene to various extents, while a human T cell leukemia cell line, MOLT3, does not. The levels of both hu GDI alpha and beta mRNA were constant in a human neuroblastoma cell line, NB1, during its neuronal differentiation, while Rab3A and neurofilament-L gene expression and the number of neurosecretory granules were elevated at this condition. These results suggest that hu GDI alpha gene expression is not related to the differentiation state of neuronal cells.

摘要

Rab蛋白是Ras相关的小GTP结合蛋白家族,在调节细胞内囊泡运输中起关键作用。Rab GDP解离抑制剂(GDI3)与Rab蛋白形成可溶性复合物,从而阻止GDP与GTP的交换。最近,从大鼠和小鼠中分离出了Rab GDI cDNA的两种亚型。在本研究中,我们分离出了人Rab GDI cDNA的脑型亚型,并检测了其在神经母细胞瘤中的表达。我们暂时将其命名为人Rab GDIα(hu GDIα),另一种人Rab GDI命名为人Rab GDIβ(hu GDIβ)。Hu GDIα cDNA编码一种由447个氨基酸组成的蛋白质,推导分子量为50200。Northern印迹分析显示,hu GDIα基因在脑中大量表达,但在其他组织中表达较少,而hu GDIβ基因则广泛表达。所有检测的人神经母细胞瘤细胞系和肿瘤标本均不同程度地表达hu GDIα基因,而人T细胞白血病细胞系MOLT3则不表达。在人神经母细胞瘤细胞系NB1的神经元分化过程中,hu GDIα和β mRNA的水平保持恒定,而在此条件下Rab3A和神经丝-L基因的表达以及神经分泌颗粒的数量增加。这些结果表明,hu GDIα基因的表达与神经元细胞的分化状态无关。

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