Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, UK.
Institute of Molecular Cancer Research, University of Zurich, 8057 Zurich, Switzerland.
Nucleic Acids Res. 2021 Oct 11;49(18):10477-10492. doi: 10.1093/nar/gkab771.
ADP-ribosylation is a modification that targets a variety of macromolecules and regulates a diverse array of important cellular processes. ADP-ribosylation is catalysed by ADP-ribosyltransferases and reversed by ADP-ribosylhydrolases. Recently, an ADP-ribosyltransferase toxin termed 'DarT' from bacteria, which is distantly related to human PARPs, was shown to modify thymidine in single-stranded DNA in a sequence specific manner. The antitoxin of DarT is the macrodomain containing ADP-ribosylhydrolase DarG, which shares striking structural homology with the human ADP-ribosylhydrolase TARG1. Here, we show that TARG1, like DarG, can reverse thymidine-linked DNA ADP-ribosylation. We find that TARG1-deficient human cells are extremely sensitive to DNA ADP-ribosylation. Furthermore, we also demonstrate the first detection of reversible ADP-ribosylation on genomic DNA in vivo from human cells. Collectively, our results elucidate the impact of DNA ADP-ribosylation in human cells and provides a molecular toolkit for future studies into this largely unknown facet of ADP-ribosylation.
ADP-核糖基化是一种针对多种生物大分子的修饰方式,可调节多种重要的细胞过程。ADP-核糖基化由 ADP-核糖基转移酶催化,由 ADP-核糖基水解酶逆转。最近,从细菌中分离出一种名为“DarT”的 ADP-核糖基转移酶毒素,它与人类 PARPs 有一定的亲缘关系,被证明能够以序列特异性的方式修饰单链 DNA 中的胸苷。DarT 的抗毒素是含有 ADP-核糖基水解酶结构域的 DarG,它与人类 ADP-核糖基水解酶 TARG1 具有惊人的结构同源性。在这里,我们表明 TARG1 与 DarG 一样,可以逆转与胸苷相连的 DNA ADP-核糖基化。我们发现 TARG1 缺陷的人类细胞对 DNA ADP-核糖基化极其敏感。此外,我们还首次在体内从人类细胞中检测到基因组 DNA 上可逆的 ADP-核糖基化。总之,我们的研究结果阐明了 DNA ADP-核糖基化在人类细胞中的作用,并为未来对这一未知 ADP-核糖基化领域的研究提供了分子工具。