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首页> 外文期刊>Developmental cell >Amphiphysin 2 Orchestrates Nucleus Positioning and Shape by Linking the Nuclear Envelope to the Actin and Microtubule Cytoskeleton
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Amphiphysin 2 Orchestrates Nucleus Positioning and Shape by Linking the Nuclear Envelope to the Actin and Microtubule Cytoskeleton

机译:Amphiphysin 2通过将核信封连接到肌动蛋白和微管细胞骨架上来协调细胞核的位置和形状。

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摘要

Nucleus positioning is key for intracellular organization, cell differentiation, and organ development and is affected in many diseases, including myopathies due to alteration in amphiphysin-2 (BIN1). The actin and microtubule cytoskeletons are essential for nucleus positioning, but their crosstalk in this process is sparsely characterized. Here, we report that impairment of amphiphysin/BIN1 in Caenorhabditis elegans, mammalian cells, or muscles from patients with centronuclear myopathy alters nuclear position and shape. We show that AMPH-1/BIN1 binds to nesprin and actin, as well as to the microtubule-binding protein CLIP170 in both species. Expression of the microtubule-anchoring CAP-GLY domain of CLIP170 fused to the nuclear-envelope-anchoring KASH domain of nesprin rescues nuclear positioning defects of amph-1 mutants. Amphiphysins thus play a central role in linking the nuclear envelope with the actin and microtubule cytoskeletons. We propose that BIN1 has a direct and evolutionarily conserved role in nuclear positioning, altered in myopathies.
机译:核定位是细胞内组织,细胞分化和器官发育的关键,并且在许多疾病中都受到影响,包括由于两性纤维蛋白2(BIN1)的改变而引起的肌病。肌动蛋白和微管细胞骨架对于细胞核定位至关重要,但是在此过程中它们的串扰很少被表征。在这里,我们报告说,秀丽隐杆线虫,哺乳动物细胞或中心核肌病患者的肌肉中的两亲/双功能障碍会改变核的位置和形状。我们表明,AMPH-1 / BIN1绑定到nesprin和肌动蛋白,以及在两个物种中的微管结合蛋白CLIP170。将CLIP170的微管锚定CAP-GLY域与内斯普林的核膜锚定KASH域融合表达可挽救amph-1突变体的核定位缺陷。因此,两亲菌素在连接核膜与肌动蛋白和微管细胞骨架中起着核心作用。我们提议BIN1在肌病中改变的核定位中具有直接和进化上保守的作用。

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