Journal of Neuroscience · 2009 · 13 citations · 51 references
MedicineNeurobiologyNeuroscienceBehavioral NeuroscienceMolecular NeurobiologyMolecular NeuroscienceLearning In Neural SystemsMemory ConsolidationMemory EncodingNeural Basis Of MemoryCentral Sensory ProcessingFlap Endonuclease 1 ProcessingLong-term Memory ConsolidationMemory MechanismsMolecular Mechanisms Of MemoryRecombination Repair PathwaysStructure-specific EndonucleasesTaste Aversion Learning
We previously proposed that DNA recombination/repair processes play a role in memory formation. Here, we examined the possible role of the fen-1 gene, encoding a flap structure-specific endonuclease, in memory consolidation of conditioned taste aversion (CTA). Quantitative real-time PCR showed that amygdalar fen-1 mRNA induction was associated to the central processing of the illness experience related to CTA and to CTA itself, but not to the central processing resulting from the presentation of a novel flavor. CTA also increased expression of the Fen-1 protein in the amygdala, but not the insular cortex. In addition, double immunofluorescence analyses showed that amygdalar Fen-1 expression is mostly localized within neurons. Importantly, functional studies demonstrated that amygdalar antisense knockdown of fen-1 expression impaired consolidation, but not short-term memory, of CTA. Overall, these studies define the fen-1 endonuclease as a new DNA recombination/repair factor involved in the formation of long-term memories.
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