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dp115在果蝇tER位点组织中的新作用。

A novel role for dp115 in the organization of tER sites in Drosophila.

作者信息

Kondylis Vangelis, Rabouille Catherine

机构信息

The Wellcome Trust Center for Cell Biology, Institute for Cell and Molecular Biology, University of Edinburgh, UK.

出版信息

J Cell Biol. 2003 Jul 21;162(2):185-98. doi: 10.1083/jcb.200301136.

Abstract

Here, we describe that depletion of the Drosophila homologue of p115 (dp115) by RNA interference in Drosophila S2 cells led to important morphological changes in the Golgi stack morphology and the transitional ER (tER) organization. Using conventional and immunoelectron microscopy and confocal immunofluorescence microscopy, we show that Golgi stacks were converted into clusters of vesicles and tubules, and that the tERs (marked by Sec23p) lost their focused organization and were now dispersed throughout the cytoplasm. However, we found that this morphologically altered exocytic pathway was nevertheless largely competent in anterograde protein transport using two different assays. The effects were specific for dp115. Depletion of the Drosophila homologues of GM130 and syntaxin 5 (dSed5p) did not lead to an effect on the tER organization, though the Golgi stacks were greatly vesiculated in the cells depleted of dSed5p. Taken together, these studies suggest that dp115 could be implicated in the architecture of both the Golgi stacks and the tER sites.

摘要

在此,我们描述了通过RNA干扰在果蝇S2细胞中耗尽p115的果蝇同源物(dp115)导致高尔基体堆栈形态和过渡性内质网(tER)组织发生重要的形态学变化。使用传统电子显微镜、免疫电子显微镜和共聚焦免疫荧光显微镜,我们发现高尔基体堆栈转变为囊泡和小管簇,并且tER(由Sec23p标记)失去了其集中的组织结构,现在分散在整个细胞质中。然而,我们发现,使用两种不同的检测方法,这种形态改变的外排途径在很大程度上仍能进行顺向蛋白质转运。这些效应是dp115特有的。耗尽GM130和Syntaxin 5的果蝇同源物(dSed5p)对tER组织没有影响,尽管在耗尽dSed5p的细胞中高尔基体堆栈大量囊泡化。综上所述,这些研究表明dp115可能与高尔基体堆栈和tER位点的结构有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c27/2172793/f9c24dbcf898/200301136f1.jpg

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