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在有丝分裂期间,出芽酵母中的Polo样激酶定位于中心体的不同群体。

The budding yeast Polo-like kinase localizes to distinct populations at centrosomes during mitosis.

作者信息

Botchkarev Vladimir V, Garabedian Mikael V, Lemos Brenda, Paulissen Eric, Haber James E

机构信息

Rosenstiel Basic Medical Sciences Research Center and Department of Biology, Brandeis University, Waltham, MA 02454.

Rosenstiel Basic Medical Sciences Research Center and Department of Biology, Brandeis University, Waltham, MA 02454

出版信息

Mol Biol Cell. 2017 Apr 15;28(8):1011-1020. doi: 10.1091/mbc.E16-05-0324. Epub 2017 Feb 22.

Abstract

The budding yeast Polo-like kinase Cdc5 is a key regulator of many mitotic events. Cdc5 coordinates its functions spatially and temporally by changing its localization during the cell cycle: Cdc5 is imported into the nucleus in G2 phase and released to the cytoplasm in anaphase, where it accumulates at the bud neck. Cdc5 also localizes to the spindle pole bodies (SPBs) from S phase until the end of mitosis. Whether Cdc5 changes its SPB population during the cell cycle is not known. We find that Cdc5 localizes to distinct SPB subpopulations, depending on the mitotic stage. Cdc5 localizes to the nuclear side of the SPBs during metaphase and early anaphase and to the cytoplasmic surface of the SPBs during late anaphase. Cdc14 is necessary to relocalize Cdc5 from the nuclear SPB plaque. Accumulation of Cdc5 at the daughter SPB in late anaphase is controlled by Bfa1. We also show that Cdc5 and Bfa1 are found in spatially distinct locations at the SPBs during G2/M arrest after DNA damage. Collectively our data reveal that Cdc5 is a dynamic component of the SPBs during mitosis and provide new insight into its regulation during both late mitotic events and DNA damage-induced G2/M arrest.

摘要

出芽酵母中的Polo样激酶Cdc5是许多有丝分裂事件的关键调节因子。Cdc5通过在细胞周期中改变其定位在空间和时间上协调其功能:Cdc5在G2期被导入细胞核,并在后期释放到细胞质中,在那里它聚集在芽颈处。Cdc5也从S期到有丝分裂结束定位于纺锤体极体(SPB)。Cdc5在细胞周期中是否改变其SPB数量尚不清楚。我们发现,根据有丝分裂阶段的不同,Cdc5定位于不同的SPB亚群。在中期和早后期,Cdc5定位于SPB的核侧,而在晚后期定位于SPB的细胞质表面。Cdc14是将Cdc5从核SPB斑块重新定位所必需的。晚后期Cdc5在子SPB处的积累受Bfa1控制。我们还表明,在DNA损伤后的G2/M期停滞期间,Cdc5和Bfa1在SPB的空间位置不同。总体而言,我们的数据表明Cdc5在有丝分裂期间是SPB的动态组成部分,并为其在有丝分裂后期事件和DNA损伤诱导的G2/M期停滞期间的调节提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec9d/5391178/3c659520efd8/1011fig1.jpg

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