Receptor tyrosine phosphatases regulate axon guidance across the midline of the <i>Drosophila</i> embryo

Qi Sun, Sami Bahri, Aloisia Schmid, William Chia, Kai Zinn

Development · 2000 · 118 citations · 42 references

Concepts

TL;DR

Neural receptor‑linked protein tyrosine phosphatases (RPTPs) are essential for axon guidance in Drosophila, yet their specific roles in responding to guidance cues such as Slit/Robo signaling remain unclear. Mutations in the fourth neural RPTP, DPTP10D, together with DPTP69D, are required for Slit/Robo‑mediated repulsion of growth cones from the CNS midline, and loss of all four neural RPTPs converts most noncrossing longitudinal axons into commissures, demonstrating that tyrosine phosphorylation regulates midline guidance.

Abstract

ABSTRACT Neural receptor-linked protein tyrosine phosphatases (RPTPs) are required for guidance of motoneuron and photoreceptor growth cones in Drosophila. These phosphatases have not been implicated in growth cone responses to specific guidance cues, however, so it is unknown which aspects of axonal pathfinding are controlled by their activities. Three RPTPs, known as DLAR, DPTP69D, and DPTP99A, have been genetically characterized thus far. Here we report the isolation of mutations in the fourth neural RPTP, DPTP10D. The analysis of double mutant phenotypes shows that DPTP10D and DPTP69D are necessary for repulsion of growth cones from the midline of the embryonic central nervous system. Repulsion is thought to be triggered by binding of the secreted protein Slit, which is expressed by midline glia, to Roundabout (Robo) receptors on growth cones. Robo repulsion is downregulated by the Commissureless (Comm) protein, allowing axons to cross the midline. Here we show that the Rptp mutations genetically interact with robo, slit and comm. The nature of these interactions suggests that DPTP10D and DPTP69D are positive regulators of Slit/Roundabout repulsive signaling. We also show that elimination of all four neural RPTPs converts most noncrossing longitudinal pathways into commissures that cross the midline, indicating that tyrosine phosphorylation controls the manner in which growth cones respond to midline signals.

References

42