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DNA拓扑异构酶I作为一种转录蛋白和一种致命的细胞毒素。

DNA topoisomerase i as a transcription protein and a lethal cellular toxin.

作者信息

Lotito Luca, Ferri Francesca, Russo Alessandra, Capranico Giovanni

机构信息

Department of Biochemistry, University of Bologna, Bologna, Italy.

出版信息

Ital J Biochem. 2007 Jun;56(2):122-9.

Abstract

DNA topoisomerase I constitutes a significant relaxing activity in nuclei of eukaryotic cells. The enzyme acts during several DNA transactions involving the generation of torsional stress in the DNA template. Moreover, antitumor agents targeting DNA topoisomerase I are used in the treatment of human cancers with significant clinical outcome. Major progress has been attained in recent years in the understanding of the basic cellular functions of DNA topoisomerase I. In particular, the consequences of topoisomerase I activity during transcription have been extensively investigated and constitute still a very active research area. Understanding of topoisomerase I inhibitors emphasizes drug activity against the enzyme, however the high drug potency cannot be explained by the DNA damage outcome only. Even though the understanding of enzyme structure has progressed in last years, however more insights into the activity of topoisomerase I poisons have not been achieved yet. Here, we will review landmark investigations on topoisomerase I involvement in different stages of the transcription process, addressing both enzyme functions as well as drug effects on molecular processes. Moreover, we will discuss recent findings on the targeting of topoisomerase I to pre-selected sites in transcribed chromatin by fusion to a sequence-specific DNA-binding protein domain.

摘要

DNA拓扑异构酶I在真核细胞的细胞核中具有重要的松弛活性。该酶在涉及DNA模板中产生扭转应力的多种DNA活动过程中发挥作用。此外,靶向DNA拓扑异构酶I的抗肿瘤药物被用于治疗人类癌症,并取得了显著的临床疗效。近年来,在理解DNA拓扑异构酶I的基本细胞功能方面取得了重大进展。特别是,拓扑异构酶I在转录过程中的活性后果已得到广泛研究,并且仍然是一个非常活跃的研究领域。对拓扑异构酶I抑制剂的理解侧重于药物对该酶的活性,然而,高药物效力不能仅用DNA损伤结果来解释。尽管近年来对酶结构的理解有所进展,但是对拓扑异构酶I毒物活性的更多见解尚未实现。在这里,我们将回顾关于拓扑异构酶I参与转录过程不同阶段的标志性研究,探讨酶的功能以及药物对分子过程的影响。此外,我们将讨论关于通过与序列特异性DNA结合蛋白结构域融合将拓扑异构酶I靶向转录染色质中预先选择位点的最新发现。

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