M. Smoluchowski Institute of Physics, Jagiellonian University, Łojasiewicza 11, 30-348 Kraków, Poland.
Int J Mol Sci. 2022 Mar 24;23(7):3524. doi: 10.3390/ijms23073524.
Even several thousands of DNA lesions are induced in one cell within one day. DNA damage may lead to mutations, formation of chromosomal aberrations, or cellular death. A particularly cytotoxic type of DNA damage is single- and double-strand breaks (SSBs and DSBs, respectively). In this work, we followed DNA conformational transitions induced by the disruption of DNA backbone. Conformational changes of chromatin in living cells were induced by a bleomycin (BLM), an anticancer drug, which generates SSBs and DSBs. Raman micro-spectroscopy enabled to observe chemical changes at the level of single cell and to collect hyperspectral images of molecular structure and composition with sub-micrometer resolution. We applied multivariate data analysis methods to extract key information from registered data, particularly to probe DNA conformational changes. Applied methodology enabled to track conformational transition from B-DNA to A-DNA upon cellular response to BLM treatment. Additionally, increased expression of proteins within the cell nucleus resulting from the activation of repair processes was demonstrated. The ongoing DNA repair process under the BLM action was also confirmed with confocal laser scanning fluorescent microscopy.
即使在一天内,一个细胞中也会产生数千个 DNA 损伤。DNA 损伤可能导致突变、染色体畸变或细胞死亡。一种特别细胞毒性的 DNA 损伤是单链和双链断裂(分别为 SSB 和 DSB)。在这项工作中,我们跟踪了由 DNA 骨架破坏引起的 DNA 构象转变。通过博来霉素(BLM),一种抗癌药物,诱导活细胞中染色质的构象变化,该药物会产生 SSB 和 DSB。拉曼微光谱能够观察到单细胞水平的化学变化,并以亚微米分辨率收集分子结构和组成的超光谱图像。我们应用多元数据分析方法从注册数据中提取关键信息,特别是探测 DNA 构象变化。应用的方法学能够在细胞对 BLM 处理的反应中从 B-DNA 跟踪到 A-DNA 的构象转变。此外,还证明了细胞内由于修复过程的激活而导致的核内蛋白质表达增加。还通过共聚焦激光扫描荧光显微镜证实了 BLM 作用下正在进行的 DNA 修复过程。