Kinesin mRNA is present in the squid giant axon

J Neurochem. 1994 Jul;63(1):13-8. doi: 10.1046/j.1471-4159.1994.63010013.x.

Abstract

Recently, we reported the construction of a cDNA library encoding a heterogeneous population of polyadenylated mRNAs present in the squid giant axon. The nucleic acid sequencing of several randomly selected clones led to the identification of cDNAs encoding beta-actin and beta-tubulin, two relatively abundant axonal mRNA species. To continue characterization 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 unambiguously identified axonal kinesin cDNA clones. The axonal localization of kinesin mRNA was subsequently verified by in situ hybridization histochemistry. In addition, the presence of kinesin RNA sequences in the axoplasmic polyribosome fraction was demonstrated using PCR methodology. In contrast to these findings, mRNA encoding the squid sodium channel was not detected in axoplasmic RNA, although these sequences were relatively abundant in the giant fiber lobe. Taken together, these findings 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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / analysis
  • Actins / genetics
  • Amino Acid Sequence
  • Animals
  • Axons / chemistry*
  • Base Sequence
  • DNA / analysis
  • DNA / genetics
  • Decapodiformes
  • In Situ Hybridization
  • Kinesins / genetics*
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • RNA, Messenger / analysis*
  • RNA, Messenger / genetics
  • Tubulin / analysis
  • Tubulin / genetics

Substances

  • Actins
  • RNA, Messenger
  • Tubulin
  • DNA
  • Kinesins