Inhibition of Cpeb3 ribozyme elevates CPEB3 protein expression and polyadenylation of its target mRNAs and enhances object location memory

Author:

Chen Claire C1ORCID,Han Joseph2,Chinn Carlene A2,Rounds Jacob S2,Li Xiang2,Nikan Mehran3,Myszka Marie4,Tong Liqi5,Passalacqua Luiz FM1ORCID,Bredy Timothy2ORCID,Wood Marcelo A2,Luptak Andrej146ORCID

Affiliation:

1. Department of Pharmaceutical Sciences, University of California, Irvine

2. Department of Neurobiology and Behavior, Center for the Neurobiology of Learning and Memory, University of California, Irvine

3. Ionis Pharmaceuticals

4. Department of Chemistry, University of California, Irvine

5. Institute for Memory Impairments and Neurological Disorders, University of California, Irvine

6. Department of Molecular Biology and Biochemistry, University of California, Irvine

Abstract

A self-cleaving ribozyme that maps to an intron of the cytoplasmic polyadenylation element-binding protein 3 (Cpeb3) gene is thought to play a role in human episodic memory, but the underlying mechanisms mediating this effect are not known. We tested the activity of the murine sequence and found that the ribozyme’s self-scission half-life matches the time it takes an RNA polymerase to reach the immediate downstream exon, suggesting that the ribozyme-dependent intron cleavage is tuned to co-transcriptional splicing of the Cpeb3 mRNA. Our studies also reveal that the murine ribozyme modulates maturation of its harboring mRNA in both cultured cortical neurons and the hippocampus: inhibition of the ribozyme using an antisense oligonucleotide leads to increased CPEB3 protein expression, which enhances polyadenylation and translation of localized plasticity-related target mRNAs, and subsequently strengthens hippocampal-dependent long-term memory. These findings reveal a previously unknown role for self-cleaving ribozyme activity in regulating experience-induced co-transcriptional and local translational processes required for learning and memory.

Funder

National Institutes of Health

National Science Foundation

Publisher

eLife Sciences Publications, Ltd

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