a Department of Chromosome Biology; Max F. Perutz Laboratories ; University of Vienna ; Vienna , Austria.
RNA Biol. 2014;11(10):1226-32. doi: 10.4161/15476286.2014.972856.
The double-stranded RNA-binding domain (dsRBD) is a small protein domain found in eukaryotic, prokaryotic and viral proteins, whose central property is to bind to double-stranded RNA (dsRNA). Aside from this major function, recent examples of dsRBDs involved in the regulation of the sub-cellular localization of proteins, suggest that the participation of dsRBDs in nucleocytoplasmic trafficking is likely to represent a widespread auxiliary function of this type of RNA-binding domain. Overall, dsRBDs from proteins involved in many different biological processes have been reported to be implicated in nuclear import and export, as well as cytoplasmic, nuclear and nucleolar retention. Interestingly, the function of dsRBDs in nucleocytoplasmic trafficking is often regulated by their dsRNA-binding capacity, which can either enhance or impair the transport from one compartment to another. Here, we present and discuss the emerging function of dsRBDs in nucleocytoplasmic transport.
双链 RNA 结合域(dsRBD)是一种存在于真核生物、原核生物和病毒蛋白中的小蛋白结构域,其核心特性是结合双链 RNA(dsRNA)。除了这一主要功能外,最近发现 dsRBD 参与蛋白质亚细胞定位的调控,表明 dsRBD 参与核质转运可能代表这种 RNA 结合结构域的一种广泛的辅助功能。总体而言,参与许多不同生物过程的蛋白质中的 dsRBD 已被报道与核输入和输出以及细胞质、核和核仁保留有关。有趣的是,dsRBD 在核质转运中的功能通常受其 dsRNA 结合能力的调节,这种能力可以增强或削弱从一个隔室到另一个隔室的运输。在这里,我们提出并讨论了 dsRBD 在核质转运中的新兴功能。