Román Olivares, Juan Medrano-Relinque, Angel Barco, Rafael Muñoz-Viana, Grzegorz M. Wilczynski, Angel Marquez-Galera, Santiago Canals, Carmen M. Navarrón, Jordi Fernandez-Albert, Beatriz del Blanco, José P. López-Atalaya, Michal Lipinski, José M. Caramés, Andrzej A. Szczepankiewicz, Ministerio de Ciencia, Innovación y Universidades (España), Ministerio de Economía y Competitividad (España), Agencia Estatal de Investigación (España), European Commission, Generalitat Valenciana, Polish Academy of Sciences, Ministerio de Educación, Cultura y Deporte (España), Lipinski, Michal [0000-0001-8200-5056], Muñoz-Viana, Rafael [0000-0002-1363-6978], Szczepankiewicz, Andrzej A. [0000-0002-1502-3147], Navarrón, Carmen M. [0000-0002-6304-3695], Canals Gamoneda, Santiago [0000-0003-2175-8139], Barco, Ángel [0000-0002-0653-3751], Lipinski, Michal, Muñoz-Viana, Rafael, Szczepankiewicz, Andrzej A., Navarrón, Carmen M., Canals Gamoneda, Santiago, and Barco, Ángel
The lysine acetyltransferases type 3 (KAT3) family members CBP and p300 are important transcriptional co-activators, but their specific functions in adult post-mitotic neurons remain unclear. Here, we show that the combined elimination of both proteins in forebrain excitatory neurons of adult mice resulted in a rapidly progressing neurological phenotype associated with severe ataxia, dendritic retraction and reduced electrical activity. At the molecular level, we observed the downregulation of neuronal genes, as well as decreased H3K27 acetylation and pro-neural transcription factor binding at the promoters and enhancers of canonical neuronal genes. The combined deletion of CBP and p300 in hippocampal neurons resulted in the rapid loss of neuronal molecular identity without de- or transdifferentiation. Restoring CBP expression or lysine acetylation rescued neuronal-specific transcription in cultured neurons. Together, these experiments show that KAT3 proteins maintain the excitatory neuron identity through the regulation of histone acetylation at cell type-specific promoter and enhancer regions., M.L. is recipient of a Santiago Grisolia fellowship given by the Generalitat Valenciana, J.M.C. is recipient of a fellowship from the Spanish Ministry of Education, Culture and Sport (MECD), J.F.-A. and C.M.N. are recipients of fellowships from the Spanish Ministry of Science and Innovation (MICINN). The ultrastructure research was supported by the Polish National Science Center Grant UMO-2014/15/N/NZ3/04468 and by the European Regional Development Fund POIG 01.01.02-00-008/08. J.P.L.-A. research is supported by Grants RYC-2015-18056 and RTI2018-102260-B-I00 from MICINN co-financed by ERDF. A.B. research is supported by Grants SAF2017-87928-R, PCIN-2015-192-C02-01, and SEV-2017-0723 from MICINN co-financed by ERDF, PROMETEO/2016/026 from the Generalitat Valenciana, and RGP0039/2017 from the Human Frontiers Science Program Organization (HFSPO). The Instituto de Neurociencias is a “Centre of Excellence Severo Ochoa”.