MOE Key Laboratory for Membraneless Organelles and Cellular Dynamics and CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China School of Life Science, Hefei, China; Anhui Key Laboratory for Cellular Dynamics & Chemical Biology, Hefei National Center for Physical Sciences at Nanoscale, Hefei, China; Keck Center for Cellular Dynamics and Organoids Plasticity, Morehouse School of Medicine, Atlanta, Georgia, USA.
MOE Key Laboratory for Membraneless Organelles and Cellular Dynamics and CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China School of Life Science, Hefei, China; Anhui Key Laboratory for Cellular Dynamics & Chemical Biology, Hefei National Center for Physical Sciences at Nanoscale, Hefei, China.
J Biol Chem. 2020 Sep 25;295(39):13419-13431. doi: 10.1074/jbc.REV120.011746. Epub 2020 Jul 22.
Liquid-liquid phase separation (LLPS) of biomolecules drives the formation of subcellular compartments with distinct physicochemical properties. These compartments, free of lipid bilayers and therefore called membraneless organelles, include nucleoli, centrosomes, heterochromatin, and centromeres. These have emerged as a new paradigm to account for subcellular organization and cell fate decisions. Here we summarize recent studies linking LLPS to mitotic spindle, heterochromatin, and centromere assembly and their plasticity controls in the context of the cell division cycle, highlighting a functional role for phase behavior and material properties of proteins assembled onto heterochromatin, centromeres, and central spindles via LLPS. The techniques and tools for visualizing and harnessing membraneless organelle dynamics and plasticity in mitosis are also discussed, as is the potential for these discoveries to promote new research directions for investigating chromosome dynamics, plasticity, and interchromosome interactions in the decision-making process during mitosis.
液-液相分离 (LLPS) 驱动生物分子形成具有不同物理化学性质的亚细胞隔室。这些隔室没有脂双层,因此被称为无膜细胞器,包括核仁、中心体、异染色质和着丝粒。这些隔室已经成为解释亚细胞组织和细胞命运决定的新范例。在这里,我们总结了最近的研究,将液-液相分离与有丝分裂纺锤体、异染色质和着丝粒组装联系起来,并强调了通过液-液相分离组装到异染色质、着丝粒和中心纺锤体上的蛋白质的相行为和物质性质的功能作用。还讨论了用于可视化和利用有丝分裂中无膜细胞器动力学和可塑性的技术和工具,以及这些发现可能为研究染色体动力学、可塑性以及有丝分裂过程中的染色体间相互作用提供新的研究方向。