Biology Department, University of York, York YO10 5DD, U.K.
Biochem Soc Trans. 2018 Dec 17;46(6):1551-1558. doi: 10.1042/BST20180258. Epub 2018 Oct 31.
Various membrane trafficking pathways transport molecules through the endosomal system of eukaryotic cells, where trafficking decisions control the localisation and activity of a diverse repertoire of membrane protein cargoes. The budding yeast has been used to discover and define many mechanisms that regulate conserved features of endosomal trafficking. Internalised surface membrane proteins first localise to endosomes before sorting to other compartments. Ubiquitination of endosomal membrane proteins is a signal for their degradation. Ubiquitinated cargoes are recognised by the endosomal sorting complex required for transport (ESCRT) apparatus, which mediate sorting through the multivesicular body pathway to the lysosome for degradation. Proteins that are not destined for degradation can be recycled to other intracellular compartments, such as the Golgi and the plasma membrane. In this review, we discuss recent developments elucidating the mechanisms that drive membrane protein degradation and recycling pathways in yeast.
各种膜运输途径通过真核细胞的内体系统运输分子,在这个系统中,运输决策控制着多种膜蛋白货物的定位和活性。 budding yeast 已被用于发现和定义许多调节内体运输保守特征的机制。内化的表面膜蛋白首先在分选到其他隔室之前定位在内体上。内体膜蛋白的泛素化是其降解的信号。被内体分选所需的运输复合物(ESCRT)设备识别泛素化的货物,通过多泡体途径分选到溶酶体进行降解。不会降解的蛋白质可以回收再利用到其他细胞内隔室,如高尔基体和质膜。在这篇综述中,我们讨论了阐明驱动酵母中膜蛋白降解和回收途径的机制的最新进展。