Retinal axon target selection in Drosophila is regulated by a receptor protein tyrosine phosphatase

被引:130
作者
Garrity, PA
Lee, CH
Salecker, I
Robertson, HC
Desai, CJ
Zinn, K
Zipursky, SL [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Inst Mol Biol, Dept Biol Chem,Howard Hughes Med Inst, Los Angeles, CA 90095 USA
[2] MIT, Dept Biol, Cambridge, MA 02138 USA
[3] Vanderbilt Univ, Med Ctr, Ctr Molec Neurosci, Nashville, TN 37232 USA
[4] CALTECH, Div Biol, Pasadena, CA 91125 USA
关键词
D O I
10.1016/S0896-6273(00)80730-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Different Drosophila photoreceptors (R cells) connect to neurons in different optic lobe layers. R1-R6 axons project to the lamina; R7 and R8 axons project to separate layers of the medulla. We show a receptor tyrosine phosphatase, PTP69D, is required for lamina target specificity. In Ptp69D mutants, R1-R6 project through the lamina, terminating in the medulla. Genetic mosaics, transgene rescue, and immunolocalization indicate PTP69D functions in R1-R6 growth cones. PTP69D overexpression in R7 and R8 does not respecify their connections, suggesting PTP69D acts in combination with other factors to determine target specificity. Structure-function analysis indicates the extracellular fibronectin type III domains and intracellular phosphatase activity are required for targeting. We propose PTP69D promotes R1-R6 targeting in response to extracellular signals by dephosphorylating substrate(s) in R1-R6 growth cones.
引用
收藏
页码:707 / 717
页数:11
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