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Syne proteins anchor muscle nuclei at the neuromuscular junction

机译:Syne蛋白将肌肉核锚定在神经肌肉接头处

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摘要

Vertebrate skeletal muscle fibers contain hundreds of nuclei, of which three to six are functionally specialized and stably anchored beneath the postsynaptic membrane at the neuromuscular junction (NMJ). The mechanisms that localize synaptic nuclei and the roles they play in neuromuscular development are unknown. Syne-1 is concentrated at the nuclear envelope of synaptic nuclei; its Caenorhabditis elegans orthologue ANC-1 functions to tether nuclei to the cytoskeleton. To test the involvement of Syne proteins in nuclear anchoring, we generated transgenic mice overex-pressing the conserved C-terminal Klarsicht/ANC-1/Syne homol-ogy domain of Syne-1. The transgene acted in a dominant interfering fashion, displacing endogenous Syne-1 from the nuclear envelope. Muscle nuclei failed to aggregate at the NMJ in transgenic mice, demonstrating that localization and positioning of synaptic nuclei require Syne proteins. We then exploited this phenotype to show that synaptic nuclear aggregates are dispensable for maturation of the NMJ.
机译:椎骨骨骼肌纤维包含数百个核,其中三到六个是功能特定的并且稳定地锚定在神经肌肉接头(NMJ)的突触后膜下方。定位突触核的机制及其在神经肌肉发育中的作用尚不清楚。 Syne-1集中在突触核的核膜上。它的秀丽隐杆线虫直系同源物ANC-1的功能是将细胞核束缚在细胞骨架上。为了测试Syne蛋白在核锚定中的参与,我们生成了过表达保守的Syne-1的C末端Klarsicht / ANC-1 / Syne同源结构域的转基因小鼠。转基因以显性干扰方式起作用,从核被膜中置换出内源性Syne-1。在转基因小鼠中,肌肉核未能聚集在NMJ处,表明突触核的定位和定位需要Syne蛋白。然后,我们利用该表型来显示突触核聚集体是NMJ成熟所不可或缺的。

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