The Mina & Everard Goodman Faculty of Life Sciences & Institute of Nanotechnology, Bar-Ilan University, Ramat Gan 52900, Israel.
Nat Cell Biol. 2010 Jun;12(6):543-52. doi: 10.1038/ncb2056. Epub 2010 May 9.
The flow of genetic information in eukaryotic cells occurs through the nucleocytoplasmic translocation of mRNAs. Knowledge of in vivo messenger RNA export kinetics remains poor in comparison with that of protein transport. We have established a mammalian system that allowed the real-time visualization and quantification of large single mRNA-protein complexes (mRNPs) during export. The in vivo dynamics of bulk mRNP transport and export, from transcription to the nuclear pore complex (NPC), occurred within a 5-40 minute time frame, with no NPC pile-up. mRNP export was rapid (about 0.5 s) and kinetically faster than nucleoplasmic diffusion. Export inhibition demonstrated that mRNA-NPC interactions were independent of ongoing export. Nucleoplasmic transport dynamics of intron-containing and intronless mRNAs were similar, yet an intron did increase export efficiency. Here we provide visualization and analysis at the single mRNP level of the various steps in nuclear gene expression and the inter-chromatin tracks through which mRNPs diffuse, and demonstrate the kinetics of mRNP-NPC interactions and translocation.
真核细胞中的遗传信息流动是通过 mRNA 的核质转运来实现的。与蛋白质转运相比,人们对体内信使 RNA 输出动力学的了解仍然很差。我们建立了一种哺乳动物系统,允许在出口过程中实时可视化和定量大型单个 mRNA-蛋白质复合物(mRNP)。从转录到核孔复合物(NPC)的大量 mRNP 运输和输出的体内动力学在 5-40 分钟的时间范围内发生,没有 NPC 堆积。mRNP 出口速度很快(约 0.5 秒),在动力学上快于核质扩散。出口抑制表明 mRNA-NPC 相互作用独立于正在进行的出口。含有内含子和不含内含子的 mRNA 的核质运输动力学相似,但内含子确实提高了出口效率。在这里,我们在单个 mRNP 水平上提供了核基因表达各个步骤的可视化和分析,以及 mRNP 在染色质间扩散的轨迹,并证明了 mRNP-NPC 相互作用和易位的动力学。