Preti Milena, Guffanti Elisa, Valitutto Eleonora, Dieci Giorgio
Dipartimento di Biochimica e Biologia Molecolare, Università degli Studi di Parma, 43100 Parma, Italy.
Biochem Biophys Res Commun. 2006 Dec 15;351(2):468-73. doi: 10.1016/j.bbrc.2006.10.053. Epub 2006 Oct 17.
The SNR52 gene, coding for a box C/D snoRNA, is the only snoRNA gene transcribed by RNA polymerase (Pol) III in Saccharomyces cerevisiae. Pol III transcription generates a precisely terminated primary transcript that undergoes extensive 5'-end processing. Here, we show that mutations of the box C/D core motif required for snoRNP assembly compromise 5'-end maturation of the SNR52 snoRNA. Upstream processing was also impaired by specific depletion of either Nop1p or Nop58p snoRNP proteins. We further show that the nuclear exosome is required for 3'-end maturation of SNR52 snoRNA, at variance with all the other known Pol III transcripts. Our data suggest a functional coupling between snoRNP assembly and 5'-end maturation of independently transcribed box C/D snoRNAs.
编码盒C/D小核仁RNA的SNR52基因是酿酒酵母中唯一由RNA聚合酶(Pol)III转录的小核仁RNA基因。Pol III转录产生一个精确终止的初级转录本,该转录本会经历广泛的5'端加工。在这里,我们表明,小核仁核糖核蛋白(snoRNP)组装所需的盒C/D核心基序的突变会损害SNR52小核仁RNA的5'端成熟。Nop1p或Nop58p snoRNP蛋白的特异性缺失也会损害上游加工。我们进一步表明,与所有其他已知的Pol III转录本不同,核外切体是SNR52小核仁RNA 3'端成熟所必需的。我们的数据表明,snoRNP组装与独立转录的盒C/D小核仁RNA的5'端成熟之间存在功能耦合。