Recently, we reported the construction of a cDNA library encoding a he
terogeneous population of polyadenylated mRNAs present in the squid gi
ant axon. The nucleic acid sequencing of several randomly selected clo
nes led to the identification of cDNAs encoding beta-actin and beta-tu
bulin, two relatively abundant axonal mRNA species. To continue charac
terization of this unique mRNA population, the axonal cDNA library was
screened with a cDNA probe encoding the carboxy terminus of the squid
kinesin heavy chain. The sequencing of several positive clones unambi
guously identified axonal kinesin cDNA clones. The axonal localization
of kinesin mRNA was subsequently verified by in situ hybridization hi
stochemistry. In addition, the presence of kinesin RNA sequences in th
e axoplasmic polyribosome fraction was demonstrated using PCR methodol
ogy. In contrast to these findings, mRNA encoding the squid sodium cha
nnel was not detected in axoplasmic RNA, although these sequences were
relatively abundant in the giant fiber lobe. Taken together, these fi
ndings demonstrate that kinesin mRNA is a component of a select group
of mRNAs present in the squid giant axon, and suggest that kinesin may
be synthesized locally in this model invertebrate motor neuron.