Malecki Marek, Malecki Bianca
Western University of Health Sciences (WUHS), Pomona, CA, USA.
J Fertili In Vitro. 2012 Apr 30;2012(2):108-118. doi: 10.4172/2165-74.
The molecular architecture of Nuclear Pore Complexes (NPCs), as well as the import and export of molecules through them, has been intensively studied in a variety of cells, including oocytes. However, the structures and mechanisms, involved in the transport of molecules beyond the NPCs, remained unclear, until now. The specific aim of this work was, therefore, to determine, if there exist any intranuclear structures in continuum with the NPCs. This information could help in explaining the mechanisms, which propel the distribution of biomolecules and vectors inside the cell nuclei.To attain this aim, we used rapid cryo-immobilization to capture molecular processes of living cells with millisecond resolution. We pursued molecular imaging, including electron energy loss spectroscopy and energy dispersive x-ray spectroscopy, to reveal structures with nanometer spatial resolution. We also bioengineered single chain variable fragments to track biomolecules and transgenes' constructs.Herein, we reveal the Nuclear Routing Networks (NRNs) in the oocytes of Xenopus laevis. The NRNs originate at and extend from the tops of intranuclear baskets of the NPCs to interconnect them, while creating a complex, intra-nuclear, three-dimensional architecture. The NRNs guide the export of both tRNA, as well as the Nuclear Export Signal (NES) equipped vectors, from the nuclei. Moreover, the NRNs guide the import of both nucleoplasmin, as well as the Nuclear Localization Signals (NLS) modified transgenes' vectors, into the nuclei. The vectors equipped with these NLS and NES shuttle back and forth through the NPCs and NRNs.To summarize, we reveal the NRN, which functions as the guided distribution system in the Xenopus laevis oocytes' nuclei. We further proceed with the identification of its molecular components.
核孔复合体(NPCs)的分子结构,以及分子通过它们的进出,已经在包括卵母细胞在内的多种细胞中得到了深入研究。然而,直到现在,参与NPCs之外分子运输的结构和机制仍不清楚。因此,这项工作的具体目标是确定是否存在与NPCs连续的核内结构。这些信息有助于解释推动生物分子和载体在细胞核内分布的机制。为了实现这一目标,我们使用快速冷冻固定技术以毫秒级分辨率捕获活细胞的分子过程。我们进行了分子成像,包括电子能量损失谱和能量色散X射线谱,以揭示具有纳米空间分辨率的结构。我们还对单链可变片段进行了生物工程改造,以追踪生物分子和转基因构建体。在此,我们揭示了非洲爪蟾卵母细胞中的核转运网络(NRNs)。NRNs起源于NPCs核内篮筐的顶部并从其延伸出来,将它们相互连接,同时形成一个复杂的核内三维结构。NRNs引导tRNA以及配备核输出信号(NES)的载体从细胞核输出。此外,NRNs引导核质蛋白以及经核定位信号(NLS)修饰的转基因载体进入细胞核。配备这些NLS和NES的载体在NPCs和NRNs之间来回穿梭。总之,我们揭示了在非洲爪蟾卵母细胞核中作为引导分布系统发挥作用的NRN。我们进一步着手鉴定其分子成分。