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Article
Nature Neuroscience  7, 1303 - 1309 (2004)
Published online: 14 November 2004; | doi:10.1038/nn1350

Zebrafish unplugged reveals a role for muscle-specific kinase homologs in axonal pathway choice

Jing Zhang1, 2, 3, Julie L Lefebvre1, 3, Shuxia Zhao1, 3 & Michael Granato1

1  Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6058, USA.

2  Present address: Whitehead Institute for Biomedical Research, Cambridge, Massachusetts, USA.

3  These authors contributed equally to this work.

Correspondence should be addressed to Michael Granato granatom@mail.med.upenn.edu
En route to their target, pioneering motor growth cones repeatedly encounter choice points at which they make pathway decisions. In the zebrafish mutant unplugged, two of the three segmental motor axons make incorrect decisions at a somitic choice point. Using positional cloning, we show here that unplugged encodes a homolog of muscle-specific kinase (MuSK) and that, unlike mammalian MuSK, unplugged has only a limited role in neuromuscular synaptogenesis. We demonstrate that unplugged is transiently expressed in cells adjacent to the choice point and that unplugged signaling before the arrival of growth cones induces changes in the extracellular environment. In addition, we find that the unplugged locus generates three different transcripts. The splice variant 1 (SV1) isoform lacks the extracellular modules essential for agrin responsiveness, and signaling through this isoform mediates axonal pathfinding, independent of the MuSK downstream component rapsyn. Our results demonstrate a new role for MuSK homologs in axonal pathway selection.

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Nature Neuroscience
ISSN: 1097-6256
EISSN: 1546-1726
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