Laboratory of Signaling and Gene Regulation, Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Division of Basic Research, Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China.
Laboratory of Signaling and Gene Regulation, Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Division of Basic Research, Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Mol Cell. 2022 Jun 16;82(12):2315-2334. doi: 10.1016/j.molcel.2022.02.021. Epub 2022 Mar 9.
ADP-ribosylation (ADPRylation) is a post-translational modification of proteins catalyzed by ADP-ribosyl transferase (ART) enzymes, including nuclear PARPs (e.g., PARP1 and PARP2). Historically, studies of ADPRylation and PARPs have focused on DNA damage responses in cancers, but more recent studies elucidate diverse roles in a broader array of biological processes. Here, we summarize the expanding array of molecular mechanisms underlying the biological functions of nuclear PARPs with a focus on PARP1, the founding member of the family. This includes roles in DNA repair, chromatin regulation, gene expression, ribosome biogenesis, and RNA biology. We also present new concepts in PARP1-dependent regulation, including PAR-dependent post-translational modifications, "ADPR spray," and PAR-mediated biomolecular condensate formation. Moreover, we review advances in the therapeutic mechanisms of PARP inhibitors (PARPi) as well as the progress on the mechanisms of PARPi resistance. Collectively, the recent progress in the field has yielded new insights into the expanding universe of PARP1-mediated molecular and therapeutic mechanisms in a variety of biological processes.
ADP-核糖基化(ADPRylation)是一种由 ADP-核糖基转移酶(ART)酶催化的蛋白质翻译后修饰,包括核 PARPs(例如,PARP1 和 PARP2)。历史上,ADPRylation 和 PARPs 的研究集中在癌症中的 DNA 损伤反应上,但最近的研究阐明了它们在更广泛的生物学过程中的多种作用。在这里,我们总结了核 PARPs 的生物学功能的分子机制的扩展,重点是家族的创始成员 PARP1。这包括在 DNA 修复、染色质调节、基因表达、核糖体生物发生和 RNA 生物学中的作用。我们还介绍了 PARP1 依赖性调节的新概念,包括 PAR 依赖性翻译后修饰、“ADPR 喷雾”和 PAR 介导的生物分子凝聚物形成。此外,我们回顾了 PARP 抑制剂(PARPi)的治疗机制的进展以及 PARPi 耐药机制的进展。总之,该领域的最新进展为各种生物学过程中 PARP1 介导的分子和治疗机制的扩展宇宙提供了新的见解。