Department. of Biology, Tufts University, Medford, MA 02155, USA.
Cells. 2020 Jul 9;9(7):1657. doi: 10.3390/cells9071657.
Double-strand breaks are one of the most deleterious DNA lesions. Their repair via error-prone mechanisms can promote mutagenesis, loss of genetic information, and deregulation of the genome. These detrimental outcomes are significant drivers of human diseases, including many cancers. Mutagenic double-strand break repair also facilitates heritable genetic changes that drive organismal adaptation and evolution. In this review, we discuss the mechanisms of various error-prone DNA double-strand break repair processes and the cellular conditions that regulate them, with a focus on alternative end joining. We provide examples that illustrate how mutagenic double-strand break repair drives genome diversity and evolution. Finally, we discuss how error-prone break repair can be crucial to the induction and progression of diseases such as cancer.
双链断裂是最具危害性的 DNA 损伤之一。通过易错机制进行修复会促进突变、遗传信息丢失和基因组失稳。这些有害后果是导致人类疾病的重要因素,包括许多癌症。具有突变性的双链断裂修复还促进了驱动生物适应性和进化的可遗传性遗传变化。在这篇综述中,我们讨论了各种易错 DNA 双链断裂修复过程的机制,以及调节这些过程的细胞条件,重点讨论了非同源末端连接。我们提供了一些例子来说明突变性双链断裂修复如何驱动基因组多样性和进化。最后,我们讨论了易错性断裂修复如何对癌症等疾病的诱导和进展至关重要。