S-Palmitoylation Sorts Membrane Cargo for Anterograde Transport in the Golgi

被引:103
作者
Ernst, Andreas M. [1 ]
Syed, Saad A. [1 ]
Zaki, Omar [1 ]
Bottanelli, Francesca [1 ]
Zheng, Hong [1 ]
Hacke, Moritz [1 ]
Xi, Zhiqun [1 ]
Rivera-Molina, Felix [1 ]
Graham, Morven [1 ]
Rebane, Aleksander A. [1 ]
Bjorkholm, Patrik [1 ]
Baddeley, David [1 ]
Toomre, Derek [1 ]
Pincet, Frederic [1 ,2 ]
Rothman, James E. [1 ]
机构
[1] Yale Sch Med, Dept Cell Biol, New Haven, CT 06520 USA
[2] UPMC Univ, Sorbonne Univ, Univ Paris Diderot,Lab Phys Stat,CNRS, PSL Res Univ,Ecole Normale Super,Sorbonne Paris C, Paris, France
关键词
CYSTEINE-RICH DOMAIN; STOMATITIS-VIRUS GLYCOPROTEIN; ACYL-COENZYME-A; PROTEIN PALMITOYLATION; PLASMA-MEMBRANE; IDENTIFICATION; VESICLES; PALMITOYLTRANSFERASE; INHIBITORS; MECHANISM;
D O I
10.1016/j.devcel.2018.10.024
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
While retrograde cargo selection in the Golgi is known to depend on specific signals, it is unknown whether anterograde cargo is sorted, and antero-grade signals have not been identified. We suggest here that S-palmitoylation of anterograde cargo at the Golgi membrane interface is an anterograde signal and that it results in concentration in curved regions at the Golgi rims by simple physical chemistry. The rate of transport across the Golgi of two S-palmitoylated membrane proteins is controlled by 5-palmitoylation. The bulk of 5-palmitoylated pro-teins in the Golgi behave analogously, as revealed by click chemistry-based fluorescence and electron microscopy. These palmitoylated cargos concen-trate in the most highly curved regions of the Golgi membranes, including the fenestrated perimeters of cisternae and associated vesicles. A palmitoylated transmembrane domain behaves similarly in model systems.
引用
收藏
页码:479 / +
页数:22
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