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A lipid-mediated quality control process in the Golgi apparatus in yeast

机译:酵母中高尔基体中脂质介导的质量控制过程

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When heme biosynthesis is disrupted, the yeast Saccharomyces cerevisiae becomes unable to synthesize its major sterol, ergosterol, and desaturate fatty acids. We took advantage of this physiological peculiarity to evaluate the consequences of ergosterol and/or unsaturated fatty acid (UFA) depletions on the biogenesis of a model polytopic plasma membrane protein, the uracil permease Fur4p. We show that under UFA shortage, which results in low amounts of diunsaturated phospholipid species, and under ergosterol depletion, Fur4p is prematurely routed from the Golgi apparatus to the vacuolar lumen in a process that requires the ubiquitin ligase Rsp5p. Interestingly, this diversion is not correlated to Fur4p exclusion from detergent-resistant membranes. In an independent set of experiments, we show that Fur4p targeting to the plasma membrane depends on phosphatidylethanolamine amounts and more specifically on the propensity of this phospholipid to form a hexagonal phase. In light of recent literature, we propose a model in which ergosterol and diunsaturated phospholipid species maintain optimal membrane curvature for Fur4p to evade the Golgi quality control process and to be properly delivered to its normal destination.
机译:当血红素的生物合成被破坏时,酵母酿酒酵母变得无法合成其主要固醇,麦角固醇和去饱和脂肪酸。我们利用这种生理特性来评估麦角固醇和/或不饱和脂肪酸(UFA)消耗对模型多位质膜蛋白尿嘧啶通透酶Fur4p的生物合成的影响。我们显示,在UFA短缺的情况下,这会导致少量的双不饱和磷脂种类减少,而在麦角固醇耗竭的情况下,Fur4p在需要泛素连接酶Rsp5p的过程中过早地从高尔基体转运至液泡腔。有趣的是,这种转移与从抗洗涤剂膜中排除Fur4p无关。在一组独立的实验中,我们显示了靶向细胞质膜的Fur4p取决于磷脂酰乙醇胺的量,更具体地取决于该磷脂形成六方相的倾向。根据最近的文献,我们提出了一种模型,其中麦角固醇和二不饱和磷脂物质保持Fur4p的最佳膜曲率,从而逃避了高尔基体质控制过程,并正确地传递到其正常目的地。

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