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PIASx是一种MEF2 SUMO E3连接酶,可促进突触后树突形态发生。

PIASx is a MEF2 SUMO E3 ligase that promotes postsynaptic dendritic morphogenesis.

作者信息

Shalizi Aryaman, Bilimoria Parizad M, Stegmüller Judith, Gaudillière Brice, Yang Yue, Shuai Ke, Bonni Azad

机构信息

Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

J Neurosci. 2007 Sep 12;27(37):10037-46. doi: 10.1523/JNEUROSCI.0361-07.2007.

Abstract

Postsynaptic morphogenesis of dendrites is essential for the establishment of neural connectivity in the brain, but the mechanisms that govern postsynaptic dendritic differentiation remain poorly understood. Sumoylation of the transcription factor myocyte enhancer factor 2A (MEF2A) promotes the differentiation of postsynaptic granule neuron dendritic claws in the cerebellar cortex. Here, we identify the protein PIASx as a MEF2 SUMO E3 ligase that represses MEF2-dependent transcription in neurons. Gain-of-function and genetic knockdown experiments in rat cerebellar slices and in the postnatal cerebellum in vivo reveal that PIASx drives the differentiation of granule neuron dendritic claws in the cerebellar cortex. MEF2A knockdown suppresses PIASx-induced dendritic claw differentiation, and expression of sumoylated MEF2A reverses PIASx knockdown-induced loss of dendritic claws. These findings define the PIASx-MEF2 sumoylation signaling link as a key mechanism that orchestrates postsynaptic dendritic claw morphogenesis in the cerebellar cortex and suggest novel functions for SUMO E3 ligases in brain development and plasticity.

摘要

树突的突触后形态发生对于大脑中神经连接的建立至关重要,但控制突触后树突分化的机制仍知之甚少。转录因子肌细胞增强因子2A(MEF2A)的SUMO化促进小脑皮质中突触后颗粒神经元树突爪的分化。在这里,我们确定蛋白质PIASx为一种MEF2 SUMO E3连接酶,它在神经元中抑制MEF2依赖的转录。在大鼠小脑切片和出生后体内小脑中进行的功能获得和基因敲低实验表明,PIASx驱动小脑皮质中颗粒神经元树突爪的分化。MEF2A敲低抑制PIASx诱导的树突爪分化,而SUMO化MEF2A的表达逆转PIASx敲低诱导的树突爪丧失。这些发现将PIASx-MEF2 SUMO化信号传导联系定义为协调小脑皮质中突触后树突爪形态发生的关键机制,并提示SUMO E3连接酶在大脑发育和可塑性中的新功能。

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