Zoological Institute, Technical University Braunschweig, Braunschweig, Germany
Martin Korte
Zoological Institute, Technical University Braunschweig, Braunschweig, Germany; AG Neuroinflammation and Neurodegeneration (NIND), Braunschweig, Germany
Gaurav Jain
Research Group for Epigenetics in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases, Göttingen, Germany; Research Group for Complex Neurodegenerative Disorders, German Center for Neurodegenerative Diseases, Göttingen, Germany
Andre Fischer
Research Group for Epigenetics in Neurodegenerative Diseases, German Center for Neurodegenerative Diseases, Göttingen, Germany; Department of Psychiatry and Psychotherapy, University Medical Center, German Center for Neurodegenerative Diseases, Göttingen, Germany
Farahnaz Sananbenesi
Research Group for Complex Neurodegenerative Disorders, German Center for Neurodegenerative Diseases, Göttingen, Germany
Isabella Cera
Institute for Neuroscience, Medical University of Innsbruck, Innsbruck, Austria
Nicolas Singewald
Department of Pharmacology and Toxicology, University of Innsbruck, Innsbruck, Austria
Georg Dechant
Institute for Neuroscience, Medical University of Innsbruck, Innsbruck, Austria
SATB2 is a risk locus for schizophrenia and encodes a DNA-binding protein that regulates higher-order chromatin configuration. In the adult brain Satb2 is almost exclusively expressed in pyramidal neurons of two brain regions important for memory formation, the cerebral cortex and the CA1-hippocampal field. Here we show that Satb2 is required for key hippocampal functions since deletion of Satb2 from the adult mouse forebrain prevents the stabilization of synaptic long-term potentiation and markedly impairs long-term fear and object discrimination memory. At the molecular level, we find that synaptic activity and BDNF up-regulate Satb2, which itself binds to the promoters of coding and non-coding genes. Satb2 controls the hippocampal levels of a large cohort of miRNAs, many of which are implicated in synaptic plasticity and memory formation. Together, our findings demonstrate that Satb2 is critically involved in long-term plasticity processes in the adult forebrain that underlie the consolidation and stabilization of context-linked memory.