The exocyst is a Ral effector complex

被引:327
作者
Moskalenko, S
Henry, DO
Rosse, C
Mirey, G
Camonis, JH
White, MA
机构
[1] Univ Texas, SW Med Ctr, Dept Cell Biol, Dallas, TX 75235 USA
[2] Inst Curie, INSERM, U528, F-75248 Paris, France
关键词
D O I
10.1038/ncb728
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Delivery of cytoplasmic vesicles to discrete plasma-membrane domains is critical for establishing and maintaining cell polarity, neurite differentiation and regulated exocytosis. The exocyst is a multisubunit complex required for vectorial targeting of a subset of secretory vesicles. Mechanisms that regulate the activity of this complex in mammals are unknown. Here we show that Sec5, an integral component of the exocyst, is a direct target for activated Ral GTPases. Ral GTPases regulate targeting of basolateral proteins in epithelial cells, secretagogue-dependent exocytosis in neuroendocrine cells and assembly of exocyst complexes. These observations define Ral GTPases as critical regulators of vesicle trafficking.
引用
收藏
页码:66 / 72
页数:7
相关论文
共 44 条
[31]   The small GTPase RalA targets filamin to induce filopodia [J].
Ohta, Y ;
Suzuki, N ;
Nakamura, S ;
Hartwig, JH ;
Stossel, TP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :2122-2128
[32]   Regulation of GTP-binding state in RalA through Ca2+ and calmodulin [J].
Park, JB .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2001, 33 (01) :54-58
[33]   The mammalian Sec6/8 complex interacts with Ca2+ signaling complexes and regulates their activity [J].
Shin, DM ;
Zhao, XS ;
Zeng, WZ ;
Mozhayeva, M ;
Muallem, S .
JOURNAL OF CELL BIOLOGY, 2000, 150 (05) :1101-1112
[34]   Synaptogyrins regulate Ca2+-dependent exocytosis in PC12 cells [J].
Sugita, S ;
Janz, R ;
Südhof, TC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (27) :18893-18901
[35]   α-latrotoxin receptor CIRL/latrophilin 1 (CL1) defines an unusual family of ubiquitous G-protein-linked receptors -: G-protein coupling not required for triggering exocytosis [J].
Sugita, S ;
Ichtchenko, K ;
Khvotchev, M ;
Südhof, TC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (49) :32715-32724
[36]   Biochemical characterization of C3G: an exchange factor that discriminates between Rap1 and Rap2 and is not inhibited by Rap1A(S17N) [J].
vandenBerghe, N ;
Cool, RH ;
Horn, G ;
Wittinghofer, A .
ONCOGENE, 1997, 15 (07) :845-850
[37]  
VOJTEK AB, 1995, METHOD ENZYMOL, V255, P331
[38]   ASSOCIATION OF 3 SMALL GTP-BINDING PROTEINS WITH CHOLINERGIC SYNAPTIC VESICLES [J].
VOLKNANDT, W ;
PEVSNER, J ;
ELFERINK, LA ;
SCHELLER, RH .
FEBS LETTERS, 1993, 317 (1-2) :53-56
[39]   MUTATIONAL ANALYSIS OF SEC4 SUGGESTS A CYCLICAL MECHANISM FOR THE REGULATION OF VESICULAR TRAFFIC [J].
WALWORTH, NC ;
GOUD, B ;
KABCENELL, AK ;
NOVICK, PJ .
EMBO JOURNAL, 1989, 8 (06) :1685-1693
[40]   HYDROLYSIS OF GTP BY SEC4 PROTEIN PLAYS AN IMPORTANT ROLE IN VESICULAR TRANSPORT AND IS STIMULATED BY A GTPASE-ACTIVATING PROTEIN IN SACCHAROMYCES-CEREVISIAE [J].
WALWORTH, NC ;
BRENNWALD, P ;
KABCENELL, AK ;
GARRETT, M ;
NOVICK, P .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (05) :2017-2028