Rotem Asaf, Gruber Rita, Shorer Hagai, Shaulov Lihi, Klein Eugenia, Harel Amnon
Department of Biology, Technion-Israel Institute of Technology, Haifa 32000, Israel.
Mol Biol Cell. 2009 Sep;20(18):4031-42. doi: 10.1091/mbc.e09-02-0150. Epub 2009 Jul 22.
The nuclear envelope of higher eukaryotic cells reforms at the exit from mitosis, in concert with the assembly of nuclear pore complexes (NPCs). The first step in postmitotic NPC assembly involves the "seeding" of chromatin with ELYS and the Nup107-160 complex. Subsequent steps in the assembly process are poorly understood and different mechanistic models have been proposed to explain the formation of the full supramolecular structure. Here, we show that the initial step of chromatin seeding is negatively regulated by importin beta. Direct imaging of the chromatin attachment sites reveals single sites situated predominantly on the highest substructures of chromatin surface and lacking any sign of annular structures or oligomerized pre-NPCs. Surprisingly, the inhibition by importin beta is only partially reversed by RanGTP. Importin beta forms a high-molecular-weight complex with both ELYS and the Nup107-160 complex in cytosol. We suggest that initiation sites for NPC assembly contain single copies of chromatin-bound ELYS/Nup107-160 and that the lateral oligomerization of these subunits depends on the recruitment of membrane components. We predict that additional regulators, besides importin beta and Ran, may be involved in coordinating the initial seeding of chromatin with subsequent steps in the NPC assembly pathway.
高等真核细胞的核膜在有丝分裂退出时重新形成,与核孔复合体(NPC)的组装同步进行。有丝分裂后NPC组装的第一步涉及用ELYS和Nup107 - 160复合体对染色质进行“播种”。组装过程中的后续步骤了解甚少,并且已经提出了不同的机制模型来解释完整超分子结构的形成。在这里,我们表明染色质播种的初始步骤受到输入蛋白β的负调控。对染色质附着位点的直接成像显示,单个位点主要位于染色质表面的最高亚结构上,并且没有任何环形结构或寡聚化前体NPC的迹象。令人惊讶的是,输入蛋白β的抑制作用仅被RanGTP部分逆转。输入蛋白β在细胞质中与ELYS和Nup107 - 160复合体形成高分子量复合物。我们认为NPC组装的起始位点包含与染色质结合的ELYS/Nup107 - 160的单拷贝,并且这些亚基的侧向寡聚化取决于膜成分的募集。我们预测,除了输入蛋白β和Ran之外,其他调节因子可能参与协调染色质的初始播种与NPC组装途径中的后续步骤。