Capranico Giovanni, Ferri Francesca, Fogli Maria Vittoria, Russo Alessandra, Lotito Luca, Baranello Laura
Department of Biochemistry, University of Bologna, via Irnerio 48, 40126 Bologna, Italy.
Biochimie. 2007 Apr;89(4):482-9. doi: 10.1016/j.biochi.2007.01.001. Epub 2007 Jan 21.
Eukaryotic DNA topoisomerase I is active in transcribed chromatin domains to modulate transcription-generated DNA torsional tension. Camptothecin and other agents targeting DNA topoisomerase I are used in the treatment of human solid cancers with significant clinical efficacy. Major progress has been achieved in recent years in the understanding of enzyme structures and basic cellular functions of DNA topoisomerase I. Nevertheless, the precise enzyme functions and mechanisms during transcription-related processes remain unclear. The current understanding of the molecular action of camptothecin emphasizes the drug action against the enzyme and the production of irreversible breaks in the cellular DNA. However, the high drug potency is hardly fully explained by the DNA damage outcome only. In the recent past, several unexpected findings have been reported in relation to the role of eukaryotic topoisomerase I during transcription. In particular, the function of DNA topoisomerase I and the molecular effects of its inhibition on transcription-coupled processes constitute a very active research area. Here, we will briefly review relevant investigations on topoisomerase I involvement in different stages of transcription, discussing both enzyme functions and drug effects on molecular processes.
真核生物DNA拓扑异构酶I在转录染色质结构域中发挥作用,以调节转录产生的DNA扭转张力。喜树碱和其他靶向DNA拓扑异构酶I的药物被用于治疗人类实体癌,具有显著的临床疗效。近年来,在对DNA拓扑异构酶I的酶结构和基本细胞功能的理解方面取得了重大进展。然而,在转录相关过程中该酶的确切功能和机制仍不清楚。目前对喜树碱分子作用的理解强调了药物对该酶的作用以及在细胞DNA中产生不可逆的断裂。然而,仅DNA损伤结果很难完全解释该药物的高效性。最近,有几项关于真核拓扑异构酶I在转录过程中作用的意外发现被报道。特别是,DNA拓扑异构酶I的功能及其抑制对转录偶联过程的分子效应构成了一个非常活跃的研究领域。在这里,我们将简要回顾关于拓扑异构酶I参与转录不同阶段的相关研究,讨论酶的功能和药物对分子过程的影响。