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营养转运蛋白 Fur4 的质量控制和底物依赖性下调。

Quality control and substrate-dependent downregulation of the nutrient transporter Fur4.

机构信息

Department of Biology and Center for Cell and Genome Science, University of Utah, Salt Lake City, UT 84112-9202, USA.

出版信息

Traffic. 2013 Apr;14(4):412-27. doi: 10.1111/tra.12039. Epub 2013 Feb 4.

Abstract

Upon exposure to stress conditions, unfolded cell-surface nutrient transporters are rapidly internalized and degraded via the multivesicular body (MVB) pathway. Similarly, high concentrations of nutrients result in the downregulation of the corresponding transporters. Our studies using the yeast transporter Fur4 revealed that substrate-induced downregulation and quality control utilize a common mechanism. This mechanism is based on a conformation-sensing domain, termed LID (loop interaction domain), that regulates site-specific ubiquitination (also known as degron). Conformational alterations in the transporter induced by unfolding or substrate binding are transmitted to the LID, rendering the degron accessible for ubiquitination by Rsp5. As a consequence, the transporter is rapidly degraded. We propose that the LID-degron system is a conserved, chaperone-independent mechanism responsible for conformation-induced downregulation of many cell-surface transporters under physiological and pathological conditions.

摘要

在应激条件下,未折叠的细胞表面营养转运蛋白通过多泡体 (MVB) 途径被迅速内化和降解。同样,高浓度的营养物质会导致相应转运蛋白的下调。我们使用酵母转运蛋白 Fur4 的研究表明,底物诱导的下调和质量控制使用共同的机制。这种机制基于一种构象感应结构域,称为 LID(环相互作用结构域),它调节特定部位的泛素化(也称为降解基序)。由展开或底物结合引起的转运蛋白构象改变被传递到 LID,使降解基序可被 Rsp5 进行泛素化。结果,转运蛋白迅速降解。我们提出,LID-降解基序系统是一种保守的、独立于伴侣蛋白的机制,负责在生理和病理条件下许多细胞表面转运蛋白的构象诱导下调。

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