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High-resolution three-dimensional mapping of mRNA export through the nuclear pore

机译:通过核孔的mRNA输出的高分辨率三维映射

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摘要

The flow of genetic information is regulated by selective nucleocytoplasmic transport of messenger RNA:protein complexes (mRNPs) through the nuclear pore complexes (NPCs) of eukaryotic cells. However, the three-dimensional (3D) pathway taken by mRNPs as they transit through the NPC, and the kinetics and selectivity of transport, remain obscure. Here we employ single-molecule fluorescence microscopy with an unprecedented spatiotemporal accuracy of 8?nm and 2?ms to provide new insights into the mechanism of nuclear mRNP export in live human cells. We find that mRNPs exiting the nucleus are decelerated and selected at the centre of the NPC, and adopt a fast-slow-fast diffusion pattern during their brief, ~12?ms, interaction with the NPC. A 3D reconstruction of the export route indicates that mRNPs primarily interact with the periphery on the nucleoplasmic side and in the centre of the NPC, without entering the central axial conduit utilized for passive diffusion of small molecules, and eventually dissociate on the cytoplasmic side.
机译:信使RNA:蛋白质复合物(mRNPs)通过真核细胞的核孔复合物(NPC)的选择性核质运输调节了遗传信息的流动。但是,mRNP通过NPC时所采用的三维(3D)途径以及运输的动力学和选择性仍然不清楚。在这里,我们采用具有空前的时空精度8?nm和2?ms的单分子荧光显微镜技术,为活体人类细胞中核mRNP出口机制提供了新见解。我们发现,离开核的mRNP被减速并选择在NPC的中心,并且在它们与NPC短暂的〜12毫秒相互作用期间采用了快慢速扩散模式。输出路径的3D重建表明,mRNPs主要与核仁一侧和NPC中心的外围相互作用,而没有进入用于小分子被动扩散的中央轴向导管,并最终在胞质一侧解离。

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