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TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis

机译:TPXL-1在胞质分裂过程中激活Aurora A以清除极皮层的收缩环成分

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摘要

During cytokinesis, a signal from the central spindle that forms between the separating anaphase chromosomes promotes the accumulation of contractile ring components at the cell equator, while a signal from the centrosomal microtubule asters inhibits accumulation of contractile ring components at the cell poles. However, the molecular identity of the inhibitory signal has remained unknown. To identify molecular components of the aster-based inhibitory signal, we developed a means to monitor the removal of contractile ring proteins from the polar cortex after anaphase onset. Using this assay, we show that polar clearing is an active process that requires activation of Aurora A kinase by TPXL-1. TPXL-1 concentrates on astral microtubules coincident with polar clearing in anaphase, and its ability to recruit Aurora A and activate its kinase activity are essential for clearing. In summary, our data identify Aurora A kinase as an aster-based inhibitory signal that restricts contractile ring components to the cell equator during cytokinesis.
机译:在胞质分裂过程中,在分离的后期染色体之间形成的来自中心纺锤体的信号促进了收缩性环成分在细胞赤道处的积累,而来自中心微管紫苑的信号抑制了收缩性环成分在细胞两极的积累。然而,抑制信号的分子同一性仍然未知。为了确定基于紫aster的抑制信号的分子成分,我们开发了一种方法,用于监测后期发病后从极皮层中去除收缩环蛋白的方法。使用该测定法,我们表明极性清除是一个活跃的过程,需要TPXL-1激活Aurora A激酶。 TPXL-1集中在与后期极性清除同时发生的星状微管上,其募集Aurora A和激活其激酶活性的能力对于清除至关重要。总而言之,我们的数据将Aurora A激酶鉴定为基于aster的抑制信号,该信号在胞质分裂过程中将收缩环成分限制在细胞赤道内。

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