Martin N T, Nakamura K, Paila U, Woo J, Brown C, Wright J A, Teraoka S N, Haghayegh S, McCurdy D, Schneider M, Hu H, Quinlan A R, Gatti R A, Concannon P
1] UCLA Department of Pathology and Laboratory Medicine, MacDonald Research Laboratories, Los Angeles, CA, USA [2] UCLA Biomedical Physics Interdepartmental Graduate Program, Los Angeles, CA, USA.
UCLA Department of Pathology and Laboratory Medicine, MacDonald Research Laboratories, Los Angeles, CA, USA.
Cell Death Dis. 2014 Mar 20;5(3):e1130. doi: 10.1038/cddis.2014.99.
The study of rare human syndromes characterized by radiosensitivity has been instrumental in identifying novel proteins and pathways involved in DNA damage responses to ionizing radiation. In the present study, a mutation in mitochondrial poly-A-polymerase (MTPAP), not previously recognized for its role in the DNA damage response, was identified by exome sequencing and subsequently associated with cellular radiosensitivity. Cell lines derived from two patients with the homozygous MTPAP missense mutation were radiosensitive, and this radiosensitivity could be abrogated by transfection of wild-type mtPAP cDNA into mtPAP-deficient cell lines. Further analysis of the cellular phenotype revealed delayed DNA repair, increased levels of DNA double-strand breaks, increased reactive oxygen species (ROS), and increased cell death after irradiation (IR). Pre-IR treatment of cells with the potent anti-oxidants, α-lipoic acid and n-acetylcysteine, was sufficient to abrogate the DNA repair and clonogenic survival defects. Our results firmly establish that mutation of the MTPAP gene results in a cellular phenotype of increased DNA damage, reduced repair kinetics, increased cell death by apoptosis, and reduced clonogenic survival after exposure to ionizing radiation, suggesting a pathogenesis that involves the disruption of ROS homeostasis.
对以放射敏感性为特征的罕见人类综合征的研究,在鉴定参与对电离辐射的DNA损伤反应的新蛋白质和信号通路方面发挥了重要作用。在本研究中,通过外显子组测序鉴定出线粒体多聚腺苷酸聚合酶(MTPAP)中的一种突变,该突变此前未被认识到在DNA损伤反应中的作用,随后发现其与细胞放射敏感性相关。来自两名携带纯合MTPAP错义突变患者的细胞系具有放射敏感性,将野生型mtPAP cDNA转染到mtPAP缺陷细胞系中可消除这种放射敏感性。对细胞表型的进一步分析显示,DNA修复延迟、DNA双链断裂水平增加、活性氧(ROS)增加以及照射后细胞死亡增加。用强效抗氧化剂α-硫辛酸和N-乙酰半胱氨酸对细胞进行照射前处理,足以消除DNA修复和克隆形成存活缺陷。我们的结果明确表明,MTPAP基因突变导致细胞出现DNA损伤增加、修复动力学减慢、细胞凋亡导致的细胞死亡增加以及暴露于电离辐射后克隆形成存活减少的表型,提示其发病机制涉及ROS稳态的破坏。