C-elegans slit acts in midline, dorsal-ventral, and anterior-posterior guidance via the SAX-3/Robo receptor

被引:182
作者
Hao, JC
Yu, TW
Fujisawa, K
Culotti, JG
Gengyo-Ando, K
Mitani, S
Moulder, G
Barstead, R
Tessier-Lavigne, M
Bargmann, CI [1 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Anat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, Program Neurosci, San Francisco, CA 94143 USA
[3] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[4] Tokyo Womens Med Univ, Sch Med, Dept Physiol, Tokyo 1628666, Japan
[5] Japan Sci & Technol Corp, PRESTO, Tokyo 1628666, Japan
[6] Oklahoma Med Res Fdn, Oklahoma City, OK 73104 USA
关键词
D O I
10.1016/S0896-6273(01)00448-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Robo receptors interact with ligands of the Slit family. The nematode C. elegans has one Robo receptor (SAX-3) and one Slit protein (SLT-1), which direct ventral axon guidance and guidance at the midline. In larvae, slt-1 expression in dorsal muscles repels axons to promote ventral guidance. SLT-1 acts through the SAX-3 receptor, in parallel with the ventral attractant UNC-6 (Netrin). Removing both UNC-6 and SLT-1 eliminates all ventral guidance information for some axons, revealing an underlying longitudinal guidance pathway. In the embryo, slt-1 is expressed at high levels in anterior epidermis. Embryonic expression of SLT-1 provides anterior-posterior guidance information to migrating CAN neurons. Surprisingly, slt-1 mutants do not exhibit the nerve ring and epithelial defects of sax-3 mutants, suggesting that SAX-3 has both Slit-dependent and Slit-independent functions in development.
引用
收藏
页码:25 / 38
页数:14
相关论文
共 50 条
[1]  
Ba-Charvet KTN, 2001, J NEUROSCI, V21, P4281
[2]   Slit2-mediated chemorepulsion and collapse of developing forebrain axons [J].
Ba-Charvet, KTN ;
Brose, K ;
Marillat, V ;
Kidd, T ;
Goodman, CS ;
Tessier-Lavigne, M ;
Sotelo, C ;
Chédotal, A .
NEURON, 1999, 22 (03) :463-473
[3]   Repellent signaling by slit requires the leucine-rich repeats [J].
Battye, R ;
Stevens, A ;
Perry, RL ;
Jacobs, JR .
JOURNAL OF NEUROSCIENCE, 2001, 21 (12) :4290-4298
[4]  
BRENNER S, 1974, GENETICS, V77, P71
[5]   Slit proteins bind robe receptors and have an evolutionarily conserved role in repulsive axon guidance [J].
Brose, K ;
Bland, KS ;
Wang, KH ;
Arnott, D ;
Henzel, W ;
Goodman, CS ;
Tessier-Lavigne, M ;
Kidd, T .
CELL, 1999, 96 (06) :795-806
[6]   UNC-40, a C-elegans homolog of DCC (Deleted in Colorectal Cancer), is required in motile cells responding to UNC-6 netrin cues [J].
Chan, SSY ;
Zheng, H ;
Su, MW ;
Wilk, R ;
Killeen, MT ;
Hedgecock, EM ;
Culotti, JG .
CELL, 1996, 87 (02) :187-195
[7]   The ephrin VAB-2/EFN-1 functions in neuronal signaling to regulate epidermal morphogenesis in C-elegans [J].
Chin-Sang, ID ;
George, SE ;
Ding, M ;
Moseley, SL ;
Lynch, AS ;
Chisholm, AD .
CELL, 1999, 99 (07) :781-790
[8]   Meiotic recombination in C-elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis [J].
Dernburg, AF ;
McDonald, K ;
Moulder, G ;
Barstead, R ;
Dresser, M ;
Villeneuve, AM .
CELL, 1998, 94 (03) :387-398
[9]  
Durbin RM, 1987, THESIS U CAMBRIDGE C
[10]  
Erskine L, 2000, J NEUROSCI, V20, P4975