McClendon A Kathleen, Osheroff Neil
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232-0146, USA.
Mutat Res. 2007 Oct 1;623(1-2):83-97. doi: 10.1016/j.mrfmmm.2007.06.009. Epub 2007 Jul 3.
Type II topoisomerases are ubiquitous enzymes that play essential roles in a number of fundamental DNA processes. They regulate DNA under- and overwinding, and resolve knots and tangles in the genetic material by passing an intact double helix through a transient double-stranded break that they generate in a separate segment of DNA. Because type II topoisomerases generate DNA strand breaks as a requisite intermediate in their catalytic cycle, they have the potential to fragment the genome every time they function. Thus, while these enzymes are essential to the survival of proliferating cells, they also have significant genotoxic effects. This latter aspect of type II topoisomerase has been exploited for the development of several classes of anticancer drugs that are widely employed for the clinical treatment of human malignancies. However, considerable evidence indicates that these enzymes also trigger specific leukemic chromosomal translocations. In light of the impact, both positive and negative, of type II topoisomerases on human cells, it is important to understand how these enzymes function and how their actions can destabilize the genome. This article discusses both aspects of human type II topoisomerases.
II型拓扑异构酶是普遍存在的酶,在许多基本的DNA过程中发挥着重要作用。它们调节DNA的欠旋和过旋,并通过使完整的双螺旋穿过它们在DNA的另一个片段中产生的瞬时双链断裂来解开遗传物质中的结和缠结。由于II型拓扑异构酶在其催化循环中产生DNA链断裂作为必要的中间体,它们每次发挥作用时都有可能使基因组片段化。因此,虽然这些酶对增殖细胞的存活至关重要,但它们也具有显著的基因毒性作用。II型拓扑异构酶的后一个方面已被用于开发几类抗癌药物,这些药物广泛用于人类恶性肿瘤的临床治疗。然而,大量证据表明这些酶也会引发特定的白血病染色体易位。鉴于II型拓扑异构酶对人类细胞的积极和消极影响,了解这些酶如何发挥作用以及它们的作用如何使基因组不稳定非常重要。本文讨论了人类II型拓扑异构酶的这两个方面。