Long time no single word on MuSK program progress.
Here is something, to think that they have moved bit further.
© The Rockefeller University Press, The Journal of Cell Biology, Volume 146, Number 5, September 6, 1999 1133-1146
Distinct Domains of MuSK Mediate Its Abilities to Induce and to Associate with Postsynaptic Specializations
Heather Zhoua, David J. Glassb, George D. Yancopoulosb, and Joshua R. Sanesa
a Washington University School of Medicine, St. Louis, Missouri 63110
b Regeneron Pharmaceuticals, Tarrytown, New York 10591
Correspondence to: Joshua R. Sanes, Department of Anatomy and Neurobiology, Washington University School of Medicine, 660 South Euclid Avenue, Box 8108, St. Louis, MO 63110. Tel:(314) 362-2507 Fax:(314) 747-1150 E-mail:sanesj@thalamus.wustl.edu.
Agrin released from motor nerve terminals activates a muscle-specific receptor tyrosine kinase (MuSK) in muscle cells to trigger formation of the skeletal neuromuscular junction. A key step in synaptogenesis is the aggregation of acetylcholine receptors (AChRs) in the postsynaptic membrane, a process that requires the AChR-associated protein, rapsyn. Here, we mapped domains on MuSK necessary for its interactions with agrin and rapsyn. Myotubes from MuSK-/- mutant mice form no AChR clusters in response to agrin, but agrin-responsiveness is restored by the introduction of rat MuSK or a Torpedo orthologue. Thus, MuSK-/- myotubes provide an assay system for the structure–function analysis of MuSK. Using this system, we found that sequences in or near the first of four extracellular immunoglobulin-like domains in MuSK are required for agrin responsiveness, whereas sequences in or near the fourth immunoglobulin-like domain are required for interaction with rapsyn. Analysis of the cytoplasmic domain revealed that a recognition site for the phosphotyrosine binding domain–containing proteins is essential for MuSK activity, whereas consensus binding sites for the PSD-95/Dlg/ZO-1-like domain–containing proteins and phosphatidylinositol-3-kinase are dispensable. Together, our results indicate that the ectodomain of MuSK mediates both agrin- dependent activation of a complex signal transduction pathway and agrin-independent association of the kinase with other postsynaptic components. These interactions allow MuSK not only to induce a multimolecular AChR-containing complex, but also to localize that complex to a primary scaffold in the postsynaptic membrane.
Key Words: MuSK, acetylcholine receptors, neuromuscular junction, synapse, agrin
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