核蛋白转运途径。

M Köhler, H Haller, E Hartmann
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引用次数: 32

摘要

像转录因子和核糖体蛋白这样的核蛋白是在细胞质中合成的,必须被运送到细胞核中才能完成它们的功能。>20- 60kd的蛋白质通过核孔复合物(NPC)进入细胞核是一个主动的、需要能量的过程。转运底物被转运蛋白通过一定的信号识别。最具特征的蛋白质输入途径是“经典的”核定位信号依赖途径,其输入蛋白α和β将底物携带到NPC。进口蛋白-底物复合物进入细胞核的运输是由小GTPase Ran/TC4调控的。在过去的几年里,已经发现了十多种蛋白质,这些蛋白质已经被证明或很可能是具有不同进口途径的核转运因子:进口蛋白α家族的成员非常相似,并且与进口蛋白β核定位信号携带蛋白复杂地转运到细胞核中。ran结合蛋白家族的成员与输入β蛋白有微弱的相似性。它们在氨基端有一个共同的结构域,能够结合RanGTP,这是它们作为不同蛋白质或rna的核输入或输出因子功能的先决条件。然而,Ran/TC4似乎在迄今所描述的所有核转运途径中起着关键的调节作用,尽管通过NPC的转运步骤的分子机制尚不清楚。
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Nuclear protein transport pathways.

Nuclear proteins like transcription factors and ribosomal proteins are synthesized in the cytoplasm and have to be transported into the nucleus to fulfill their functions. The transport of proteins >20-60 kD through the nuclear pore complex (NPC) into the nucleus is an active, energy-requiring process. Transport substrates are recognized by their transport proteins via certain signals. The best-characterized protein import pathway is the 'classical' nuclear localization signal-dependent pathway with importin alpha and beta carrying the substrate to the NPC. The transport of the importin-substrate complex into the nucleus is regulated by the small GTPase Ran/TC4. During the last years more than ten proteins have been discovered which have already been proven or are very likely to be nuclear transport factors of distinct import pathways: members of the importin alpha protein family are very similar and transport in complex with importin beta nuclear localization signal-bearing proteins into the nucleus. Members of the Ran-binding protein family show some weak similarity to importin beta. Sharing a common domain at the amino terminus, they are able to bind RanGTP, a prerequisite for their function as nuclear import or export factors for distinct proteins or RNAs. However, Ran/TC4 seems to play a key regulatory role in all nuclear transport pathways described so far, although the molecular mechanism of the translocation step through the NPC is still unclear.

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