Centre for mRNP Biogenesis and Metabolism, Department of Molecular Biology, Aarhus University, Aarhus DK-8000, Denmark.
Mol Cell. 2010 Feb 26;37(4):580-7. doi: 10.1016/j.molcel.2010.01.019.
Termination of RNA polymerase II (RNAPII) transcription of protein-coding genes occurs downstream of cleavage/polyadenylation sites. According to the "torpedo" model, the 5'-3' exonuclease Rat1p/Xrn2p attacks the newly formed 5' end of the cleaved pre-mRNA, causing the still transcribing RNAPII to terminate. Here we demonstrate a similar role of S. cerevisiae Rat1p within the gene body. We find that the transcription processivity defect imposed on RNAPII by the rpb1-N488D mutation is corrected upon Rat1p inactivation. Importantly, Rat1p-dependent transcription termination occurs upstream the polyadenylation site. Genetic and biochemical evidence demonstrate that mRNA capping is defective in rpb1-N488D cells, which leads to increased levels of Rat1p all along the gene locus. Consistently, Rat1p-dependent RNAPII termination is also observed in the capping-deficient ceg1-63 strain. Our data suggest that Rat1p serves to terminate RNAPII molecules engaged in the production of uncapped RNA, regardless of their position on the gene locus.
RNA 聚合酶 II(RNAPII)对蛋白质编码基因的转录在切割/多聚腺苷酸化位点的下游终止。根据“鱼雷”模型,5'-3'外切酶 Rat1p/Xrn2p 攻击刚形成的切割前 mRNA 的 5' 端,导致仍在转录的 RNAPII 终止。在这里,我们证明了酿酒酵母 Rat1p 在基因体内具有类似的作用。我们发现,rpb1-N488D 突变对 RNAPII 造成的转录连续性缺陷在 Rat1p 失活后得到纠正。重要的是,Rat1p 依赖性转录终止发生在多聚腺苷酸化位点的上游。遗传和生化证据表明,rpb1-N488D 细胞中的 mRNA 加帽有缺陷,这导致 Rat1p 在整个基因座上的水平增加。一致地,在加帽缺陷的 ceg1-63 菌株中也观察到 Rat1p 依赖性 RNAPII 终止。我们的数据表明,Rat1p 可终止参与无帽 RNA 生成的 RNAPII 分子,而不论其在基因座上的位置如何。