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Nuclear movement during myotube formation is microtubule and dynein dependent and is regulated by Cdc42 Par6 and Par3

机译:肌管形成过程中的核运动取决于微管和动力蛋白并受Cdc42Par6和Par3调控

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摘要

Cells actively position their nucleus within the cytoplasm. One striking example is observed during skeletal myogenesis. Differentiated myoblasts fuse to form a multinucleated myotube with nuclei positioned in the centre of the syncytium by an unknown mechanism. Here, we describe that the nucleus of a myoblast moves rapidly after fusion towards the central myotube nuclei. This movement is driven by microtubules and dynein/dynactin complex, and requires Cdc42, Par6 and Par3. We found that Par6β and dynactin accumulate at the nuclear envelope of differentiated myoblasts and myotubes, and this accumulation is dependent on Par6 and Par3 proteins but not on microtubules. These results suggest a mechanism where nuclear movement after fusion is driven by microtubules that emanate from one nucleus that are pulled by dynein/dynactin complex anchored to the nuclear envelope of another nucleus.
机译:细胞将细胞核主动定位在细胞质内。在骨骼肌发生过程中观察到一个惊人的例子。分化的成肌细胞融合形成多核肌管,其核通过未知机制位于合胞体中心。在这里,我们描述成肌细胞的核向中央肌管核融合后迅速移动。这种运动是由微管和动力蛋白/动力蛋白复合物驱动的,需要Cdc42,Par6和Par3。我们发现Par6β和dynactin聚集在分化的成肌细胞和肌管的核膜上,并且这种聚集依赖于Par6和Par3蛋白,而不是微管。这些结果表明了一种机制,其中融合后的核运动由一个核发出的微管驱动,微管由固定在另一核的核膜上的动力蛋白/动力蛋白复合物拉动。

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