Department of Radiation Oncology, University Hospital of Munich, Schillerstr. 42, 80336, Munich, Germany.
Chromosome Res. 2011 Oct;19(7):883-99. doi: 10.1007/s10577-011-9244-1. Epub 2011 Oct 11.
Epigenetic alterations induced by ionizing radiation may contribute to radiation carcinogenesis. To detect relative accumulations or losses of constitutive post-translational histone modifications in chromatin regions surrounding DNA double-strand breaks (DSB), we developed a method based on ion microirradiation and correlation of the signal intensities after immunofluorescence detection of the histone modification in question and the DSB marker γ-H2AX. We observed after ionizing irradiation markers for transcriptional silencing, such as accumulation of H3K27me3 and loss of active RNA polymerase II, at chromatin regions labeled by γ-H2AX. Confocal microscopy of whole nuclei and of ultrathin nuclear sections revealed that the histone modification H3K4me3, which labels transcriptionally active regions, is underrepresented in γ-H2AX foci. While some exclusion of H3K4me3 is already evident at the earliest time amenable to this kind of analysis, the anti-correlation apparently increases with time after irradiation, suggesting an active removal process. Focal accumulation of the H3K4me3 demethylase, JARID1A, was observed at damaged regions inflicted by laser irradiation, suggesting involvement of this enzyme in the DNA damage response. Since no accumulation of the repressive mark H3K9me2 was found at damaged sites, we suggest that DSB-induced transcriptional silencing resembles polycomb-mediated silencing rather than heterochromatic silencing.
电离辐射引起的表观遗传改变可能导致辐射致癌。为了检测 DNA 双链断裂(DSB)周围染色质区域中组成性翻译后组蛋白修饰的相对积累或丢失,我们开发了一种基于离子微照射的方法,并结合了所研究的组蛋白修饰和 DSB 标记 γ-H2AX 的免疫荧光检测后的信号强度的相关性。我们观察到电离照射后,在 γ-H2AX 标记的染色质区域中积累了转录沉默标记物,如 H3K27me3 和活性 RNA 聚合酶 II 的丢失。通过全核共焦显微镜和超薄核切片观察到,标记转录活性区域的组蛋白修饰 H3K4me3 在 γ-H2AX 焦点中代表性不足。虽然在这种分析最早可行的时间已经可以明显看出 H3K4me3 的排除,但显然随着照射后时间的推移,这种反相关增加,表明存在主动去除过程。在激光照射造成的损伤区域观察到 H3K4me3 去甲基化酶 JARID1A 的焦点积累,表明该酶参与了 DNA 损伤反应。由于在受损部位未发现抑制性标记物 H3K9me2 的积累,我们认为 DSB 诱导的转录沉默类似于多梳介导的沉默,而不是异染色质沉默。