Istituto di Genetica Molecolare "Luigi Luca Cavalli-Sforza", CNR, 27100 Pavia, Italy.
Int J Mol Sci. 2020 Feb 22;21(4):1506. doi: 10.3390/ijms21041506.
Replicating the entire genome is one of the most complex tasks for all organisms. Research carried out in the last few years has provided us with a clearer picture on how cells preserve genomic information from the numerous insults that may endanger its stability. Different DNA repair pathways, coping with exogenous or endogenous threat, have been dissected at the molecular level. More recently, there has been an increasing interest towards intrinsic obstacles to genome replication, paving the way to a novel view on genomic stability. Indeed, in some cases, the movement of the replication fork can be hindered by the presence of stable DNA: RNA hybrids (R-loops), the folding of G-rich sequences into G-quadruplex structures (G4s) or repetitive elements present at Common Fragile Sites (CFS). Although differing in their nature and in the way they affect the replication fork, all of these obstacles are a source of replication stress. Replication stress is one of the main hallmarks of cancer and its prevention is becoming increasingly important as a target for future chemotherapeutics. Here we will try to summarize how these three obstacles are generated and how the cells handle replication stress upon their encounter. Finally, we will consider their role in cancer and their exploitation in current chemotherapeutic approaches.
复制整个基因组是所有生物体中最复杂的任务之一。在过去的几年中,研究已经使我们更清楚地了解细胞如何保护基因组信息免受可能威胁其稳定性的众多损伤。不同的 DNA 修复途径,应对外源性或内源性威胁,已在分子水平上进行了剖析。最近,人们对基因组复制的内在障碍越来越感兴趣,为基因组稳定性提供了新的认识。事实上,在某些情况下,复制叉的移动可能会受到稳定的 DNA:RNA 杂交物(R 环)、富含 G 序列折叠成 G-四链体结构(G4s)或常见脆性位点(CFS)中存在的重复元件的阻碍。尽管它们在性质和影响复制叉的方式上有所不同,但所有这些障碍都是复制应激的来源。复制应激是癌症的主要特征之一,作为未来化疗药物的靶点,其预防变得越来越重要。在这里,我们将尝试总结这三种障碍是如何产生的,以及细胞在遇到它们时如何处理复制应激。最后,我们将考虑它们在癌症中的作用以及它们在当前化疗方法中的应用。