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Functional importance of individual rRNA 2'-O-ribose methylations revealed by high-resolution phenotyping.

机译:高分辨率表型揭示了单个rRNA 2'-O-核糖甲基化的功能重要性。

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摘要

Ribosomal RNAs contain numerous modifications at specific nucleotides. Despite their evolutionary conservation, the functional role of individual 2'-O-ribose methylations in rRNA is not known. A distinct family of small nucleolar RNAs, box C/D snoRNAs, guides the methylating complex to specific rRNA sites. Using a high-resolution phenotyping approach, we characterized 20 box C/D snoRNA gene deletions for altered growth dynamics under a wide array of environmental perturbations, encompassing intraribosomal antibiotics, inhibitors of specific cellular features, as well as general stressors. Ribosome-specific antibiotics generated phenotypes indicating different and long-ranging structural effects of rRNA methylations on the ribosome. For all studied box C/D snoRNA mutants we uncovered phenotypes to extraribosomal growth inhibitors, most frequently reflected in alteration in growth lag (adaptation time). A number of strains were highly pleiotropic and displayed a great number of sensitive phenotypes, e.g., deletion mutants of snR70 and snR71, which both have clear human homologues, and deletion mutants of snR65 and snR68. Our data indicate that individual rRNA ribose methylations can play either distinct or general roles in the workings of the ribosome.
机译:核糖体RNA在特定核苷酸处包含许多修饰。尽管有进化上的保守性,但rRNA中各个2'-O-核糖甲基化的功能作用尚不清楚。独特的小核仁RNA家族,即盒C / D snoRNA,将甲基化复合物引导至特定的rRNA位点。使用高分辨率的表型分析方法,我们表征了20个框C / D snoRNA基因缺失,可在多种环境扰动下改变生长动力学,包括核糖体内抗生素,特定细胞功能抑制剂以及一般应激源。核糖体特异性抗生素产生的表型表明,rRNA甲基化对核糖体具有不同的长期影响。对于所有研究的盒C / D snoRNA突变体,我们发现了核糖体外生长抑制剂的表型,最常反映在生长滞后的变化(适应时间)中。许多菌株是高度多效性的,并表现出许多敏感的表型,例如,snR70和snR71的缺失突变体,它们都具有清晰的人类同源性,以及snR65和snR68的缺失突变体。我们的数据表明,单个rRNA核糖甲基化可以在核糖体的工作中发挥不同或普遍的作用。

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