Ballarino Monica, Morlando Mariangela, Pagano Francesca, Fatica Alessandro, Bozzoni Irene
Institute Pasteur Fondazione Cenci-Bolognetti, Department of Genetics and Molecular Biology, University La Sapienza, P.le A. Moro 5, 00185 Rome, Italy.
Mol Cell Biol. 2005 Jul;25(13):5396-403. doi: 10.1128/MCB.25.13.5396-5403.2005.
The carboxy-terminal domain (CTD) of RNA polymerase II large subunit acts as a platform to assemble the RNA processing machinery in a controlled way throughout the transcription cycle. In yeast, recent findings revealed a physical connection between phospho-CTD, generated by the Ctk1p kinase, and protein factors having a function in small nucleolar RNA (snoRNA) biogenesis. The snoRNAs represent a large family of polymerase II noncoding transcripts that are associated with highly conserved polypeptides to form stable ribonucleoprotein particles (snoRNPs). In this work, we have studied the biogenesis of the snoRNPs belonging to the box H/ACA class. We report that the assembly factor Naf1p and the core components Cbf5p and Nhp2p are recruited on H/ACA snoRNA genes very early during transcription. We also show that the cotranscriptional recruitment of Naf1p and Cbf5p is Ctk1p dependent and that Ctk1p and Cbf5p are required for preventing the readthrough into the snoRNA downstream genes. All these data suggest that proper cotranscriptional snoRNP assembly controls 3'-end formation of snoRNAs and, consequently, the release of a functional particle.
RNA聚合酶II大亚基的羧基末端结构域(CTD)作为一个平台,在整个转录周期中以可控方式组装RNA加工机制。在酵母中,最近的研究发现揭示了由Ctk1p激酶产生的磷酸化CTD与在小核仁RNA(snoRNA)生物合成中起作用的蛋白质因子之间存在物理联系。snoRNA代表了一大类聚合酶II非编码转录本,它们与高度保守的多肽相关联,形成稳定的核糖核蛋白颗粒(snoRNP)。在这项工作中,我们研究了属于盒H/ACA类的snoRNP的生物合成。我们报告称,组装因子Naf1p以及核心组分Cbf5p和Nhp2p在转录早期就被招募到H/ACA snoRNA基因上。我们还表明,Naf1p和Cbf5p的共转录招募依赖于Ctk1p,并且Ctk1p和Cbf5p是防止转录通读至snoRNA下游基因所必需的。所有这些数据表明,适当的共转录snoRNP组装控制着snoRNA的3'末端形成,从而控制着功能性颗粒的释放。