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Branching microtubule nucleation in xenopus egg extracts mediated by augmin and TPX2

机译:augmin和TPX2介导的非洲爪蟾卵提取物中的分支微管成核

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摘要

The microtubules that comprise mitotic spindles in animal cells are nucleated at centrosomes and by spindle assembly factors that are activated in the vicinity of chromatin. Indirect evidence has suggested that microtubules also might be nucleated from pre-existing microtubules throughout the spindle, but this process has not been observed directly. Here, we demonstrate microtubule nucleation from the sides of existing microtubules in meiotic Xenopus egg extracts. Daughter microtubules grow at a low branch angle and with the same polarity as mother filaments. Branching microtubule nucleation requires γ-tubulin and augmin and is stimulated by factors previously implicated in chromatin-stimulated nucleation, guanosine triphosphate(GTP)-bound Ran and its effector, TPX2. Because of the rapid amplification of microtubule numbers and the preservation of microtubule polarity, microtubule-dependent microtubule nucleation is well suited for spindle assembly and maintenance.
机译:在动物细胞中包含有丝分裂纺锤体的微管在中心体处被成核,并通过在染色质附近被激活的纺锤体装配因子成核。间接证据表明,微管也可能由于整个纺锤体中已存在的微管而成核,但尚未直接观察到此过程。在这里,我们从减数分裂爪蟾卵提取物中现有微管的侧面展示了微管成核。子微管以低分支角和与母丝相同的极性生长。分支微管成核需要γ-微管蛋白和augmin,并受先前与染色质刺激成核,鸟苷三磷酸(GTP)结合的Ran及其效应物TPX2有关。由于微管数量的快速扩增和微管极性的保留,微管依赖性微管成核非常适合纺锤体组装和维护。

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