生物
电离辐射
染色质
赫拉
染色质重塑
DNA修复
细胞生物学
DNA
遗传学
辐照
细胞
物理
核物理学
作者
Ruqun Wu,Wenjing Liu,Yujie Sun,C. Shen,Jinlong Guo,Jing Zhao,Guangbo Mao,Yaning Li,Guanghua Du
出处
期刊:DNA Repair
[Elsevier]
日期:2020-09-19
卷期号:96: 102974-102974
被引量:5
标识
DOI:10.1016/j.dnarep.2020.102974
摘要
The dynamic structure of nuclear chromatin and its regulation in the formation of repair complex is essential in DNA damage response and repair. Using single molecule localization microscopy STORM this work discovered that the nuclear chromatin organization was relaxed from 200 to 400 nm thick irregular frame and remodeled to dispersed sub-100 nm structure in HeLa cells after X-ray irradiation. The DSB repair factors (γ-H2AX, MDC1, 53BP1) showed distribution as microscale-colocalized and nanoscale interlaced substructure in the DSB repair complex. The dual-color nanoscopic imaging of γ-H2AX and chromatin at the DSB sites suggest that DNA damage response and repair cascade are chromatin structure-dependent and also partly dependent on the distance to the DSB sites. The sub-100 nm structure of fibers and nanoclusters of the relaxed nuclear chromatin and the DSB repair factors highly resembled the cross-section view of chromatin organization. These data demonstrated the polymorphic and dynamic behavior of the chromatin organization in vivo, and provided nanoscale insight into the interplay between chromatin remodeling and DNA damage response and DNA repair.
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