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内质网亚结构域处的一族膜塑形蛋白调节过氧化物酶体前体小泡的生物发生。

A family of membrane-shaping proteins at ER subdomains regulates pre-peroxisomal vesicle biogenesis.

作者信息

Joshi Amit S, Huang Xiaofang, Choudhary Vineet, Levine Tim P, Hu Junjie, Prinz William A

机构信息

Laboratory of Cell and Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892.

Department of Genetics and Cell Biology, College of Life Sciences, Nankai University, Tianjin 300071, China.

出版信息

J Cell Biol. 2016 Nov 21;215(4):515-529. doi: 10.1083/jcb.201602064. Epub 2016 Nov 8.

Abstract

Saccharomyces cerevisiae contains three conserved reticulon and reticulon-like proteins that help maintain ER structure by stabilizing high membrane curvature in ER tubules and the edges of ER sheets. A mutant lacking all three proteins has dramatically altered ER morphology. We found that ER shape is restored in this mutant when Pex30p or its homologue Pex31p is overexpressed. Pex30p can tubulate membranes both in cells and when reconstituted into proteoliposomes, indicating that Pex30p is a novel ER-shaping protein. In contrast to the reticulons, Pex30p is low abundance, and we found that it localizes to subdomains in the ER. We show that these ER subdomains are the sites where most preperoxisomal vesicles (PPVs) are generated. In addition, overproduction or deletion of Pex30p or Pex31p alters the size, shape, and number of PPVs. Our findings suggest that Pex30p and Pex31p help shape and generate regions of the ER where PPV biogenesis occurs.

摘要

酿酒酵母含有三种保守的网质蛋白和类网质蛋白,它们通过稳定内质网(ER)小管以及内质网片层边缘的高膜曲率来帮助维持内质网结构。缺乏所有这三种蛋白的突变体具有显著改变的内质网形态。我们发现,当过表达Pex30p或其同源物Pex31p时,该突变体的内质网形状得以恢复。Pex30p在细胞内以及重组到蛋白脂质体中时都能使膜形成小管,这表明Pex30p是一种新型的内质网塑形蛋白。与网质蛋白不同,Pex30p丰度较低,并且我们发现它定位于内质网的亚结构域。我们表明,这些内质网亚结构域是大多数过氧化物酶体前体小泡(PPV)产生的部位。此外,Pex30p或Pex31p的过量表达或缺失会改变PPV的大小、形状和数量。我们的研究结果表明,Pex30p和Pex31p有助于塑造并产生内质网中发生PPV生物发生的区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/248b/5119935/50004cc04a6b/JCB_201602064_Fig1.jpg

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