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Transport of messenger RNA from the nucleus to the cytoplasm.

机译:信使RNA从细胞核到细胞质的转运。

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摘要

All movement of molecules and macromolecules between the cytoplasm and the nucleus takes place through nuclear pore complexes (NPCs), very large macromolecular complexes that are the only channels connecting these compartments. mRNA export is mediated by multiple, highly conserved protein factors that couple steps of nuclear pre-mRNA biogenesis to mRNA transport. Mature messenger ribonucleoproteins (mRNPs) diffuse from sites of transcription to NPCs, although some active genes are positioned at the nuclear periphery where they interact physically with components of NPCs. As properly processed mRNPs translocate through the pore, certain mRNP proteins are removed, probably through the enzymatic action of the DEAD-box helicase Dbp5, which binds to Nup159 and Gle1, components of the cytoplasmic filaments of the NPC. Gle1 and the phosphoinositide IP6 activate Dbp5's ATPase activity in vitro and this could provide critical spatial regulation of Dbp5 activity in vivo.
机译:分子和大分子在细胞质和细胞核之间的所有运动都是通过核孔复合物(NPC)进行的,核孔复合物是非常大的大分子复合物,是连接这些部分的唯一通道。 mRNA的输出是由多种高度保守的蛋白质因子介导的,这些因子将核前mRNA生物发生的步骤与mRNA的运输相结合。成熟的信使核糖核蛋白(mRNPs)从转录位点扩散到NPC,尽管一些活性基因位于核外围,与NPC的成分发生物理相互作用。当正确加工的mRNPs通过孔移位时,某些mRNP蛋白可能会被DEAD-box解旋酶Dbp5的酶促作用去除,该酶与NPC胞质丝的成分Nup159和Gle1结合。 Gle1和磷酸肌醇IP6在体外激活Dbp5的ATPase活性,这可以在体内为Dbp5活性提供关键的空间调节。

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