Agrin is a synapse-organizing protein likely to mediate nerve-induced
aggregation of acetylcholine receptors and other postsynaptic componen
ts at the neuromuscular junction. We used in situ hybridization and po
lymerase chain reaction (PCR) to define the localization of agrin mRNA
and its alternatively spliced forms in the chick embryo nervous syste
m. Agrin cRNA probes intensely labeled motor neurons, dorsal root gang
lia, cerebellar Purkinje neurons, and retinal ganglion cells. Neuronal
layers in optic tectum and ventricular regions were also labeled. Ana
lysis by PCR showed that all parts of the nervous system at embryonic
day 10 contained three major forms of agrin mRNA. Our results raise th
e possibility that agrin isoforms play a role in synapse formation or
other aspects of neuronal development in the central nervous system.