CBP Is Required for Establishing Adaptive Gene Programs in the Adult Mouse Brain

• Published in: The Journal of neuroscience Vol. 42; no. 42; pp. 7984 - 8001
• Main Authors: Lipinski, Michal, Niñerola, Sergio, Fuentes-Ramos, Miguel, Valor, Luis M, Del Blanco, Beatriz, López-Atalaya, Jose P, Barco, Angel
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 19.10.2022
• Subjects: Acetylation; Animals; Brain; Chromatin; Chromatin - metabolism; Circuits; Cognitive ability; CREB-Binding Protein - genetics; CREB-Binding Protein - metabolism; Cyclic AMP response element-binding protein; Enrichment; Environmental conditions; Environmental factors; Epigenesis, Genetic; Epigenetics; Female; Forebrain; Hippocampus; Hippocampus - metabolism; Histone Acetyltransferases - metabolism; Histones; Histones - metabolism; Intellectual disabilities; Kindling; Lysine; Male; Mice; Molecular modelling; Nervous system; Neural plasticity; Neurons; p300-CBP Transcription Factors - genetics; p300-CBP Transcription Factors - metabolism; Proteins; Transcription; Transcription Factors - metabolism; CBP; p300; activity-driven transcription; neuroepigenetics; lysine acetylation; intellectual disability
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/JNEUROSCI.0970-22.2022

Environmental factors and life experiences impinge on brain circuits triggering adaptive changes. Epigenetic regulators contribute to this neuroadaptation by enhancing or suppressing specific gene programs. The paralogous transcriptional coactivators and lysine acetyltransferases CREB binding protein (CBP) and p300 are involved in brain plasticity and stimulus-dependent transcription, but their specific roles in neuroadaptation are not fully understood. Here we investigated the impact of eliminating either CBP or p300 in excitatory neurons of the adult forebrain of mice from both sexes using inducible and cell type-restricted knock-out strains. The elimination of CBP, but not p300, reduced the expression and chromatin acetylation of plasticity genes, dampened activity-driven transcription, and caused memory deficits. The defects became more prominent in elderly mice and in paradigms that involved enduring changes in transcription, such as kindling and environmental enrichment, in which CBP loss interfered with the establishment of activity-induced transcriptional and epigenetic changes in response to stimulus or experience. These findings further strengthen the link between CBP deficiency in excitatory neurons and etiopathology in the nervous system. How environmental conditions and life experiences impinge on mature brain circuits to elicit adaptive responses that favor the survival of the organism remains an outstanding question in neurosciences. Epigenetic regulators are thought to contribute to neuroadaptation by initiating or enhancing adaptive gene programs. In this article, we examined the role of CREB binding protein (CBP) and p300, two paralogous transcriptional coactivators and histone acetyltransferases involved in cognitive processes and intellectual disability, in neuroadaptation in adult hippocampal circuits. Our experiments demonstrate that CBP, but not its paralog p300, plays a highly specific role in the epigenetic regulation of neuronal plasticity gene programs in response to stimulus and provide unprecedented insight into the molecular mechanisms underlying neuroadaptation.