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本文引用的文献

1
Nuclear body phase separation drives telomere clustering in ALT cancer cells.核体相分离驱动端粒在端粒延长替代途径(ALT)癌细胞中聚集。
Mol Biol Cell. 2020 Aug 15;31(18):2048-2056. doi: 10.1091/mbc.E19-10-0589. Epub 2020 Jun 24.
2
Crowning the Kinetochore: The Fibrous Corona in Chromosome Segregation.着丝粒之冕:染色体分离中的纤维冠
Trends Cell Biol. 2020 Aug;30(8):653-667. doi: 10.1016/j.tcb.2020.04.006. Epub 2020 May 5.
3
SARS-CoV-2 productively infects human gut enterocytes.SARS-CoV-2 能有效地感染人类肠道肠细胞。
Science. 2020 Jul 3;369(6499):50-54. doi: 10.1126/science.abc1669. Epub 2020 May 1.
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Mechanisms generating cancer genome complexity from a single cell division error.从单个细胞分裂错误中产生癌症基因组复杂性的机制。
Science. 2020 Apr 17;368(6488). doi: 10.1126/science.aba0712.
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Mps1 dimerization and multisite interactions with Ndc80 complex enable responsive spindle assembly checkpoint signaling.Mps1 二聚化和与 Ndc80 复合物的多部位相互作用使纺锤体组装检查点信号具有响应性。
J Mol Cell Biol. 2020 Jul 1;12(7):486-498. doi: 10.1093/jmcb/mjaa006.
6
Cyclin B1 scaffolds MAD1 at the kinetochore corona to activate the mitotic checkpoint.周期蛋白 B1 将 MAD1 支架在着丝粒冠上以激活有丝分裂检查点。
EMBO J. 2020 Jun 17;39(12):e103180. doi: 10.15252/embj.2019103180. Epub 2020 Mar 23.
7
Physical Principles Underlying the Complex Biology of Intracellular Phase Transitions.细胞内相转变的复杂生物学的物理原理。
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TTK inhibition radiosensitizes basal-like breast cancer through impaired homologous recombination.TTK 抑制通过损伤同源重组增强基底样乳腺癌的放射敏感性。
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Dev Cell. 2020 Feb 10;52(3):277-293.e8. doi: 10.1016/j.devcel.2019.11.019. Epub 2019 Dec 19.
10
Mechanosensation of Tight Junctions Depends on ZO-1 Phase Separation and Flow.机械感知紧密连接取决于 ZO-1 的相分离和流动。
Cell. 2019 Oct 31;179(4):937-952.e18. doi: 10.1016/j.cell.2019.10.006.

相分离驱动细胞分裂中的决策。

Phase separation drives decision making in cell division.

机构信息

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.

出版信息

J Biol Chem. 2020 Sep 25;295(39):13419-13431. doi: 10.1074/jbc.REV120.011746. Epub 2020 Jul 22.

DOI:10.1074/jbc.REV120.011746
PMID:32699013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7521646/
Abstract

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.

摘要

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。