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哺乳动物KDEL受体p23的分子克隆、特性分析、亚细胞定位及动态变化

Molecular cloning, characterization, subcellular localization and dynamics of p23, the mammalian KDEL receptor.

作者信息

Tang B L, Wong S H, Qi X L, Low S H, Hong W

机构信息

Membrane Biology Laboratory, National University of Singapore.

出版信息

J Cell Biol. 1993 Jan;120(2):325-38. doi: 10.1083/jcb.120.2.325.

Abstract

We have isolated a cDNA clone (mERD2) for the mammalian (bovine) homologue of the yeast ERD2 gene, which codes for the yeast HDEL receptor. The deduced amino acid sequence bears extensive homology to its yeast counterpart and is almost identical to a previously described human sequence. The sequence predicts a very hydrophobic protein with multiple membrane spanning domains, as confirmed by analysis of the in vitro translation product. The protein encoded by mERD2 (p23) has widespread occurrence, being present in all the cell types examined. p23 was localized to the cis-side of the Golgi apparatus and to a spotty intermediate compartment which mediates ER to Golgi transport. A majority of the intracellular staining could be accumulated in the intermediate compartment by a low temperature (15 degrees C) or brefeldin A. During recovery from these treatments, the spotty intermediate compartment staining of p23 was shifted to the perinuclear staining of the Golgi apparatus and tubular structures marked by p23 were observed. These tubular structures may serve to mediate transport between the intermediate compartment and the Golgi apparatus.

摘要

我们已经分离出了一个cDNA克隆(mERD2),它是酵母ERD2基因的哺乳动物(牛)同源物,该基因编码酵母HDEL受体。推导的氨基酸序列与其酵母对应物具有广泛的同源性,并且与先前描述的人类序列几乎相同。该序列预测了一种具有多个跨膜结构域的高度疏水蛋白,体外翻译产物的分析证实了这一点。mERD2编码的蛋白(p23)广泛存在于所有检测的细胞类型中。p23定位于高尔基体的顺面以及介导内质网到高尔基体运输的斑点状中间区室。大部分细胞内染色可通过低温(15摄氏度)或布雷菲德菌素A积累在中间区室中。在从这些处理中恢复期间,p23的斑点状中间区室染色转移到高尔基体的核周染色,并观察到由p23标记的管状结构。这些管状结构可能有助于介导中间区室与高尔基体之间的运输。

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