Control of dendritic branching and tiling by the tricornered-kinase/furry signaling pathway in Drosophila sensory neurons

被引:187
作者
Emoto, K
He, Y
Ye, B
Grueber, WB
Adler, PN
Jan, LY
Jan, YN
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Physiol & Biochem, San Francisco, CA 94143 USA
[2] Univ Virginia, Dept Biol, Charlottesville, VA 22903 USA
[3] Univ Virginia, Ctr Canc, Charlottesville, VA 22903 USA
关键词
D O I
10.1016/j.cell.2004.09.036
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
To cover the receptive field completely but without redundancy, neurons of certain functional groups exhibit tiling of their dendrites via dendritic repulsion. Here we show that two evolutionarily conserved proteins, the Tricornered (Trc) kinase and Furry (Fry), are essential for tiling and branching control of Drosophila sensory neuron dendrites. Dendrites of fry and trc mutants display excessive terminal branching and fail to avoid homologous dendritic branches, resulting in significant overlap of the dendritic fields. Trc control of dendritic branching involves regulation of RacGTPase, a pathway distinct from the action of Trc in tiling. Time-lapse analysis further reveals a specific loss of the ability of growing dendrites to turn away from nearby dendritic branches in fry mutants, suggestive of a defect in like-repels-like avoidance. Thus, the Trc/ Fry signaling pathway plays a key role in patterning dendritic fields by promoting avoidance between homologous dendrites as well as by limiting dendritic branching.
引用
收藏
页码:245 / 256
页数:12
相关论文
共 51 条
[1]   Planar signaling and morphogenesis in Drosophila [J].
Adler, PN .
DEVELOPMENTAL CELL, 2002, 2 (05) :525-535
[2]   MORPHOLOGICAL-DIFFERENTIATION OF THE EMBRYONIC PERIPHERAL NEURONS IN DROSOPHILA [J].
BODMER, R ;
JAN, YN .
ROUXS ARCHIVES OF DEVELOPMENTAL BIOLOGY, 1987, 196 (02) :69-77
[3]   Sequoia, a tramtrack-related zinc finger protein, functions as a pan-neural regulator for dendrite and axon morphogenesis in Drosophila [J].
Brenman, JE ;
Gao, FB ;
Jan, LY ;
Jan, YN .
DEVELOPMENTAL CELL, 2001, 1 (05) :667-677
[4]   Dendritic arbor development and synaptogenesis [J].
Cline, HT .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (01) :118-126
[5]   Yeast Cbk1 and Mob2 activate daughter-specific genetic programs to induce asymmetric cell fates [J].
Colman-Lerner, A ;
Chin, TE ;
Brent, R .
CELL, 2001, 107 (06) :739-750
[6]  
Cong JL, 2001, DEVELOPMENT, V128, P2793
[7]   Mosaic arrangement of ganglion cell receptive fields in rabbit retina [J].
DeVries, SH ;
Baylor, DA .
JOURNAL OF NEUROPHYSIOLOGY, 1997, 78 (04) :2048-2060
[8]   Human mob proteins regulate the NDR1 and NDR2 serine-threonine kinases [J].
Devroe, E ;
Erdjument-Bromage, H ;
Tempst, P ;
Silver, PA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (23) :24444-24451
[9]   Pag1p, a novel protein associated with protein kinase cbk1p, is required for cell morphogenesis and proliferation in Saccharomyces cerevisiae [J].
Du, LL ;
Novick, P .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (02) :503-514
[10]   Mechanosensory neurite termination and tiling depend on SAX-2 and the SAX-1 kinase [J].
Gallegos, ME ;
Bargmann, CI .
NEURON, 2004, 44 (02) :239-249