Renzi Fabiana, Caffarelli Elisa, Laneve Pietro, Bozzoni Irene, Brunori Maurizio, Vallone Beatrice
Istituto di Biologia e Patologia Molecolari del Consiglio Nazionale delle Ricerche, 00185 Rome, Italy.
Proc Natl Acad Sci U S A. 2006 Aug 15;103(33):12365-70. doi: 10.1073/pnas.0602426103. Epub 2006 Aug 8.
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 endoribonuclease 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.
小核仁RNA(snoRNAs)在真核生物核糖体生物合成中起关键作用。在大多数情况下,snoRNAs编码于内含子中,并通过剪接反应释放。相反,一些snoRNAs是通过由前体mRNA的内切核酸酶加工组成的替代途径产生的。负责此活性的核糖核酸内切酶XendoU是一种U特异性、金属依赖性酶,它释放具有2'-3'环磷酸末端的产物。XendoU在真核生物中广泛保守,并且是包括严重急性呼吸综合征冠状病毒在内的尼多病毒的遗传标记,在尼多病毒中它对于复制和转录至关重要。我们通过晶体学确定了XendoU的结构,通过精细的搜索方法,该结构似乎呈现出独特的折叠。基于序列保守性、诱变和对接模拟,我们确定了活性位点。该位点保守的结构决定因素可能为尝试设计抗病毒药物以干扰传染性尼多病毒生命周期提供一个框架。