Login / Signup

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

Claire C ChenJoseph HanCarlene A ChinnJacob S RoundsXiang LiMehran NikanMarie MyszkaLiqi TongLuiz F M PassalacquaTimothy W BredyMarcelo A WoodAndrej Lupták
Published in: eLife (2024)
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.
Keyphrases
  • binding protein
  • working memory
  • endothelial cells
  • genome wide
  • transcription factor
  • single cell
  • high glucose
  • spinal cord
  • spinal cord injury
  • dna methylation
  • drug induced
  • oxidative stress
  • copy number
  • nucleic acid