Aiello Umberto, Porrua Odil, Libri Domenico
Stanford University School of Medicine, Department of Genetics, Stanford, CA, USA.
Institut de Génétique Moléculaire de Montpellier, Univ Montpellier, CNRS, Montpellier, France.
J Mol Biol. 2025 Jan 1;437(1):168808. doi: 10.1016/j.jmb.2024.168808. Epub 2024 Sep 30.
Several machineries concurrently work on the DNA, but among them RNA Polymerases (RNAPs) are the most widespread and active users. The homeostasis of such a busy genomic environment relies on the existence of mechanisms that allow limiting transcription to a functional level, both in terms of extent and rate. Sen1 is a central player in this sense: using its translocase activity this protein has evolved the specific function of dislodging RNAPs from the DNA template, thus ending the transcription cycle. Over the years, studies have shown that Sen1 uses this same mechanism in a multitude of situations, allowing termination of all three eukaryotic RNAPs in different contexts. In virtue of its helicase activity, Sen1 has also been proposed to have a prominent function in the resolution of co-transcriptional genotoxic R-loops, which can cause the stalling of replication forks. In this review, we provide a synopsis of past and recent findings on the functions of Sen1 in yeast and of its human homologue Senataxin (SETX).
几种机制同时作用于DNA,但其中RNA聚合酶(RNAPs)是分布最广且最活跃的使用者。在这样一个繁忙的基因组环境中,稳态依赖于一些机制的存在,这些机制能够在范围和速率方面将转录限制在功能水平。从这个意义上说,Sen1是核心参与者:利用其转位酶活性,这种蛋白质进化出了将RNAPs从DNA模板上移除的特定功能,从而结束转录周期。多年来,研究表明Sen1在多种情况下都使用这一相同机制,可在不同背景下终止所有三种真核生物的RNAPs。由于其解旋酶活性,Sen1还被认为在解决共转录基因毒性R环方面具有重要作用,R环可导致复制叉停滞。在这篇综述中,我们概述了过去和最近关于Sen1在酵母中的功能及其人类同源物Senataxin(SETX)的研究发现。