Delint-Ramirez Ilse, Madabhushi Ram
Departments of Psychiatry, Neuroscience, and Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA; Peter O' Donnell Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Departments of Psychiatry, Neuroscience, and Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA; Peter O' Donnell Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Neuron. 2025 Jan 8;113(1):7-28. doi: 10.1016/j.neuron.2024.12.001.
DNA damage is a major risk factor for the decline of neuronal functions with age and in neurodegenerative diseases. While how DNA damage causes neurodegeneration is still being investigated, innovations over the past decade have provided significant insights into this issue. Breakthroughs in next-generation sequencing methods have begun to reveal the characteristics of neuronal DNA damage hotspots and the causes of DNA damage. Chromosome conformation capture-based approaches have shown that, while DNA damage and the ensuing cellular response alter chromatin topology, chromatin organization at damage sites also affects DNA repair outcomes in neurons. Additionally, neuronal activity results in the formation of programmed DNA breaks, which could burden DNA repair mechanisms and promote neuronal dysfunction. Finally, emerging evidence implicates DNA damage-induced inflammation as an important contributor to the age-related decline in neuronal functions. Together, these discoveries have ushered in a new understanding of the significance of genome maintenance for neuronal function.
DNA损伤是神经元功能随年龄增长及在神经退行性疾病中衰退的主要风险因素。虽然DNA损伤如何导致神经退行性变仍在研究中,但过去十年的创新为这一问题提供了重要见解。新一代测序方法的突破已开始揭示神经元DNA损伤热点的特征及DNA损伤的原因。基于染色体构象捕获的方法表明,虽然DNA损伤及随后的细胞反应会改变染色质拓扑结构,但损伤部位的染色质组织也会影响神经元中的DNA修复结果。此外,神经元活动会导致程序性DNA断裂的形成,这可能会加重DNA修复机制的负担并促进神经元功能障碍。最后,新出现的证据表明,DNA损伤诱导的炎症是神经元功能与年龄相关衰退的重要促成因素。总之,这些发现带来了对基因组维持对神经元功能重要性的新认识。