Danish Center of Molecular Gerontology and Danish Aging Research Center, Department of Molecular Biology and Genetics, University of Aarhus, Denmark.
Environ Mol Mutagen. 2013 Jul;54(6):414-20. doi: 10.1002/em.21791. Epub 2013 Jun 25.
Accumulation of DNA damage deriving from exogenous and endogenous sources has significant consequences for cellular survival, and is implicated in aging, cancer, and neurological diseases. Different DNA repair pathways have evolved in order to maintain genomic stability. Genetic and environmental factors are likely to influence DNA repair capacity. In order to gain more insight into the genetic and environmental contribution to the molecular basis of DNA repair, we have performed a human twin study, where we focused on the consequences of some of the most abundant types of DNA damage (single-strand breaks), and some of the most hazardous lesions (DNA double-strand breaks). DNA damage signaling response (Gamma-H2AX signaling), relative amount of endogenous damage, and DNA-strand break repair capacities were studied in peripheral blood mononuclear cells from 198 twins (94 monozygotic and 104 dizygotic). We did not detect genetic effects on the DNA-strand break variables in our study.
外源和内源性来源的 DNA 损伤的积累对细胞存活有重大影响,并与衰老、癌症和神经退行性疾病有关。为了维持基因组稳定性,已经进化出不同的 DNA 修复途径。遗传和环境因素可能会影响 DNA 修复能力。为了更深入地了解遗传和环境因素对 DNA 修复分子基础的贡献,我们进行了一项人类双胞胎研究,其中我们关注了一些最丰富的 DNA 损伤类型(单链断裂)和一些最危险的损伤(双链 DNA 断裂)的后果。我们研究了来自 198 对双胞胎(94 对同卵双胞胎和 104 对异卵双胞胎)的外周血单核细胞中的 DNA 损伤信号反应(γ-H2AX 信号)、内源性损伤的相对量和 DNA 链断裂修复能力。在我们的研究中,我们没有检测到 DNA 链断裂变量的遗传效应。