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Mechanisms of nuclear pore complex assembly – two different ways of building one molecular machine

机译:核孔复合体组装的机制–构建分子机器的两种不同方法

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摘要

The nuclear pore complex (NPC) mediates all macromolecular transport across the nuclear envelope. In higher eukaryotes that have an open mitosis, NPCs assemble at two points in the cell cycle: during nuclear assembly in late mitosis and during nuclear growth in interphase. How the NPC, the largest nonpolymeric protein complex in eukaryotic cells, self‐assembles inside cells remained unclear. Recent studies have started to uncover the assembly process, and evidence has been accumulating that postmitotic and interphase NPC assembly use fundamentally different mechanisms; the duration, structural intermediates, and regulation by molecular players are different and different types of membrane deformation are involved. In this Review, we summarize the current understanding of these two modes of NPC assembly and discuss the structural and regulatory steps that might drive the assembly processes. We furthermore integrate understanding of NPC assembly with the mechanisms for rapid nuclear growth in embryos and, finally, speculate on the evolutionary origin of the NPC implied by the presence of two distinct assembly mechanisms.
机译:核孔复合体(NPC)介导所有穿过核膜的大分子运输。在具有开放有丝分裂的高级真核生物中,NPC在细胞周期的两个点组装:有丝分裂后期的核组装过程和间期的核生长过程。 NPC是真核细胞中最大的非聚合蛋白复合物,如何在细胞内部自组装尚不清楚。最近的研究已经开始揭示组装过程,并且有证据表明有丝分裂后和相间NPC组装使用根本不同的机制。持续时间,结构中间体和分子参与者的调控是不同的,并且涉及不同类型的膜变形。在这篇评论中,我们总结了对NPC组装这两种模式的当前理解,并讨论了可能推动组装过程的结构和法规步骤。我们进一步将对NPC组装的理解与胚胎中快速核生长的机制结合起来,最后推测存在两种不同组装机制所隐含的NPC的进化起源。

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