The Journal of Neuroscience, April 15, 2003, 23(8):3415
Inhibition of Conditioned Stimulus Pathway Phosphoprotein
24 Expression Blocks the Development of Intermediate-Term Memory
in Hermissenda
Terry
Crow1,
John B.
Redell2,
Lian-Ming
Tian1,
Juan
Xue-Bian1, and
Pramod K.
Dash1, 2
1 Department of Neurobiology and Anatomy,
2 Vivian L. Smith Center for Neurologic Research,
University of Texas Medical School, Houston, Texas 77225
Studies of memory consolidation have identified multiple phases or
stages in the formation of memories. The multiple components of memory
can be broadly divided into the three phases; short-term, intermediate-term, and long-term. Although molecular changes
underlying short- and long-term memory have been examined extensively,
the molecular mechanisms supporting the formation of intermediate-term memory are poorly understood. In several examples of cellular and
synaptic plasticity, intermediate memory depends on translation but not
transcription. One-trial conditioning in Hermissenda
results in the development of intermediate memory that is associated
with enhanced cellular excitability and the phosphorylation of a 24 kDa
protein referred to as conditioned stimulus pathway phosphoprotein (Csp24). Using amino acid sequences derived from Csp24 peptide fragments, a full-length cDNA was cloned and shown to contain multiple
-thymosin-like domains. The expression of Csp24 and the development
of enhanced excitability, a characteristic of intermediate memory, were
blocked by antisense oligonucleotide-mediated downregulation of Csp24
without affecting the induction of immediate enhanced excitability, a
characteristic of short-term memory. These results demonstrate that the
synthesis of Csp24 is required for the development and maintenance of
intermediate memory.
Key words:
Hermissenda; Csp24;
-thymosin
repeat protein; one-trial Pavlovian conditioning; actin-binding
proteins; cytoskeleton
Copyright © 2003 Society for Neuroscience 0270-6474/03/2383415-08$05.00/0