Laboratory of Molecular Gerontology, Biomedical Research Center, 251 Bayview Boulevard, National Institute on Aging, NIH, Baltimore, MD 21224, USA.
Nucleic Acids Res. 2012 Feb;40(4):1621-35. doi: 10.1093/nar/gkr844. Epub 2011 Oct 19.
DNA decatenation mediated by Topoisomerase II is required to separate the interlinked sister chromatids post-replication. SGS1, a yeast homolog of the human RecQ family of helicases interacts with Topoisomerase II and plays a role in chromosome segregation, but this functional interaction has yet to be identified in higher organisms. Here, we report a physical and functional interaction of Topoisomerase IIα with RECQL5, one of five mammalian RecQ helicases, during DNA replication. Direct interaction of RECQL5 with Topoisomerase IIα stimulates the decatenation activity of Topoisomerase IIα. Consistent with these observations, RECQL5 co-localizes with Topoisomerase IIα during S-phase of the cell cycle. Moreover, cells with stable depletions of RECQL5 display a slow proliferation rate, a G2/M cell cycle arrest and late S-phase cycling defects. Metaphase spreads generated from RECQL5-depleted cells exhibit undercondensed and entangled chromosomes. Further, RECQL5-depleted cells activate a G2/M checkpoint and undergo apoptosis. These phenotypes are similar to those observed when Topoisomerase II catalytic activity is inhibited. These results reveal an important role for RECQL5 in the maintenance of genomic stability and a new insight into the decatenation process.
DNA 解连环由拓扑异构酶 II 介导,以分离复制后相互连接的姐妹染色单体。SGS1 是酵母中与人类 RecQ 家族解旋酶同源的蛋白,与拓扑异构酶 II 相互作用,在染色体分离中发挥作用,但这种功能相互作用在高等生物中尚未被鉴定。在这里,我们报告了在 DNA 复制过程中拓扑异构酶 IIα与 RECQL5(五种哺乳动物 RecQ 解旋酶之一)之间的物理和功能相互作用。RECQL5 与拓扑异构酶 IIα 的直接相互作用刺激拓扑异构酶 IIα 的解连环活性。与这些观察结果一致,RECQL5 在细胞周期的 S 期与拓扑异构酶 IIα 共定位。此外,稳定耗尽 RECQL5 的细胞显示出增殖缓慢、G2/M 细胞周期阻滞和晚期 S 期循环缺陷。从 RECQL5 耗尽的细胞中产生的中期分裂相显示出未浓缩和纠缠的染色体。此外,RECQL5 耗尽的细胞激活 G2/M 检查点并发生细胞凋亡。这些表型类似于拓扑异构酶 II 催化活性被抑制时观察到的表型。这些结果揭示了 RECQL5 在维持基因组稳定性方面的重要作用,并为解连环过程提供了新的见解。