Department of Biology, Concordia University, Montreal, QC, Canada.
Small GTPases. 2021 May;12(3):177-187. doi: 10.1080/21541248.2020.1725371. Epub 2020 Feb 14.
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.
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。