Nielsen Soren, Zenkin Nikolay
Centre for Bacterial Cell Biology, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Baddiley-Clark Building, Richardson Road, Newcastle Upon Tyne NE2 4AX, UK.
Sci Adv. 2025 Aug 22;11(34):eadw2470. doi: 10.1126/sciadv.adw2470. Epub 2025 Aug 20.
RNA polymerase I (Pol I) synthesizes ribosomal RNA precursor (pre-rRNA), which comprises most of RNA in eukaryotic cells. Despite decades of investigation, there is still no consensus on what causes Pol I transcription termination. Here, we show that efficient termination by Pol I, paused by termination roadblock protein, is caused by RNA hairpin of the nascent pre-rRNA. Hairpin-dependent termination takes place at a physiological rate and does not require trans-acting factors. The function of the roadblock protein and the T-rich sequence is to synergistically cause deep backtracking of Pol I toward the termination RNA hairpin. Simultaneously, Pol I is catalytically inactivated, preventing rescue from backtracking through RNA cleavage and thus committing Pol I to termination. Termination RNA hairpins are present in most of Pol I terminators of eukaryotes, suggesting conservation of the RNA hairpin-dependent mechanism of Pol I transcription termination. We propose a simple model that unifies previous findings.
RNA聚合酶I(Pol I)合成核糖体RNA前体(pre-rRNA),它构成了真核细胞中大部分的RNA。尽管经过了数十年的研究,但对于导致Pol I转录终止的原因仍未达成共识。在这里,我们表明,被终止阻碍蛋白暂停的Pol I的有效终止是由新生pre-rRNA的RNA发夹结构引起的。依赖发夹结构的终止以生理速率发生,并且不需要反式作用因子。阻碍蛋白和富含T的序列的功能是协同导致Pol I向终止RNA发夹结构深度回溯。同时,Pol I的催化活性被灭活,阻止通过RNA切割从回溯中解救出来,从而使Pol I走向终止。终止RNA发夹结构存在于大多数真核生物的Pol I终止子中,这表明Pol I转录终止的RNA发夹结构依赖性机制具有保守性。我们提出了一个统一先前研究结果的简单模型。