Meiotic nuclear pore complex remodeling provides key insights into nuclear basket organization

Grant A. King, Rahel Wettstein, Joseph M. Varberg, Keerthana Chetlapalli, M. E. Walsh, Ludovic C. Gillet, Claudia Hernandez-Armenta, P. Beltrão, R. Aebersold, S. Jaspersen, Joao Matos, E. Ünal
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引用次数: 3

Abstract

Nuclear pore complexes (NPCs) are large proteinaceous assemblies that mediate nuclear compartmentalization. NPCs undergo largescale structural rearrangements during mitosis in metazoans and some fungi. However, our understanding of NPC remodeling beyond mitosis remains limited. Using time-lapse fluorescence microscopy, we discovered that NPCs undergo two mechanistically-separable remodeling events during budding yeast meiosis whereby parts or all of the nuclear basket transiently dissociate from the NPC core during meiosis I and II, respectively. Meiosis I detachment, observed for Nup60 and Nup2, is driven by Polo kinase-mediated phosphorylation of Nup60 at its interface with the Y-complex. Subsequent reattachment of Nup60-Nup2 to the NPC core is mediated by a lipid-binding amphipathic helix in Nup60. Preventing Nup60-Nup2 reattachment causes misorganization of the entire nuclear basket in gametes. Strikingly, meiotic nuclear basket remodeling also occurs in the distantly related fission yeast, Schizosaccharomyces pombe. Our study reveals a conserved and developmentally programmed aspect of NPC plasticity, providing key mechanistic insights into nuclear basket organization. SUMMARY King and Wettstein et al. reveal that nuclear pore complexes undergo two distinct remodeling events during budding yeast meiosis: partial and full nuclear basket detachment. By dissecting the regulation of these events, the study provides mechanistic insights into NPC organization.
减数分裂核孔复合体的重塑为核篮组织提供了关键的见解
核孔复合物(NPCs)是介导核区隔化的大型蛋白质组合物。在后生动物和一些真菌的有丝分裂过程中,npc经历了大规模的结构重排。然而,除了有丝分裂之外,我们对鼻咽癌重塑的理解仍然有限。利用时移荧光显微镜,我们发现在出芽酵母减数分裂期间,NPC经历了两个机械可分离的重塑事件,即部分或全部核篮分别在减数分裂I和II期间短暂地与NPC核心分离。在Nup60和Nup2中观察到的减数分裂I分离是由Polo激酶介导的Nup60与y复合物界面的磷酸化驱动的。随后Nup60- nup2再附着到NPC核心是由Nup60中的脂质结合两亲螺旋介导的。防止Nup60-Nup2再附着会导致配子中整个核篮组织错误。引人注目的是,减数分裂核篮重塑也发生在与分裂酵母有亲缘关系的裂糖酵母中。我们的研究揭示了NPC可塑性的保守和发育程序化方面,为核篮子组织提供了关键的机制见解。King和Wettstein等人发现,在出芽酵母减数分裂过程中,核孔复合物经历了两种不同的重塑事件:核篮部分脱离和核篮完全脱离。通过剖析这些事件的规则,该研究为人大组织提供了机制见解。
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