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PMID:15269269

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Citation

Franco, B, Bogdanik, L, Bobinnec, Y, Debec, A, Bockaert, J, Parmentier, ML and Grau, Y (2004) Shaggy, the homolog of glycogen synthase kinase 3, controls neuromuscular junction growth in Drosophila. J. Neurosci. 24:6573-7

Abstract

A protein-trap screen using the Drosophila neuromuscular junction (NMJ) as a model synapse was performed to identify genes that control synaptic structure or plasticity. We found that Shaggy (Sgg), the Drosophila homolog of the mammalian glycogen synthase kinases 3 alpha and beta, two serine-threonine kinases, was concentrated at this synapse. Using various combinations of mutant alleles of shaggy, we found that Shaggy negatively controlled the NMJ growth. Moreover, tissue-specific expression of a dominant-negative Sgg indicated that this kinase is required in the motoneuron, but not in the muscle, to control NMJ growth. Finally, we show that Sgg controlled the microtubule cytoskeleton dynamics in the motoneuron and that Futsch, a microtubule-associated protein, was required for Shaggy function on synaptic growth.

Links

PubMed Online version:10.1523/JNEUROSCI.1580-04.2004

Keywords

Animals; Drosophila Proteins/analysis; Drosophila Proteins/genetics; Drosophila Proteins/physiology; Drosophila melanogaster/enzymology; Drosophila melanogaster/growth & development; Drosophila melanogaster/ultrastructure; Glycogen Synthase Kinase 3/analysis; Glycogen Synthase Kinase 3/genetics; Glycogen Synthase Kinase 3/physiology; Larva/enzymology; Microtubule-Associated Proteins/genetics; Microtubules/ultrastructure; Motor Neurons/enzymology; Mutation; Nerve Growth Factors/genetics; Neuromuscular Junction/enzymology; Neuromuscular Junction/growth & development; Neuronal Plasticity; Presynaptic Terminals/enzymology; Presynaptic Terminals/ultrastructure

Significance

Annotations

Gene product Qualifier GO ID GO term name Evidence Code with/from Aspect Notes Status


See also

References

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