Centre for Cancer Biomedicine, Faculty of Medicine, University of Oslo, Montebello, 0379 Oslo, Norway; Department of Molecular Cell Biology, Institute for Cancer Research, Oslo University Hospital, Montebello, 0379 Oslo, Norway.
Centre for Cancer Biomedicine, Faculty of Medicine, University of Oslo, Montebello, 0379 Oslo, Norway; Department of Molecular Cell Biology, Institute for Cancer Research, Oslo University Hospital, Montebello, 0379 Oslo, Norway; Centre of Molecular Inflammation Research, Norwegian University of Science and Technology, Faculty of Medicine, 7491 Trondheim, Norway.
Trends Cell Biol. 2017 Jan;27(1):1-11. doi: 10.1016/j.tcb.2016.10.001. Epub 2016 Oct 31.
Cytokinesis is the final stage of cell division and is concluded by abscission of the intercellular bridge to physically separate the daughter cells. Timing of cytokinetic abscission is monitored by a molecular machinery termed the abscission checkpoint. This machinery delays abscission in cells with persistent chromatin in the intercellular bridge. Recent work has also uncovered its response to high membrane tension, nuclear pore defects, and DNA replication stress. Although it is known that the abscission checkpoint depends on persistent activity of the Aurora B protein kinase, we have only recently begun to understand its molecular basis. We propose here a molecular framework for abscission checkpoint signaling and we discuss outstanding questions relating to its function and physiological relevance.
胞质分裂是细胞分裂的最后阶段,通过细胞间桥的断裂将子细胞物理分离来完成。胞质分裂的时间由一个称为胞质分裂检查点的分子机制来监测。这个机制会延迟在细胞间桥中持续存在染色质的细胞的胞质分裂。最近的研究还揭示了它对高膜张力、核孔缺陷和 DNA 复制应激的反应。尽管人们已经知道胞质分裂检查点依赖于 Aurora B 蛋白激酶的持续活性,但我们直到最近才开始了解其分子基础。我们在这里提出了一个胞质分裂检查点信号的分子框架,并讨论了与其功能和生理相关性相关的未解决问题。