Donnio Lise-Marie, Giglia-Mari Giuseppina
Institut NeuroMyoGène-Pathophysiology and Genetics of Neuron and Muscle (INMG_PGNM), CNRS UMR 5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, 69008, France.
FEBS Lett. 2025 Jan;599(2):275-294. doi: 10.1002/1873-3468.14964. Epub 2024 Jul 11.
The effects of genotoxic agents on DNA and the processes involved in their removal have been thoroughly studied; however, very little is known about the mechanisms governing the reinstatement of cellular activities after DNA repair, despite restoration of the damage-induced block of transcription being essential for cell survival. In addition to impeding transcription, DNA lesions have the potential to disrupt the precise positioning of chromatin domains within the nucleus and alter the meticulously organized architecture of the nucleolus. Alongside the necessity of resuming transcription mediated by RNA polymerase 1 and 2 transcription, it is crucial to restore the structure of the nucleolus to facilitate optimal ribosome biogenesis and ensure efficient and error-free translation. Here, we examine the current understanding of how transcriptional activity from RNA polymerase 2 is reinstated following DNA repair completion and explore the mechanisms involved in reassembling the nucleolus to safeguard the correct progression of cellular functions. Given the lack of information on this vital function, this Review seeks to inspire researchers to explore deeper into this specific subject and offers essential suggestions on how to investigate this complex and nearly unexplored process further.
遗传毒性剂对DNA的影响以及去除这些遗传毒性剂所涉及的过程已得到充分研究;然而,尽管损伤诱导的转录阻滞的恢复对细胞存活至关重要,但对于DNA修复后细胞活动恢复的调控机制却知之甚少。除了阻碍转录外,DNA损伤还可能破坏染色质结构域在细胞核内的精确位置,并改变精心组织的核仁结构。除了恢复由RNA聚合酶1和2介导的转录的必要性外,恢复核仁结构以促进最佳核糖体生物发生并确保高效且无差错的翻译也至关重要。在这里,我们研究了目前对DNA修复完成后RNA聚合酶2的转录活性如何恢复的理解,并探索了参与重新组装核仁以保障细胞功能正确进展的机制。鉴于关于这一重要功能的信息匮乏,本综述旨在激励研究人员更深入地探索这一特定主题,并就如何进一步研究这一复杂且几乎未被探索的过程提供重要建议。