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Mammalian DEAD Box Protein Ddx51 Acts in 3′ End Maturation of 28S rRNA by Promoting the Release of U8 snoRNA ▿ §

机译:哺乳动物DEAD盒蛋白Ddx51通过促进U8 snoRNA的释放在28S rRNA的3'端成熟中起作用

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摘要

Biogenesis of eukaryotic ribosomes requires a number of RNA helicases that drive molecular rearrangements at various points of the assembly pathway. While many ribosome synthesis factors are conserved among all eukaryotes, certain features of ribosome maturation, such as U8 snoRNA-assisted processing of the 5.8S and 28S rRNA precursors, are observed only in metazoan cells. Here, we identify the mammalian DEAD box helicase family member Ddx51 as a novel ribosome synthesis factor and an interacting partner of the nucleolar GTP-binding protein Nog1. Unlike any previously studied yeast helicases, Ddx51 is required for the formation of the 3′ end of 28S rRNA. Ddx51 binds to pre-60S subunit complexes and promotes displacement of U8 snoRNA from pre-rRNA, which is necessary for the removal of the 3′ external transcribed spacer from 28S rRNA and productive downstream processing. These data demonstrate the emergence of a novel factor that facilitates a pre-rRNA processing event specific for higher eukaryotes.
机译:真核生物核糖体的生物发生需要许多RNA解旋酶,这些解旋酶在组装途径的各个点驱动分子重排。尽管在所有真核生物中许多核糖体合成因子均被保守,但仅在后生细胞中观察到了核糖体成熟的某些特征,例如5.8S和28S rRNA前体的U8 snoRNA辅助加工。在这里,我们确定哺乳动物DEAD框解旋酶家族成员Ddx51为新型核糖体合成因子和核仁GTP结合蛋白Nog1的相互作用伙伴。与以前研究的任何酵母解旋酶不同,Ddx51是28S rRNA 3'末端形成所必需的。 Ddx51结合60S之前的亚基复合物,并促进U8 snoRNA从pre-rRNA的置换,这对于从28S rRNA去除3'外部转录间隔子和生产性下游加工是必需的。这些数据证明了一种新型因子的出现,该因子促进了针对高等真核生物的前rRNA加工事件。

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