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ETS转录因子Erm控制骨骼肌突触下基因表达。

ETS transcription factor Erm controls subsynaptic gene expression in skeletal muscles.

作者信息

Hippenmeyer Simon, Huber Roland M, Ladle David R, Murphy Kenneth, Arber Silvia

机构信息

Biozentrum, Department of Cell Biology, University of Basel, Klingelbergstrasse 70, 4056 Basel, Switzerland.

出版信息

Neuron. 2007 Sep 6;55(5):726-40. doi: 10.1016/j.neuron.2007.07.028.

Abstract

Accumulation of specific proteins at synaptic structures is essential for synapse assembly and function, but mechanisms regulating local protein enrichment remain poorly understood. At the neuromuscular junction (NMJ), subsynaptic nuclei underlie motor axon terminals within extrafusal muscle fibers and are transcriptionally distinct from neighboring nuclei. In this study, we show that expression of the ETS transcription factor Erm is highly concentrated at subsynaptic nuclei, and its mutation in mice leads to severe downregulation of many genes with normally enriched subsynaptic expression. Erm mutant mice display an expansion of the muscle central domain in which acetylcholine receptor (AChR) clusters accumulate, show gradual fragmentation of AChR clusters, and exhibit symptoms of muscle weakness mimicking congenital myasthenic syndrome (CMS). Together, our findings define Erm as an upstream regulator of a transcriptional program selective to subsynaptic nuclei at the NMJ and underscore the importance of transcriptional control of local synaptic protein accumulation.

摘要

特定蛋白质在突触结构处的积累对于突触组装和功能至关重要,但调节局部蛋白质富集的机制仍知之甚少。在神经肌肉接头(NMJ)处,突触下核位于梭外肌纤维内运动轴突终末的下方,并且在转录上与相邻核不同。在本研究中,我们表明ETS转录因子Erm的表达高度集中于突触下核,其在小鼠中的突变导致许多通常在突触下高度表达的基因严重下调。Erm突变小鼠表现出肌肉中央区域的扩张,其中乙酰胆碱受体(AChR)簇聚集,AChR簇逐渐碎片化,并表现出类似于先天性肌无力综合征(CMS)的肌肉无力症状。总之,我们的研究结果将Erm定义为NMJ处突触下核选择性转录程序的上游调节因子,并强调了局部突触蛋白积累的转录控制的重要性。

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