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Guigage axonal dans le système nerveux ventral chez

Jean-Maurice Dura Institut de Génétique Humaine jmdura@igh.cnrs.fr. Guigage axonal dans le système nerveux ventral chez Drosophila : r ôles du récepteur DRL et de son ligand WNT5. Callahan et al., Nature 1995 Bonkowsky et al., Nature 1999 Yoshikawa et al., Nature 2003.

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Guigage axonal dans le système nerveux ventral chez

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  1. Jean-Maurice Dura Institut de Génétique Humaine jmdura@igh.cnrs.fr Guigage axonal dans le système nerveux ventral chez Drosophila: rôles du récepteur DRL et de son ligand WNT5 Callahan et al., Nature 1995 Bonkowsky et al., Nature 1999 Yoshikawa et al., Nature 2003

  2. Strong similarities between Drosophila and human • More than 50% of the 15.000 Drosophila genes have a strong similarity with a human gene. • Amongst 289 human genes involved in a severe pathology, 177 have a clear homologue in Drosophila. • Numerous molecular pathway are very well conserved (signal transduction; neurotransmitters; etc......).

  3. Crible “enhancer trap” avec P[etau-lacZ] qui permet de bien visualiser les trajets axonaux - crible de 2400 nouvelles insertions au hasard.

  4. +/+ anti-HRP drlP[etau-lacZ]/+ anti-gal 20 interneurons / hemisegment 200 interneurons / hemisegment

  5. drlP : insertion - allèle perte de fonction - lacZ exprimé comme drl+ drlPexc : excision précise - allèle sauvage drlR : délétion - allèle null

  6. drlP/+ drlP/+ [+] [+] drlP/drlP drlP/drlR [-] [-] defasciculation 10% cross in PC

  7. drlP/drlPexc drlR/drlR [+] [-] anti-Fas2 anti-DRL @ 10h anti-DRL @ 11.5h

  8. The DRL protein

  9. 30% cross in PC

  10. drlP : insertion - allèle perte de fonction - lacZ exprimé comme drl+ drlPexc : excision précise - allèle sauvage drlR : délétion - allèle null drlRed2 : allèle null - lacZ exprimé comme drl+

  11. in yeast GAL4 881 aa: regulator of transcription of genes induced by galactose (GAL10 and GAL1) by directly binding to 4 related 17 bp sites defining an Upstream Activating Sequences (UAS) in Drosophila (transgenesis via P transposable element) (no deleterious effect)

  12. eagle-GAL4 +UAS-tau-lacZ +UAS-drl +UAS-drlE: cross in AC + PC cross only in AC cross in AC + PC

  13. drl instructs crossing axons to choose AC: - attractive to AC? - repulsive to PC?

  14. ap-GAL4/UAS-tau-lacZ ap-GAL4/UAS-tau-lacZ; 2xUAS-drl drlrecognizes a repulsive cue in the PC

  15. ap-GAL4/UAS-tau-lacZ + UAS-drl : no crossing - no effect + UAS-comm : crossing in AC +PC + UAS-comm + UAS-drl : crossing only in AC + UAS-comm + UAS-drlE : crossing in AC +PC

  16. The DRL protein

  17. DRL-myc soluble extracellular domain probe: should correspond to putative DRL ligand red: DRL-myc green: endogenous drl expression

  18. Looking for the ligand

  19. genetic screen for DRL ligand: suppression of drl gain-of-function 80% genome deficiencies screen eg-GAL4 UAS-drl; def/+ 250 defs one by one One particular def is selected, then overlaping defs, and finally producing mutant of interesting gene

  20. Wnt5 transcripts are localized in the PC

  21. WNT5 protein is localized in the PC and in the AC

  22. DRL-myc soluble extracellular domain probe: should correspond to putative DRL ligand red: DRL-myc green: endogenous drl expression myc

  23. Embryos stained with BP102 (all axons)

  24. embryos stained for subsets of AC axons: +/Y; drlP/+ +/Y; drlP/drlRWnt5D7/Y; drlP/+

  25. embryos stained for all axons: anti-HRP midline glia GAL4/UAS-Wnt5; drl+/drl+ drl-/drl- embryos stained for subsets of PC axons: Wnt5 mutants are normal

  26. DRL-Fc Fc embryos stained with DRL-Fc

  27. embryos stained with DRL-Fc

  28. drl- embryos stained with DRL-Fc DRL-Fc immunoprecipitates WNT5

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