Shalizi Aryaman, Gaudillière Brice, Yuan Zengqiang, Stegmüller Judith, Shirogane Takahiro, Ge Qingyuan, Tan Yi, Schulman Brenda, Harper J Wade, Bonni Azad
Department of Pathology, Harvard Medical School, 77 Louis Pasteur Avenue, Boston, MA 02115, USA.
Science. 2006 Feb 17;311(5763):1012-7. doi: 10.1126/science.1122513.
Postsynaptic differentiation of dendrites is an essential step in synapse formation. We report here a requirement for the transcription factor myocyte enhancer factor 2A (MEF2A) in the morphogenesis of postsynaptic granule neuron dendritic claws in the cerebellar cortex. A transcriptional repressor form of MEF2A that is sumoylated at lysine-403 promoted dendritic claw differentiation. Activity-dependent calcium signaling induced a calcineurin-mediated dephosphorylation of MEF2A at serine-408 and, thereby, promoted a switch from sumoylation to acetylation at lysine-403, which led to inhibition of dendritic claw differentiation. Our findings define a mechanism underlying postsynaptic differentiation that may modulate activity-dependent synapse development and plasticity in the brain.
树突的突触后分化是突触形成的关键步骤。我们在此报告,转录因子肌细胞增强因子2A(MEF2A)对小脑皮质中突触后颗粒神经元树突爪的形态发生是必需的。一种在赖氨酸-403处被SUMO化的MEF2A转录抑制形式促进了树突爪的分化。依赖活性的钙信号诱导钙调神经磷酸酶介导的MEF2A在丝氨酸-408处去磷酸化,从而促进赖氨酸-403处从SUMO化向乙酰化的转变,这导致树突爪分化受到抑制。我们的研究结果确定了一种突触后分化的潜在机制,该机制可能调节大脑中依赖活性的突触发育和可塑性。