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1
Ran pathway-independent regulation of mitotic Golgi disassembly by Importin-α.Ran 途径非依赖性调控有丝分裂期高尔基复合体的解体通过 Importin-α。
Nat Commun. 2019 Sep 20;10(1):4307. doi: 10.1038/s41467-019-12207-4.
2
Molecular Mechanism of Cytokinesis.细胞分裂的分子机制。
Annu Rev Biochem. 2019 Jun 20;88:661-689. doi: 10.1146/annurev-biochem-062917-012530. Epub 2019 Jan 16.
3
Importin α Partitioning to the Plasma Membrane Regulates Intracellular Scaling.核输入蛋白α(Importin α)向质膜的分配调节细胞内尺度。
Cell. 2019 Feb 7;176(4):805-815.e8. doi: 10.1016/j.cell.2018.12.001. Epub 2019 Jan 10.
4
RanBP1 Couples Nuclear Export and Golgi Regulation through LKB1 to Promote Cortical Neuron Polarity.RanBP1 通过 LKB1 介导核输出和高尔基体调节促进皮质神经元极性。
Cell Rep. 2018 Sep 4;24(10):2529-2539.e4. doi: 10.1016/j.celrep.2018.07.107.
5
Importin α: functions as a nuclear transport factor and beyond.importin α:作为核转运因子的功能及其他。
Proc Jpn Acad Ser B Phys Biol Sci. 2018;94(7):259-274. doi: 10.2183/pjab.94.018.
6
Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity.细胞内在和外在机制促进细胞类型特异性胞质分裂的多样性。
Elife. 2018 Jul 20;7:e36204. doi: 10.7554/eLife.36204.
7
F-Actin nucleated on chromosomes coordinates their capture by microtubules in oocyte meiosis.在卵母细胞减数分裂中,F 肌动蛋白在染色体上成核,协调微管捕获染色体。
J Cell Biol. 2018 Aug 6;217(8):2661-2674. doi: 10.1083/jcb.201802080. Epub 2018 Jun 14.
8
TPXL-1 activates Aurora A to clear contractile ring components from the polar cortex during cytokinesis.TPXL-1 通过激活 Aurora A,在胞质分裂过程中从极性皮层中清除收缩环成分。
J Cell Biol. 2018 Mar 5;217(3):837-848. doi: 10.1083/jcb.201706021. Epub 2018 Jan 8.
9
Regulation of mitotic spindle assembly factor NuMA by Importin-β.输入蛋白-β对有丝分裂纺锤体组装因子NuMA的调控
J Cell Biol. 2017 Nov 6;216(11):3453-3462. doi: 10.1083/jcb.201705168. Epub 2017 Sep 22.
10
Active Ran regulates anillin function during cytokinesis.在细胞分裂过程中,活性Rho相关蛋白(Ran)调节膜收缩蛋白功能。
Mol Biol Cell. 2017 Nov 15;28(24):3517-3531. doi: 10.1091/mbc.E17-04-0253. Epub 2017 Sep 20.

在有丝分裂过程中 Ran 梯度的补充功能。

Complementary functions for the Ran gradient during division.

机构信息

Department of Biology, Concordia University, Montreal, QC, Canada.

出版信息

Small GTPases. 2021 May;12(3):177-187. doi: 10.1080/21541248.2020.1725371. Epub 2020 Feb 14.

DOI:10.1080/21541248.2020.1725371
PMID:32013678
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7939557/
Abstract

The Ran pathway has a well-described function in nucleocytoplasmic transport, where active Ran dissociates importin/karyopherin-bound cargo containing a nuclear localization signal (NLS) in the nucleus. As cells enter mitosis, the nuclear envelope breaks down and a gradient of active Ran forms where levels are highest near chromatin. This gradient plays a crucial role in regulating mitotic spindle assembly, where active Ran binds to and releases importins from NLS-containing spindle assembly factors. An emerging theme is that the Ran gradient also regulates the actomyosin cortex for processes including polar body extrusion during meiosis, and cytokinesis. For these events, active Ran could play an inhibitory role, where importin-binding may help promote or stabilize a conformation or interaction that favours the recruitment and function of cortical regulators. For either spindle assembly or cortical polarity, the gradient of active Ran determines the extent of importin-binding, the effects of which could vary for different proteins.

摘要

Ran 通路在核质转运中具有明确的功能,其中活跃的 Ran 会从含有核定位信号(NLS)的货物中解离出输入蛋白/核转运蛋白结合物,该货物位于细胞核内。当细胞进入有丝分裂时,核膜会破裂,Ran 会形成一个活跃的梯度,在靠近染色质的地方浓度最高。这个梯度在调节有丝分裂纺锤体组装中起着至关重要的作用,其中活跃的 Ran 会与含有 NLS 的纺锤体组装因子的输入蛋白结合,并将其释放。一个新出现的主题是,Ran 梯度还调节着肌动球蛋白皮层,以促进减数分裂中极体的挤出和胞质分裂等过程。对于这些事件,活跃的 Ran 可能发挥抑制作用,输入蛋白的结合可能有助于促进或稳定一种有利于皮层调节因子募集和功能的构象或相互作用。对于纺锤体组装或皮层极性,活跃的 Ran 梯度决定了输入蛋白结合的程度,这对不同的蛋白质可能会产生不同的影响。