Mendoza Oscar, Bourdoncle Anne, Boulé Jean-Baptiste, Brosh Robert M, Mergny Jean-Louis
University of Bordeaux, ARNA Laboratory F-33000 Bordeaux, France INSERM U1212,CNRS UMR 5320, IECB, F-33600 Pessac, France.
CNRS UMR 7196, INSERM U1154, MNHN, F-75005 Paris, France Sorbonne Universités, F-75005 Paris, France
Nucleic Acids Res. 2016 Mar 18;44(5):1989-2006. doi: 10.1093/nar/gkw079. Epub 2016 Feb 15.
Guanine-rich DNA strands can fold in vitro into non-canonical DNA structures called G-quadruplexes. These structures may be very stable under physiological conditions. Evidence suggests that G-quadruplex structures may act as 'knots' within genomic DNA, and it has been hypothesized that proteins may have evolved to remove these structures. The first indication of how G-quadruplex structures could be unfolded enzymatically came in the late 1990s with reports that some well-known duplex DNA helicases resolved these structures in vitro. Since then, the number of studies reporting G-quadruplex DNA unfolding by helicase enzymes has rapidly increased. The present review aims to present a general overview of the helicase/G-quadruplex field.
富含鸟嘌呤的DNA链在体外可折叠成称为G-四链体的非经典DNA结构。这些结构在生理条件下可能非常稳定。有证据表明,G-四链体结构可能在基因组DNA中充当“结”,并且有人推测蛋白质可能已经进化以去除这些结构。关于G-四链体结构如何通过酶促方式解折叠的首个迹象出现在20世纪90年代末,当时有报道称一些著名的双链DNA解旋酶在体外可解析这些结构。从那时起,报道解旋酶酶促展开G-四链体DNA的研究数量迅速增加。本综述旨在对解旋酶/G-四链体领域进行总体概述。