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哺乳动物COPII包被的内质网出口位点的从头形成、融合和裂变。

De novo formation, fusion and fission of mammalian COPII-coated endoplasmic reticulum exit sites.

作者信息

Stephens David J

机构信息

Department of Biochemistry, University of Bristol, School of Medical Sciences, University Walk, Bristol BS8 1TD, UK.

出版信息

EMBO Rep. 2003 Feb;4(2):210-7. doi: 10.1038/sj.embor.embor736.

Abstract

Transport between the endoplasmic reticulum (ER) and Golgi is mediated by the sequential action of the COPII and COPI coat complexes. COPII subunits are recruited to the ER membrane where they mediate the selection of cargo for transport to the Golgi, and also membrane deformation and vesicle formation. New ER exit sites can be generated by lateral growth and medial fission (in Pythium sp.) or by de novo formation (in Pichia pastoris) but it is not known how mammalian ER exit sites form. Here, time-lapse imaging of COPII-coated structures in live mammalian cells reveals that the number of ER export sites increases greatly during interphase by de novo formation. These results show the fusion of pre-existing ER export sites and the fission of larger structures. These three mechanisms of de novo formation, fusion and fission probably cooperate to regulate the size of these sites in mammalian cells.

摘要

内质网(ER)与高尔基体之间的运输是由COPII和COPI衣被复合体的顺序作用介导的。COPII亚基被招募到内质网膜上,在那里它们介导选择运往高尔基体的货物,还介导膜变形和囊泡形成。新的内质网出口位点可通过侧向生长和中间裂变(在腐霉菌属中)或从头形成(在巴斯德毕赤酵母中)产生,但尚不清楚哺乳动物内质网出口位点是如何形成的。在这里,对活的哺乳动物细胞中COPII包被结构的延时成像显示,内质网输出位点的数量在间期通过从头形成而大幅增加。这些结果显示了先前存在的内质网输出位点的融合以及较大结构的裂变。从头形成、融合和裂变这三种机制可能协同作用来调节哺乳动物细胞中这些位点的大小。

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