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Dual prenylation is required for Rab protein localization and function

机译:Rab蛋白的定位和功能需要双重异戊烯化

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摘要

The majority of Rab proteins are posttranslationally modified with two geranylgeranyl lipid moieties that enable their stable association with membranes. In this study, we present evidence to demonstrate that there is a specific lipid requirement for Rab protein localization and function. Substitution of different prenyl anchors on Rab GTPases does not lead to correct function. In the case of YPT1 and SEC4, two essential Rab genes in Saccharomyces cerevisiae, alternative lipid tails cannot support life when present as the sole source of YPT1 and SEC4. Furthermore, our data suggest that double geranyl-geranyl groups are required for Rab proteins to correctly localize to their characteristic organelle membrane. We have identified a factor, Yip1p that specifically binds the di-geranylgeranylated Rab and does not interact with mono-prenylated Rab proteins. This is the first demonstration that the double prenylation modification of Rab proteins is an important feature in the function of this small GTPase family and adds specific prenylation to the already known determinants of Rab localization. [References: 55]
机译:大多数Rab蛋白都经过两个香叶基香叶基脂质部分的翻译后修饰,使其能够与膜稳定结合。在这项研究中,我们提供证据来证明Rab蛋白的定位和功能需要特定的脂质。 Rab GTPases上不同异戊二烯基锚的替代不能导致正确的功能。对于YPT1和SEC4,这是酿酒酵母中的两个必不可少的Rab基因,当作为YPT1和SEC4的唯一来源存在时,其他脂尾不能支撑生命。此外,我们的数据表明,Rab蛋白需要两个香叶基-香叶基才能正确定位到其特征性细胞器膜上。我们已经确定了一个因子Yip1p,该因子特异性地结合了二香叶基香叶基化的Rab,并且不与单异戊二烯基化的Rab蛋白相互作用。这是第一个证明,Rab蛋白的双重异戊二烯基化修饰是这个小GTPase家族功能的重要特征,并且为已知的Rab定位决定因素增加了特定的异戊二烯基化。 [参考:55]

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