Ricoul Michelle, Gnana Sekaran Tamizh Selvan, Brochard Patricia, Herate Cecile, Sabatier Laure
PROCyTox, French Alternative Energies and Atomic Energy Commission (CEA), Paris-Saclay University, 92260 Fontenay-aux-Roses, France.
Cancers (Basel). 2019 Sep 19;11(9):1397. doi: 10.3390/cancers11091397.
Many toxic agents can cause DNA double strand breaks (DSBs), which are in most cases quickly repaired by the cellular machinery. Using ionising radiation, we explored the kinetics of DNA lesion signaling and structural chromosome aberration formation at the intra- and inter-chromosomal level. Using a novel approach, the classic Premature Chromosome Condensation (PCC) was combined with γ-H2AX immunofluorescence staining in order to unravel the kinetics of DNA damage signalisation and chromosome repair. We identified an early mechanism of DNA DSB joining that occurs within the first three hours post-irradiation, when dicentric chromosomes and chromosome exchanges are formed. The slower and significant decrease of "deleted chromosomes" and 1 acentric telomere fragments observed until 24 h post-irradiation, leads to the conclusion that a second and error-free repair mechanism occurs. In parallel, we revealed remaining signalling of γ-H2AX foci at the site of chromosome fusion long after the chromosome rearrangement formation. Moreover there is important signalling of foci on the site of telomere and sub-telomere sequences suggesting either a different function of γ-H2AX signalling in these regions or an extreme sensibility of the telomere sequences to DNA damage that remains unrepaired 24 h post-irradiation. In conclusion, chromosome repair happens in two steps, including a last and hardly detectable one because of restoration of the chromosome integrity.
许多毒性因子可导致DNA双链断裂(DSB),在大多数情况下,细胞机制会迅速修复这些断裂。我们利用电离辐射,在染色体内部和染色体之间的水平上探究了DNA损伤信号传导和结构染色体畸变形成的动力学。采用一种新方法,将经典的早熟染色体凝集(PCC)与γ-H2AX免疫荧光染色相结合,以揭示DNA损伤信号传导和染色体修复的动力学。我们确定了一种DNA DSB连接的早期机制,该机制发生在照射后的前三小时内,此时会形成双着丝粒染色体和染色体交换。观察到直到照射后24小时“缺失染色体”和1个无着丝粒端粒片段才缓慢且显著减少,这导致我们得出结论,即发生了第二种无差错修复机制。与此同时,我们发现在染色体重排形成后很长时间,染色体融合部位仍有γ-H2AX焦点的残留信号。此外,端粒和亚端粒序列部位有重要的焦点信号,这表明γ-H2AX信号在这些区域可能具有不同功能,或者端粒序列对照射后24小时仍未修复的DNA损伤极度敏感。总之,染色体修复分两步进行,包括最后一步,由于染色体完整性的恢复,这一步很难检测到。