Catala Mathieu, Tremblay Maxime, Samson Eric, Conconi Antonio, Abou Elela Sherif
Département de Microbiologie et d'Infectiologie, Faculté de Médecine, Université de Sherbrooke, 3001 12 Ave. Nord, Sherbrooke, Québec, Canada.
Mol Cell Biol. 2008 Jan;28(2):619-29. doi: 10.1128/MCB.01805-07. Epub 2007 Nov 8.
In Saccharomyces cerevisiae, the double-stranded-RNA-specific RNase III (Rnt1p) is required for the processing of pre-rRNA and coprecipitates with transcriptionally active rRNA gene repeats. Here we show that Rnt1p physically interacts with RNA polymerase I (RNAPI) and its deletion decreases the transcription of the rRNA gene and increases the number of rRNA genes with an open chromatin structure. In contrast, depletion of ribosomal proteins or factors that impair RNAPI termination did not increase the number of open rRNA gene repeats, suggesting that changes in the ratio of open and closed rRNA gene chromatin is not due to a nonspecific response to ribosome depletion or impaired termination. The results demonstrate that defects in pre-rRNA processing can influence the chromatin structure of the rRNA gene arrays and reveal links among the rRNA gene chromatin, transcription, and processing.
在酿酒酵母中,双链RNA特异性核糖核酸酶III(Rnt1p)是前体rRNA加工所必需的,并且与转录活性rRNA基因重复序列共沉淀。我们在此表明,Rnt1p与RNA聚合酶I(RNAPI)发生物理相互作用,其缺失会降低rRNA基因的转录,并增加具有开放染色质结构的rRNA基因数量。相比之下,核糖体蛋白的消耗或损害RNAPI终止的因子并没有增加开放的rRNA基因重复序列的数量,这表明开放和封闭的rRNA基因染色质比例的变化并非由于对核糖体消耗或终止受损的非特异性反应。这些结果表明,前体rRNA加工缺陷可影响rRNA基因阵列的染色质结构,并揭示了rRNA基因染色质、转录和加工之间的联系。