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高尔基分割控制着有丝分裂的进入通过 Aurora-A 激酶。

Golgi partitioning controls mitotic entry through Aurora-A kinase.

机构信息

Department of Cell Biology and Oncology, Consorzio Mario Negri Sud, 66030 Santa Maria Imbaro, Chieti, Italy.

出版信息

Mol Biol Cell. 2010 Nov 1;21(21):3708-21. doi: 10.1091/mbc.E10-03-0243. Epub 2010 Sep 15.

Abstract

At the onset of mitosis, the Golgi complex undergoes a multistep fragmentation process that is required for its correct partitioning into the daughter cells. Inhibition of this Golgi fragmentation results in cell cycle arrest at the G2 stage, suggesting that correct inheritance of the Golgi complex is monitored by a "Golgi mitotic checkpoint." However, the molecular basis of this G2 block is not known. Here, we show that the G2-specific Golgi fragmentation stage is concomitant with centrosome recruitment and activation of the mitotic kinase Aurora-A, an essential regulator for entry into mitosis. We show that a block of Golgi partitioning impairs centrosome recruitment and activation of Aurora-A, which results in the G2 block of cell cycle progression. Overexpression of Aurora-A overrides this cell cycle block, indicating that Aurora-A is a major effector of the Golgi checkpoint. Our findings provide the basis for further understanding of the signaling pathways that coordinate organelle inheritance and cell duplication.

摘要

有丝分裂开始时,高尔基体经历一个多步骤的碎片化过程,这是高尔基体正确分配到子细胞所必需的。抑制这种高尔基体碎片化会导致细胞在 G2 期停滞,这表明高尔基体的正确遗传是由一个“高尔基体有丝分裂检查点”来监测的。然而,这种 G2 阻断的分子基础尚不清楚。在这里,我们表明,G2 特异性的高尔基体碎片化阶段与中心体的募集和有丝分裂激酶 Aurora-A 的激活同时发生,Aurora-A 是进入有丝分裂的必需调节剂。我们表明,高尔基体分裂的阻断会损害中心体的募集和 Aurora-A 的激活,从而导致细胞周期进程的 G2 阻断。Aurora-A 的过表达可以克服这个细胞周期阻断,表明 Aurora-A 是高尔基体检查点的主要效应因子。我们的发现为进一步理解协调细胞器遗传和细胞复制的信号通路提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcb9/2965687/0c1b924bd12d/zmk0211096310002.jpg

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