Trio combines with Dock to regulate Pak activity during photoreceptor axon pathfinding in Drosophila

被引:253
作者
Newsome, TP
Schmidt, S
Dietzl, G
Keleman, K
Åsling, B
Debant, A
Dickson, BJ
机构
[1] Res Inst Mol Pathol, A-1030 Vienna, Austria
[2] Ctr Rech Biochim Macromol, CNRS, UPR1086, F-34293 Montpellier 5, France
关键词
D O I
10.1016/S0092-8674(00)80838-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Correct pathfinding by Drosophila photoreceptor axons requires recruitment of p21-activated kinase (Pak) to the membrane by the SH2-SH3 adaptor Dock. Here, we identify the guanine nucleotide exchange factor (GEF) Trio as another essential component in photoreceptor axon guidance. Regulated exchange activity of one of the two Trio GEF domains is critical for accurate pathfinding. This GEF domain activates Rac, which in turn activates Pak. Mutations in trio result in projection defects similar to those observed in both Pak and dock mutants, and trio interacts genetically with Rac, Pak, and dock. These data define a signaling pathway from Trio to Rac to Pak that links guidance receptors to the growth cone cytoskeleton. We propose that distinct signals transduced via Trio and Dock act combinatorially to activate Pak in spatially restricted domains within the growth cone, thereby controlling the direction of axon extension.
引用
收藏
页码:283 / 294
页数:12
相关论文
共 52 条
[21]   Pak functions downstream of dock to regulate photoreceptor axon guidance in Drosophila [J].
Hing, H ;
Xiao, J ;
Harden, N ;
Lim, L ;
Zipursky, SL .
CELL, 1999, 97 (07) :853-863
[22]   INHIBITION OF LYSOPHOSPHATIDATE-INDUCED AND THROMBIN-INDUCED NEURITE RETRACTION AND NEURONAL CELL ROUNDING BY ADP-RIBOSYLATION OF THE SMALL GTP-BINDING PROTEIN-RHO [J].
JALINK, K ;
VANCORVEN, EJ ;
HENGEVELD, T ;
MORII, N ;
NARUMIYA, S ;
MOOLENAAR, WH .
JOURNAL OF CELL BIOLOGY, 1994, 126 (03) :801-810
[23]   Localization of the G protein βγ complex in living cells during chemotaxis [J].
Jin, T ;
Zhang, N ;
Long, Y ;
Parent, CA ;
Devreotes, PN .
SCIENCE, 2000, 287 (5455) :1034-1036
[24]  
Jin Z, 1997, J NEUROSCI, V17, P6256
[25]   LOSS OF THE AMINO-TERMINAL HELIX-LOOP-HELIX DOMAIN OF THE VAV PROTOONCOGENE ACTIVATES ITS TRANSFORMING POTENTIAL [J].
KATZAV, S ;
CLEVELAND, JL ;
HESLOP, HE ;
PULIDO, D .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (04) :1912-1920
[26]  
Kaufmann N, 1998, DEVELOPMENT, V125, P453
[27]   Rho family GTPases and neuronal growth cone remodelling: Relationship between increased complexity induced by Cdc42Hs, Rac1, and acetylcholine and collapse induced by RhoA and lysophosphatidic acid [J].
Kozma, R ;
Sarner, S ;
Ahmed, S ;
Lim, L .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (03) :1201-1211
[28]   CONDITIONS FOR THE PRIMARY CULTURE OF EYE IMAGINAL DISCS FROM DROSOPHILA-MELANOGASTER [J].
LI, CL ;
MEINERTZHAGEN, IA .
JOURNAL OF NEUROBIOLOGY, 1995, 28 (03) :363-380
[29]   Dosage-sensitive, reciprocal genetic interactions between the Abl tyrosine kinase and the putative GEF trio reveal trio's role in axon pathfinding [J].
Liebl, EC ;
Forsthoefel, DJ ;
Franco, LS ;
Sample, SH ;
Hess, JE ;
Cowger, JA ;
Chandler, MP ;
Shupert, AM ;
Seeger, MA .
NEURON, 2000, 26 (01) :107-118
[30]   NMR structure and mutagenesis of the N-terminal Dbl homology domain of the nucleotide exchange factor trio [J].
Liu, XH ;
Wang, H ;
Eberstadt, M ;
Schnuchel, A ;
Olejniczak, ET ;
Meadows, RP ;
Schkeryantz, JM ;
Janowick, DA ;
Harlan, JE ;
Harris, EAS ;
Staunton, DE ;
Fesik, SW .
CELL, 1998, 95 (02) :269-277