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The structure of the endoribonuclease XendoU: From small nucleolar RNA processing to severe acute respiratory syndrome coronavirus replication

机译:内切核糖核酸酶XendoU的结构:从小核仁RNA加工到严重的急性呼吸综合征冠状病毒复制

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摘要

Small nucleolar RNAs (snoRNAs) play a key role in eukaryotic ribosome biogenesis. In most cases, snoRNAs are encoded in introns and are released through the splicing reaction. Some snoRNAs are, instead, produced by an alternative pathway consisting of endonucleolytic processing of pre-mRNA. XendoU, the encloribonuclease responsible for this activity, is a U-specific, metal-dependent enzyme that releases products with 2'-3' cyclic phosphate termini. XendoU is broadly conserved among eukaryotes, and it is a genetic marker of nidoviruses, including the severe acute respiratory syndrome coronavirus, where it is essential for replication and transcription. We have determined by crystallography the structure of XendoU that, by refined search methodologies, appears to display a unique fold. Based on sequence conservation, mutagenesis, and docking simulations, we have identified the active site. The conserved structural determinants of this site may provide a framework for attempting to design antiviral drugs to interfere with the infectious nidovirus life cycle.
机译:小核仁RNA(snoRNA)在真核生物核糖体的生物发生中起关键作用。在大多数情况下,snoRNA在内含子中编码,并通过剪接反应释放。相反,某些snoRNA是由另一种途径产生的,该途径由前mRNA的核酸内切加工组成。 XendoU是负责这种活性的环糖核酸酶,是一种U特异性,金属依赖性的酶,可释放带有2'-3'环状磷酸酯末端的产物。 XendoU在真核生物中被广泛保存,它是尼多病毒的遗传标记,包括严重的急性呼吸系统综合症冠状病毒,在其中它对于复制和转录至关重要。我们已经通过晶体学确定了XendoU的结构,通过精细的搜索方法,该结构似乎显示出独特的折叠。基于序列保守,诱变和对接模拟,我们确定了活性位点。该位点的保守结构决定簇可以为尝试设计抗病毒药物以干扰感染性尼多病毒的生命周期提供一个框架。

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