Inhibition of <i>Cpeb3</i> ribozyme elevates CPEB3 protein expression and polyadenylation of its target mRNAs and enhances object location memory.
basic_science · Level V
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- Record sourced from PubMed, PMID 38319152.
- Also identified by DOI 10.7554/eLife.90116 and PMC identifier 10919898.
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Abstract
A self-cleaving ribozyme that maps to an intron of the cytoplasmic polyadenylation element-binding protein 3 (<i>Cpeb3</i>) 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 <i>Cpeb3</i> 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.
Medical subject headings
- RNA, Catalytic