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Quantitative analysis of snoRNA association with pre-ribosomes and release of snR30 by Rok1 helicase

机译:Rok1解旋酶定量分析snoRNA与前核糖体的缔合和snR30的释放

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摘要

In yeast, three small nucleolar RNAs (snoRNAs) are essential for the processing of pre-ribosomal RNA—U3, U14 and snR30—whereas 72 non-essential snoRNAs direct site-specific modification of pre-rRNA. We applied a quantitative screen for alterations in the pre-ribosome association to all 75 yeast snoRNAs in strains depleted of eight putative helicases implicated in 40S subunit synthesis. For the modification-guide snoRNAs, we found no clear evidence for the involvement of these helicases in the association or dissociation of pre-ribosomes. However, the DEAD box helicase Rok1 was required specifically for the release of snR30. Point mutations in motif I, but not in motif III, of the helicase domain of Rok1 impaired the release of snR30, but this was less marked than in strains depleted of Rok1, and resulted in a dominant-negative growth phenotype. Dissociation of U3 and U14 from pre-ribosomes is also dependent on helicases, suggesting that release of the essential snoRNAs might differ mechanistically from release of the modification-guide snoRNAs.
机译:在酵母中,三个小核仁RNA(snoRNA)对于核糖体前RNA的加工是必不可少的-U3,U14和snR30,而72个非必需snoRNA则指导前rRNA的位点特异性修饰。我们应用了一种定量筛选方法,筛选了缺失了涉及40S亚基合成的八种假定解旋酶的菌株中的所有75个酵母snoRNA的核糖体前缔合变化。对于修饰指导的snoRNA,我们没有发现明确的证据表明这些解旋酶参与了核糖体前体的结合或解离。但是,DEAD盒解旋酶Rok1是释放snR30所特有的。 Rok1的解旋酶结构域的基序I中的点突变,而不是基序III中的点突变,损害了snR30的释放,但它比耗竭Rok1的菌株中的标记突变少,并导致显性阴性的生长表型。 U3和U14与核糖体前体的解离也取决于解旋酶,表明必需snoRNA的释放可能与修饰指导snoRNA的释放机理不同。

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