Department of Biology, Stanford University, 371 Serra Mall, Stanford, CA, 94305-5020, United States.
Department of Biology, Stanford University, 371 Serra Mall, Stanford, CA, 94305-5020, United States.
DNA Repair (Amst). 2018 Nov;71:69-81. doi: 10.1016/j.dnarep.2018.08.009. Epub 2018 Aug 25.
R-loops are structures consisting of an RNA-DNA duplex and an unpaired DNA strand. They can form during transcription upon nascent RNA "threadback" invasion into the DNA duplex to displace the non-template strand. Although R-loops occur naturally in all kingdoms of life and serve regulatory roles, they are often deleterious and can cause genomic instability. Of particular importance are the disastrous consequences when replication forks or transcription complexes collide with R-loops. The appropriate processing of R-loops is essential to avoid a number of human neurodegenerative and other clinical disorders. We provide a perspective on mechanistic aspects of R-loop formation and their resolution learned from studies in model systems. This should contribute to improved understanding of R-loop biological functions and enable their practical applications. We propose the novel employment of artificially-generated stable R-loops to selectively inactivate tumor cells.
R 环是由 RNA-DNA 双链体和一条未配对的 DNA 链组成的结构。它们可以在转录过程中形成,当新生 RNA“回穿”侵入 DNA 双链体时,会取代非模板链。尽管 R 环在所有生命领域中自然存在,并发挥着调节作用,但它们通常是有害的,并可能导致基因组不稳定。当复制叉或转录复合物与 R 环碰撞时,会产生特别严重的后果。适当处理 R 环对于避免许多人类神经退行性疾病和其他临床疾病至关重要。我们从模型系统的研究中提供了对 R 环形成及其解决的机制方面的观点。这应该有助于提高对 R 环生物学功能的理解,并使它们能够得到实际应用。我们建议利用人工产生的稳定 R 环来选择性地灭活肿瘤细胞。