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Regulation of mRNA Trafficking by Nuclear Pore Complexes

机译:核孔复合体对mRNA贩运的调节

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摘要

Over the last two decades, multiple studies have explored the mechanisms governing mRNA export out of the nucleus, a crucial step in eukaryotic gene expression. During transcription and processing, mRNAs are assembled into messenger ribonucleoparticles (mRNPs). mRNPs are then exported through nuclear pore complexes (NPCs), which are large multiprotein assemblies made of several copies of a limited number of nucleoporins. A considerable effort has been put into the dissection of mRNA export through NPCs at both cellular and molecular levels, revealing the conserved contributions of a subset of nucleoporins in this process, from yeast to vertebrates. Several reports have also demonstrated the ability of NPCs to sort out properly-processed mRNPs for entry into the nuclear export pathway. Importantly, changes in mRNA export have been associated with post-translational modifications of nucleoporins or changes in NPC composition, depending on cell cycle progression, development or exposure to stress. How NPC modifications also impact on cellular mRNA export in disease situations, notably upon viral infection, is discussed.
机译:在过去的二十年中,多项研究探索了控制mRNA从核中输出的机制,这是真核基因表达的关键步骤。在转录和加工过程中,mRNA组装成信使核糖核酸颗粒(mRNPs)。然后,mRNP通过核孔复合物(NPC)输出,核孔复合物是由有限数量的核孔蛋白的多个副本组成的大型多蛋白组件。人们已经在细胞和分子水平上对通过NPC进行mRNA出口的解剖进行了相当大的努力,从而揭示了从酵母菌到脊椎动物在此过程中一部分核孔蛋白的保守贡献。几份报告还表明,全国人大有能力挑选出经过适当处理的mRNP,以进入核出口途径。重要的是,取决于细胞周期进程,发育或暴露于压力下,mRNA输出的变化与核孔蛋白的翻译后修饰或NPC组成的变化有关。讨论了在疾病情况下,特别是在病毒感染时,NPC修饰如何也影响细胞mRNA的输出。

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