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着丝粒和 Polo 激酶对中心体蛋白的重分配控制了有丝分裂酵母中部分核膜的崩解。

Redistribution of centrosomal proteins by centromeres and Polo kinase controls partial nuclear envelope breakdown in fission yeast.

机构信息

Stowers Institute for Medical Research, Kansas City, MO 64110.

Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160.

出版信息

Mol Biol Cell. 2021 Aug 1;32(16):1487-1500. doi: 10.1091/mbc.E21-05-0239. Epub 2021 Jun 16.

Abstract

Proper mitotic progression in requires partial nuclear envelope breakdown (NEBD) and insertion of the spindle pole body (SPB-yeast centrosome) to build the mitotic spindle. Linkage of the centromere to the SPB is vital to this process, but why that linkage is important is not well understood. Utilizing high-resolution structured illumination microscopy, we show that the conserved Sad1-UNC-84 homology-domain protein Sad1 and other SPB proteins redistribute during mitosis to form a ring complex around SPBs, which is a precursor for localized NEBD and spindle formation. Although the Polo kinase Plo1 is not necessary for Sad1 redistribution, it localizes to the SPB region connected to the centromere, and its activity is vital for redistribution of other SPB ring proteins and for complete NEBD at the SPB to allow for SPB insertion. Our results lead to a model in which centromere linkage to the SPB drives redistribution of Sad1 and Plo1 activation that in turn facilitate partial NEBD and spindle formation through building of a SPB ring structure.

摘要

在有丝分裂过程中,需要部分核膜破裂(NEBD)和纺锤体极体(SPB-酵母中心体)的插入,以构建有丝分裂纺锤体。着丝粒与 SPB 的连接对这个过程至关重要,但为什么这种连接很重要还不是很清楚。利用高分辨率结构照明显微镜,我们发现保守的 Sad1-UNC-84 同源结构域蛋白 Sad1 和其他 SPB 蛋白在有丝分裂期间重新分布,在 SPB 周围形成一个环复合物,这是局部 NEBD 和纺锤体形成的前体。尽管 Polo 激酶 Plo1 对于 Sad1 的重新分布不是必需的,但它定位于与着丝粒相连的 SPB 区域,其活性对于其他 SPB 环蛋白的重新分布以及在 SPB 处完全进行 NEBD 以允许 SPB 插入是至关重要的。我们的结果提出了一个模型,即着丝粒与 SPB 的连接驱动 Sad1 的重新分布和 Plo1 的激活,这反过来又通过构建 SPB 环结构来促进部分 NEBD 和纺锤体的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e868/8351742/663767f2bbb0/mbc-32-1487-g001.jpg

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