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Nop6,90S 前核糖体颗粒的一个组成部分,是酿酒酵母 40S 核糖体亚基生物发生所必需的。

Nop6, a component of 90S pre-ribosomal particles, is required for 40S ribosomal subunit biogenesis in Saccharomyces cerevisiae.

机构信息

Departamento de Genética, Universidad de Sevilla, Sevilla, Spain.

出版信息

RNA Biol. 2011 Jan-Feb;8(1):112-24. doi: 10.4161/rna.8.1.14143. Epub 2011 Jan 1.

Abstract

In Saccharomyces cerevisiae, ribosome biogenesis requires, in addition to rRNA and ribosomal proteins, a myriad of small nucleolar RNAs (snoRNAs) and over two hundred protein trans-acting factors. There are protein trans-acting factors predicted to participate in ribosome biogenesis that have not been so far characterized. Here, we report the functional analysis of the Nucleolar protein 6 (Nop6) in ribosome biogenesis. Our results show that Nop6 is needed for optimal 40S ribosomal subunit biogenesis. Deletion of NOP6 leads to an appropriate 20% reduction in 18S rRNA levels and therefore in 40S ribosomal subunits. This is due to mild inhibition of pre-rRNA processing at cleavage site A 2. Tandem affinity purification followed by mass spectrometry and northern blot analyses indicate that Nop6 is a component of 90S pre-ribosomal particles. rDNA chromatin immunoprecipitation experiments and analysis of the intracellular localisation of Nop6-eGFP after in vivo shut down of pre-rRNA transcription strongly suggest that Nop6 binds to the pre-rRNA early during transcription. Genetic data suggest that Nop6 and the snoRNA snR57 both interact similarly with the protein trans-acting factor Nep1. It has been proposed that snR57 and Nep1 participate in a pre-rRNA conformational switch that allows the proper assembly of 40S ribosomal protein S19. Our results strongly suggest that the role Nop6 might have in this conformational switch is independent of snR57.

摘要

在酿酒酵母中,核糖体生物发生除了需要 rRNA 和核糖体蛋白外,还需要大量的小核仁 RNA(snoRNA)和两百多种蛋白质转录因子。有预测表明有一些参与核糖体生物发生的蛋白质转录因子尚未得到充分表征。在这里,我们报告了核仁蛋白 6(Nop6)在核糖体生物发生中的功能分析。我们的结果表明,Nop6 是 40S 核糖体亚基生物发生所必需的。NOP6 的缺失导致 18S rRNA 水平适当降低 20%,因此 40S 核糖体亚基也减少。这是由于 pre-rRNA 在切割位点 A2 的加工受到轻微抑制所致。串联亲和纯化结合质谱和 northern blot 分析表明,Nop6 是 90S 前核糖体颗粒的组成部分。rDNA 染色质免疫沉淀实验和体内 pre-rRNA 转录关闭后 Nop6-eGFP 的细胞内定位分析强烈表明,Nop6 在转录早期与 pre-rRNA 结合。遗传数据表明,Nop6 和 snoRNA snR57 都与蛋白质转录因子 Nep1 以相似的方式相互作用。有人提出,snR57 和 Nep1 参与 pre-rRNA 构象转换,从而允许正确组装 40S 核糖体蛋白 S19。我们的结果强烈表明,Nop6 在这种构象转换中的作用独立于 snR57。

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