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首页> 外文期刊>Journal of Biophysical and Biochemical Cytology >A family of membrane-shaping proteins at ER subdomains regulates pre-peroxisomal vesicle biogenesis
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A family of membrane-shaping proteins at ER subdomains regulates pre-peroxisomal vesicle biogenesis

机译:ER亚域的一系列膜整形蛋白质调节过氧化尿剂前体囊泡生物发生

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摘要

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.
机译:Saccharomyces Cerevisiae含有三个保守的网状蛋白和类似蛋白质的蛋白质,其通过稳定在ER小管和ER片的边缘中稳定高膜曲率来维持ER结构。缺乏所有三种蛋白质的突变体大大改变了ER形态。我们发现当PEX30P或其同源物PEX31P过表达时,在该突变体中恢复ER形状。 PEX30P可以在细胞中和重构成蛋白质胶质体时管毛膜,表明PEX30P是一种新型的ER成形蛋白。与网状龙相比,PEX30P是低丰度,我们发现它定位于ER中的子域。我们表明这些ER子域是产生大多数普利毒异素囊泡(PPV)的位点。此外,PEX30P或PEX31P的过量生产或缺失改变了PPV的大小,形状和数量。我们的研究结果表明,PEX30P和PEX31P有助于塑造并生成PPV生物发生发生的ER的区域。

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