Department of Experimental Radiation Oncology, the University of Texas, MD Anderson Cancer, Houston, TX 77030, USA.
Department of Epigenetics and Molecular Carcinogenesis, the University of Texas, MD Anderson Cancer, Houston, TX 77030, USA.
Mol Cell. 2020 Dec 17;80(6):1013-1024.e6. doi: 10.1016/j.molcel.2020.11.040.
Impaired DNA crosslink repair leads to Fanconi anemia (FA), characterized by a unique manifestation of bone marrow failure and pancytopenia among diseases caused by DNA damage response defects. As a germline disorder, why the hematopoietic hierarchy is specifically affected is not fully understood. We find that reprogramming transcription during hematopoietic differentiation results in an overload of genotoxic stress, which causes aborted differentiation and depletion of FA mutant progenitor cells. DNA damage onset most likely arises from formaldehyde, an obligate by-product of oxidative protein demethylation during transcription regulation. Our results demonstrate that rapid and extensive transcription reprogramming associated with hematopoietic differentiation poses a major threat to genome stability and cell viability in the absence of the FA pathway. The connection between differentiation and DNA damage accumulation reveals a novel mechanism of genome scarring and is critical to exploring therapies to counteract the aplastic anemia for the treatment of FA patients.
DNA 交联修复受损会导致范可尼贫血(FA),其特征是骨髓衰竭和全血细胞减少,这是由 DNA 损伤反应缺陷引起的疾病中的一种独特表现。作为一种种系疾病,为什么造血系统会受到特别影响还不完全清楚。我们发现,造血分化过程中的转录重编程会导致遗传毒性应激的过载,从而导致 FA 突变祖细胞的分化中止和耗竭。DNA 损伤的发生很可能源自甲醛,这是转录调控过程中氧化蛋白去甲基化的必需副产物。我们的研究结果表明,与造血分化相关的快速而广泛的转录重编程对 FA 通路缺失时的基因组稳定性和细胞活力构成了重大威胁。分化和 DNA 损伤积累之间的联系揭示了一种基因组损伤的新机制,这对于探索治疗 FA 患者的再生障碍性贫血的疗法至关重要。