MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH, UK.
Genes (Basel). 2019 Jan 29;10(2):95. doi: 10.3390/genes10020095.
A cursory look at any textbook image of DNA replication might suggest that the complex machine that is the replisome runs smoothly along the chromosomal DNA. However, many DNA sequences can adopt non-B form secondary structures and these have the potential to impede progression of the replisome. A picture is emerging in which the maintenance of processive DNA replication requires the action of a significant number of additional proteins beyond the core replisome to resolve secondary structures in the DNA template. By ensuring that DNA synthesis remains closely coupled to DNA unwinding by the replicative helicase, these factors prevent impediments to the replisome from causing genetic and epigenetic instability. This review considers the circumstances in which DNA forms secondary structures, the potential responses of the eukaryotic replisome to these impediments in the light of recent advances in our understanding of its structure and operation and the mechanisms cells deploy to remove secondary structure from the DNA. To illustrate the principles involved, we focus on one of the best understood DNA secondary structures, G quadruplexes (G4s), and on the helicases that promote their resolution.
乍一看,任何一本教科书上关于 DNA 复制的图片可能都表明,复制体这一复杂的机器可以沿着染色体 DNA 平稳运行。然而,许多 DNA 序列可以采用非 B 型二级结构,这些结构有可能阻碍复制体的前进。目前的情况是,为了维持连续的 DNA 复制,除了核心复制体之外,还需要大量额外的蛋白质来解决 DNA 模板中的二级结构。通过确保 DNA 合成与复制性解旋酶的 DNA 解旋紧密偶联,这些因素可以防止复制体受阻导致遗传和表观遗传不稳定。这篇综述考虑了 DNA 形成二级结构的情况,以及真核复制体在了解其结构和功能方面的最新进展的基础上,对这些障碍的潜在反应,以及细胞用来从 DNA 中去除二级结构的机制。为了说明所涉及的原理,我们重点介绍了最被理解的 DNA 二级结构之一——G 四联体(G4s),以及促进其解析的解旋酶。