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RNA recognition by double-stranded RNA binding domains: a matter of shape and sequence

机译:RNa识别由双链RNa结合结构域:形状和序列的一个问题

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摘要

The double stranded RNA binding domain (dsRBD) is a small protein domain of 65–70 amino acids adopting an αβββα fold, whose central property is to bind to double stranded RNA (dsRNA). This domain is present in proteins implicated in many aspects of cellular life, including antiviral response, RNA editing, RNA processing, RNA transport and last but not least RNA silencing. Even though proteins containing dsRBDs can bind to very specific dsRNA targets in vivo, the binding of dsRBDs to dsRNA is commonly believed to be shape-dependent rather than sequence-specific. Interestingly, recent structural information on dsRNA recognition by dsRBDs opens the possibility that this domain performs a direct readout of RNA sequence in the minor groove, allowing a global reconsideration of the principles describing dsRNA recognition by dsRBDs. We review in this article the current structural and molecular knowledge on dsRBDs emphasizing the intricate relationship between the amino acid sequence, the structure of the domain and its RNA recognition capacity. We especially focus on the molecular determinants of dsRNA recognition and describe how sequence discrimination can be achieved by this type of domain.
机译:双链RNA结合结构域(dsRBD)是65-70个氨基酸的小蛋白结构域,具有αβββα折叠,其中心特性是与双链RNA(dsRNA)结合。该结构域存在于涉及细胞生命许多方面的蛋白质中,包括抗病毒反应,RNA编辑,RNA加工,RNA转运以及最后但并非最不重要的RNA沉默。即使含有dsRBD的蛋白质可以在体内与非常特定的dsRNA靶标结合,但通常认为dsRBD与dsRNA的结合是形状依赖性的,而不是序列特异性的。有趣的是,有关dsRBD识别dsRNA的最新结构信息打开了该域在小沟中直接读出RNA序列的可能性,从而使人们重新考虑了dsRBD识别dsRNA的原理。我们在本文中回顾了有关dsRBD的当前结构和分子知识,强调了氨基酸序列,结构域结构及其RNA识别能力之间的复杂关系。我们特别关注dsRNA识别的分子决定因素,并描述如何通过这种类型的结构域实现序列区分。

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