Axon sorting in the optic tract requires HSPG synthesis by ext2 (dackel) and extl3 (boxer)

被引:130
作者
Lee, JS
von der Hardt, S
Rusch, MA
Stringer, SE
Stickney, HL
Talbot, WS
Geisler, R
Nüsslein-Volhard, C
Selleck, SB
Chien, CB
Roehl, H
机构
[1] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT 84103 USA
[2] Max Planck Inst Entwicklungsbiol, Genet Abt, D-72076 Tubingen, Germany
[3] Univ Minnesota, Dept Pediat & Genet, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Dept Cell Biol & Dev, Minneapolis, MN 55455 USA
[5] Stanford Univ, Dept Dev Biol, Sch Med, Stanford, CA 94305 USA
[6] Univ Sheffield, Ctr Dev & Biomed Genet, Dept Biomed Sci, Sheffield S20 3TN, S Yorkshire, England
关键词
D O I
10.1016/j.neuron.2004.11.029
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Retinal ganglion cell (RGC) axons are topographically ordered in the optic tract according to their retinal origin. In zebrafish dackel (dak) and boxer (box) mutants, some dorsal RGC axons missort in the optic tract but innervate the tectum topographically. Molecular cloning reveals that dak and box encode ext2 and ext13, glycosyltransferases implicated in heparan sulfate (HS) biosynthesis. Both genes are required for HS synthesis, as shown by biochemical and immunohistochemical analysis, and are expressed maternally and then ubiquitously, likely playing permissive roles. Missorting in box can be rescued by overexpression of ext13. dak;box double mutants show synthetic pathfinding phenotypes that phenocopy robot mutants, suggesting that Robot function requires HS in vivo; however, tract sorting does not require Robo function, since it is normal in robot null mutants. This genetic evidence that heparan sulfate proteoglycan function is required for optic tract sorting provides clues to begin understanding the underlying molecular mechanisms.
引用
收藏
页码:947 / 960
页数:14
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