Anterograde jelly belly and Alk receptor tyrosine kinase signaling mediates retinal axon targeting in Drosophila

被引:115
|
作者
Bazigou, Eleni
Apitz, Holger
Johansson, Jana
Loren, Christina E.
Hirst, Elizabeth M. A.
Chen, Pei-Ling
Palmer, Ruth H. [1 ]
Salecker, Iris
机构
[1] Umea Univ, Umea Ctr Mol Pathogenesis, S-90187 Umea, Sweden
[2] Natl Inst Med Res, MRC, Div Mol Neurobiol, London NW7 1AA, England
[3] Stanford Univ, Dept Neurobiol, Stanford, CA 94305 USA
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.cell.2007.02.024
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
Anaplastic lymphoma kinase (Alk) has been proposed to regulate neuronal development based on its expression pattern in vertebrates and invertebrates; however, its function in vivo is unknown. We demonstrate that Alk and its ligand Jelly belly (Jeb) play a central role as an anterograde, signaling pathway mediating neuronal circuit assembly in the Drosophila visual system. Alk is expressed and required in target neurons in the optic lobe, whereas Jeb is primarily generated by photoreceptor axons and functions in the eye to control target selection of R1-R6 axons in the lamina and R8 axons in the medulla. Impaired Jeb/Alk function affects layer-specific expression of three cell-adhesion molecules, Dumbfounded/Kirre, Roughest/IrreC, and Flamingo, in the medulla. Moreover, loss of flamingo in target neurons causes some R8-axon targeting errors observed in jeb and Alk mosaic animals. Together, these findings suggest that Jeb/Alk signaling helps R-cell axons to shape their environment for target recognition.
引用
收藏
页码:961 / 975
页数:15
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