Coordination of Golgi functions by phosphatidylinositol 4-kinases

被引:144
作者
Graham, Todd R. [1 ]
Burd, Christopher G. [2 ]
机构
[1] Vanderbilt Univ, Dept Biol Sci, Nashville, TN 37235 USA
[2] Univ Penn, Dept Cell & Dev Biol, Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
OXYSTEROL-BINDING-PROTEIN; D-MEDIATED PHOSPHORYLATION; PLASMA-MEMBRANE TRANSPORT; NEURONAL CALCIUM SENSOR-1; P-TYPE ATPASE; ENDOPLASMIC-RETICULUM; SECRETORY VESICLES; GLYCOSPHINGOLIPID SYNTHESIS; TRANSLOCASE ACTIVITY; STEROL TRANSPORT;
D O I
10.1016/j.tcb.2010.10.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Phosphatidylinositol 4-kinases (PI4Ks) regulate vesicle-mediated export from the Golgi apparatus via phosphatidylinositol 4-phosphate (PtdIns4P) binding effector proteins that control vesicle budding reactions and regulate membrane dynamics. Evidence has emerged from the characterization of Golgi PI4K effectors that vesicle budding and lipid dynamics are tightly coupled via a regulatory network that ensures that the appropriate membrane composition is established before a transport vesicle buds horn the Golgi. An important hub of this network is protein kinase D, which regulates the activity of PI4K and several PtdIns4P effectors that control sphingolipid and sterol content of Golgi membranes. Other newly identified PtdIns4P effectors include Vps74/GOLPH3, a phospholipid flippase called Drs2 and Sec2, a Rab guanine nucleotide exchange factor (GEF). These effectors orchestrate membrane transformation events facilitating vesicle formation and targeting. In this review, we discuss how PtdIns4P signaling is integrated with membrane biosynthetic and vesicle budding machineries to potentially coordinate these crucial functions of the Golgi apparatus.
引用
收藏
页码:113 / 121
页数:9
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