Maroschik Belinda, Gürtler Anne, Krämer Anne, Rößler Ute, Gomolka Maria, Hornhardt Sabine, Mörtl Simone, Friedl Anna A
Department of Radiation Oncology, Ludwig-Maximilians-University, Munich, Germany.
Radiat Oncol. 2014 Jan 9;9:15. doi: 10.1186/1748-717X-9-15.
Radiation-induced alterations in posttranslational histone modifications (PTMs) may affect the cellular response to radiation damage in the DNA. If not reverted appropriately, altered PTM patterns may cause long-term alterations in gene expression regulation and thus lead to cancer. It is therefore important to characterize radiation-induced alterations in PTM patterns and the factors affecting them.
A lymphoblastoid cell line established from a normal donor was used to screen for alterations in methylation levels at H3K4, H3K9, H3K27, and H4K20, as well as acetylation at H3K9, H3K56, H4K5, and H4K16, by quantitative Western Blot analysis at 15 min, 1 h and 24 h after irradiation with 2 Gy and 10 Gy. The variability of alterations in acetylation marks was in addition investigated in a panel of lymphoblastoid cell lines with differing radiosensitivity established from lung cancer patients.
The screening procedure demonstrated consistent hypomethylation at H3K4me3 and hypoacetylation at all acetylation marks tested. In the panel of lymphoblastoid cell lines, however, a high degree of inter-individual variability became apparent. Radiosensitive cell lines showed more pronounced and longer lasting H4K16 hypoacetylation than radioresistant lines, which correlates with higher levels of residual γ-H2AX foci after 24 h.
So far, the factors affecting extent and duration of radiation-induced histone alterations are poorly defined. The present work hints at a high degree of inter-individual variability and a potential correlation of DNA damage repair capacity and alterations in PTM levels.
辐射诱导的翻译后组蛋白修饰(PTM)改变可能影响细胞对DNA辐射损伤的反应。如果不能适当地恢复,改变的PTM模式可能导致基因表达调控的长期改变,从而引发癌症。因此,表征辐射诱导的PTM模式改变及其影响因素很重要。
使用从正常供体建立的淋巴母细胞系,通过定量蛋白质免疫印迹分析,在2 Gy和10 Gy照射后15分钟、1小时和24小时,筛选H3K4、H3K9、H3K27和H4K20的甲基化水平变化,以及H3K9、H3K56、H4K5和H4K16的乙酰化变化。此外,在一组从肺癌患者建立的具有不同放射敏感性的淋巴母细胞系中,研究了乙酰化标记变化的变异性。
筛选过程显示H3K4me3一致低甲基化,且所有测试的乙酰化标记均低乙酰化。然而,在淋巴母细胞系组中,个体间差异很大。放射敏感细胞系比放射抗性细胞系表现出更明显、更持久的H4K16低乙酰化,这与24小时后更高水平的残留γ-H2AX病灶相关。
到目前为止,影响辐射诱导组蛋白改变程度和持续时间的因素尚不清楚。目前的研究表明个体间差异很大,且DNA损伤修复能力与PTM水平改变之间可能存在相关性。