Jaitner Clemens, Reddy Chethan, Abentung Andreas, Whittle Nigel, Rieder Dietmar, Delekate Andrea, Korte Martin, Jain Gaurav, Fischer Andre, Sananbenesi Farahnaz, Cera Isabella, Singewald Nicolas, Dechant Georg, Apostolova Galina
Institute for Neuroscience, Medical University of Innsbruck, Innsbruck, Austria.
Department of Pharmacology and Toxicology, University of Innsbruck, Innsbruck, Austria.
Elife. 2016 Nov 29;5:e17361. doi: 10.7554/eLife.17361.
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.
是精神分裂症的一个风险位点,编码一种调节高阶染色质构型的DNA结合蛋白。在成人大脑中,Satb2几乎仅在对记忆形成很重要的两个脑区的锥体神经元中表达,即大脑皮层和CA1海马区。我们在此表明,Satb2是海马关键功能所必需的,因为从成年小鼠前脑删除Satb2会阻止突触长期增强的稳定,并显著损害长期恐惧和物体辨别记忆。在分子水平上,我们发现突触活动和脑源性神经营养因子(BDNF)上调Satb2,而Satb2本身与编码基因和非编码基因的启动子结合。Satb2控制大量微小RNA(miRNA)的海马水平,其中许多与突触可塑性和记忆形成有关。总之,我们的研究结果表明,Satb2在成体前脑的长期可塑性过程中起关键作用,这些过程是情境关联记忆巩固和稳定的基础。