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The common and the distinctive features of the bulged-G motif based on a 1.04 A resolution RNA structure

机译:基于1.04 A分辨率RNA结构的凸出G基序的共有特征

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Bulged-G motifs are ubiquitous internal RNA loops that provide specific recognition sites for proteins and RNAs. To establish the common and distinctive features of the motif we determined the structures of three variants and compared them with related structures. The variants are 27-nt mimics of the sarcin/ricin loop (SRL) from Escherichia coli 23S ribosomal RNA that is an essential part of the binding site for elongation factors (EFs). The wild-type SRL has now been determined at 1.04 A resolution, supplementing data obtained before at 1.11 A and allowing the first calculation of coordinate error for an RNA motif. The other two structures, having a viable (C2658U·G2663A) or a lethal mutation (C2658G· G2663C), were determined at 1.75 and 2.25 A resolution, respectively. Comparisons reveal that bulged-G motifs have a common hydration and geometry, with flexible junctions at flanking structural elements. Six conserved nucleotides preserve the fold of the motif; the remaining seven to nine vary in sequence and alter contacts in both grooves. Differences between accessible functional groups of the lethal mutation and those of the viable mutation and wild-type SRL may account for the impaired elongation factor binding to ribosomes with the C2658G?G2663C mutation and may underlie the lethal phenotype.
机译:凸起的G基序是普遍存在的内部RNA环,可为蛋白质和RNA提供特定的识别位点。为了确定主题的共有特征,我们确定了三种变体的结构,并将它们与相关结构进行了比较。这些变体是来自大肠杆菌23S核糖体RNA的sarcin / ricin环(SRL)的27 nt模拟物,是延伸因子(EFs)结合位点的重要组成部分。现已确定野生型SRL的分辨率为1.04 A,补充了之前在1.11 A下获得的数据,并允许首次计算RNA基序的坐标误差。具有存活(C2658U·G2663A)或致死突变(C2658G·G2663C)的其他两个结构,分别以1.75和2.25 A的分辨率测定。比较表明,凸出的G基序具有常见的水合作用和几何形状,在侧面的结构元素处具有灵活的连接。六个保守的核苷酸保留了基序的折叠;其余的七到九个依次变化并改变两个凹槽中的接触。致死突变的可及功能基团与活突变和野生型SRL的可及功能基元之间的差异,可能是延伸因子与具有C2658G?G2663C突变的核糖体结合的受损的原因,并且可能是致死表型的基础。

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