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首页> 外文期刊>Neuron >Drosophila ankyrin 2 is required for synaptic stability.
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Drosophila ankyrin 2 is required for synaptic stability.

机译:果蝇锚蛋白2是突触稳定性所必需的。

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摘要

Synaptic connections are stabilized through transsynaptic adhesion complexes that are anchored in the underlying cytoskeleton. The Drosophila neuromuscular junction (NMJs) serves as a model system to unravel genes required for the structural remodeling of synapses. In a mutagenesis screen for regulators of synaptic stability, we recovered mutations in Drosophila ankyrin 2 (ank2) affecting two giant Ank2 isoforms that are specifically expressed in the nervous system and associate with the presynaptic membrane cytoskeleton. ank2 mutant larvae show severe deficits in the stability of NMJs, resulting in a reduction in overall terminal size, withdrawal of synaptic boutons, and disassembly of presynaptic active zones. In addition, lack of Ank2 leads to disintegration of the synaptic microtubule cytoskeleton. Microtubules and microtubule-associated proteins fail to extend into distant boutons. Interestingly, Ank2 functions downstream of spectrin in the anchorage of synaptic microtubules, providing the cytoskeletal scaffold that is essential for synaptic stability.
机译:突触连接通过锚定在下面的细胞骨架中的跨突触粘附复合物来稳定。果蝇神经肌肉接头(NMJs)作为模型系统来揭示突触结构重塑所需的基因。在针对突触稳定性调节剂的诱变筛选中,我们恢复了果蝇锚蛋白2(ank2)中的突变,这些突变影响了两个在神经系统中特异性表达的巨型Ank2同工型,并与突触前膜细胞骨架相关。 ank2突变幼虫在NMJs的稳定性中显示出严重的缺陷,从而导致总末端大小的减少,突触钮扣的撤出以及突触前活性区的拆卸。此外,缺乏Ank2会导致突触微管细胞骨架解体。微管和与微管相关的蛋白质无法延伸到远处的按钮。有趣的是,Ank2在突触微管的锚固中血影蛋白的下游起作用,提供了对突触稳定性必不可少的细胞骨架支架。

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