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Nanoscale insight into chromatin remodeling and DNA repair complex in HeLa cells after ionizing radiation

机译:纳米级洞察染色体重塑和DNA修复在电离辐射后Hela细胞中的DNA修复复合物

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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 (gamma-H2AX, MDC1, 53BP1) showed distribution as microscale-colocalized and nanoscale interlaced substructure in the DSB repair complex. The dual-color nanoscopic imaging of gamma-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.
机译:核染色质的动态结构及其在修复复合物形成中的调节在DNA损伤反应和修复中至关重要。利用单分子定位显微镜,本研究发现,在X射线照射后,HeLa细胞的核染色质组织从200 nm厚的不规则框架松弛到400 nm厚,并重塑为分散的亚100 nm结构。DSB修复因子(γ-H2AX、MDC1、53BP1)在DSB修复复合体中以微尺度共定位和纳米尺度交错亚结构的形式分布。伽马-H2AX和染色质在DSB位点的双色纳米成像表明,DNA损伤反应和修复级联依赖于染色质结构,也部分依赖于到DSB位点的距离。松弛核染色质和DSB修复因子的纤维和纳米团簇的亚100nm结构与染色质组织的横截面图非常相似。这些数据证明了体内染色质组织的多态性和动态行为,并为染色质重塑、DNA损伤反应和DNA修复之间的相互作用提供了纳米级的见解。

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