Department of Molecular Biology and Genetics, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
RNA. 2011 Nov;17(11):2011-25. doi: 10.1261/rna.2840711. Epub 2011 Sep 27.
RNA polymerase II transcribes both coding and noncoding genes, and termination of these different classes of transcripts is facilitated by different sets of termination factors. Pre-mRNAs are terminated through a process that is coupled to the cleavage/polyadenylation machinery, and noncoding RNAs in the yeast Saccharomyces cerevisiae are terminated through a pathway directed by the RNA-binding proteins Nrd1, Nab3, and the RNA helicase Sen1. We have used an in vivo cross-linking approach to map the binding sites of components of the yeast non-poly(A) termination pathway. We show here that Nrd1, Nab3, and Sen1 bind to a number of noncoding RNAs in an unexpected manner. Sen1 shows a preference for H/ACA over box C/D snoRNAs. Nrd1, which binds to snoRNA terminators, also binds to the upstream region of some snoRNA transcripts and to snoRNAs embedded in introns. We present results showing that several RNAs, including the telomerase RNA TLC1, require Nrd1 for proper processing. Binding of Nrd1 to transcripts from tRNA genes is another unexpected observation. We also observe RNA polymerase II binding to transcripts from RNA polymerase III genes, indicating a possible role for the Nrd1 pathway in surveillance of transcripts synthesized by the wrong polymerase. The binding targets of Nrd1 pathway components change in the absence of glucose, with Nrd1 and Nab3 showing a preference for binding to sites in the mature snoRNA and tRNAs. This suggests a novel role for Nrd1 and Nab3 in destruction of ncRNAs in response to nutrient limitation.
RNA 聚合酶 II 转录编码和非编码基因,这些不同类别的转录本的终止是由不同的终止因子来促进的。前体 mRNA 的终止是通过与切割/多聚腺苷酸化机制偶联的过程实现的,而酵母酿酒酵母中的非多聚(A)终止途径的非编码 RNA 是通过 RNA 结合蛋白 Nrd1、Nab3 和 RNA 解旋酶 Sen1 指导的途径来终止的。我们使用体内交联方法来绘制酵母非多聚(A)终止途径成分的结合位点图谱。我们在这里表明,Nrd1、Nab3 和 Sen1 以一种意想不到的方式结合到许多非编码 RNA 上。Sen1 对 H/ACA 比对 box C/D snoRNA 表现出偏好。与 snoRNA 终止子结合的 Nrd1 也结合到一些 snoRNA 转录本的上游区域和嵌入在内含子中的 snoRNA。我们提出的结果表明,包括端粒酶 RNA TLC1 在内的几种 RNA 需要 Nrd1 才能正确加工。Nrd1 与 tRNA 基因转录本的结合是另一个意外的观察结果。我们还观察到 RNA 聚合酶 II 与 RNA 聚合酶 III 基因转录本结合,这表明 Nrd1 途径在监控由错误聚合酶合成的转录本方面可能发挥作用。在没有葡萄糖的情况下,Nrd1 途径成分的结合靶标会发生变化,Nrd1 和 Nab3 表现出对成熟 snoRNA 和 tRNA 中结合位点的偏好。这表明 Nrd1 和 Nab3 在响应营养限制时破坏 ncRNA 方面具有新的作用。