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A calcium-regulated MEF2 sumoylation switch controls postsynaptic differentiation.

机译:钙调节的MEF2磺酰化开关控制突触后的分化。

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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.
机译:突触后的树突分化是突触形成的重要步骤。我们在这里报告小脑皮层中突触后颗粒神经元树突爪的形态发生中转录因子肌细胞增强因子2A(MEF2A)的需求。 MEF2A的转录阻抑物形式在赖氨酸403处被Suoylated促进树突状爪分化。依赖于活性的钙信号传导诱导了钙调神经磷酸酶介导的丝氨酸408上MEF2A的去磷酸化,从而促进了赖氨酸403上的从SUMO化到乙酰化的转变,从而抑制了树突状爪的分化。我们的发现定义了一种突触后分化基础的机制,该机制可调节脑中活动依赖性突触的发育和可塑性。

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