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着丝粒结合因子3(CBF3)在纺锤体稳定性、胞质分裂和动粒附着中的作用。

The role of centromere-binding factor 3 (CBF3) in spindle stability, cytokinesis, and kinetochore attachment.

作者信息

Bouck David, Bloom Kerry

机构信息

Department of Cell Biology, University of North Carolina, Durham, NC 27599, USA.

出版信息

Biochem Cell Biol. 2005 Dec;83(6):696-702. doi: 10.1139/o05-161.

Abstract

The spindle midzone is critical for spindle stability and cytokinesis. Chromosomal passenger proteins relocalize from chromosomes to the spindle midzone after anaphase onset. The recent localization of the inner-kinetochore, centromere-binding factor 3 (CBF3) complex to the spindle midzone in budding yeast has led to the discovery of novel functions for this complex in addition to its essential role at kinetochores. In G1/S cells, CBF3 components are detected along dynamic microtubules, where they can "search-and-capture" newly replicated centromeres. During anaphase, CBF3 is transported to the microtubule plus-ends of the spindle midzone. Consistent with this localization, cells containing a mutation in the CBF3 subunit Ndc10p show defects in spindle stability during anaphase. In addition, ndc10-1 cells show defects during cytokinesis, resulting in a defect in cell abscission. These results highlight the importance of midzone-targeted proteins in coordinating mitosis with cell division. Here we discuss these findings and explore the significance of CBF3 transport to microtubule plus-ends at the spindle midzone.

摘要

纺锤体中区对于纺锤体稳定性和胞质分裂至关重要。后期开始后,染色体乘客蛋白从染色体重新定位到纺锤体中区。芽殖酵母中内着丝粒、着丝粒结合因子3(CBF3)复合体最近定位于纺锤体中区,这导致发现该复合体除了在着丝粒发挥关键作用外还具有新功能。在G1/S期细胞中,可沿着动态微管检测到CBF3组分,它们在微管上可“搜索并捕获”新复制的着丝粒。在后期,CBF3被转运到纺锤体中区的微管正端。与这种定位一致,CBF3亚基Ndc10p发生突变的细胞在后期纺锤体稳定性方面表现出缺陷。此外,ndc10 - 1细胞在胞质分裂期间表现出缺陷,导致细胞脱离缺陷。这些结果突出了中区靶向蛋白在协调有丝分裂与细胞分裂中的重要性。在此我们讨论这些发现,并探讨CBF3转运到纺锤体中区微管正端的意义。

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