Yacoub A, Park J S, Qiao L, Dent P, Hagan M P
Department of Radiation Oncology, Medical College of Virginia, Virginia Commonwealth University, Richmond, VA 23298, USA.
Int J Radiat Biol. 2001 Oct;77(10):1067-78. doi: 10.1080/09553000110069317.
To examine the role of mitogen-activated protein kinase (MAPK) signalling on the induction by ionizing radiation of the nucleotide excision repair gene (ERCC1), the X-ray cross-complementing group 1 protein (XRCC1) and the repair of radiation-induced DNA damage.
The expression of ERCC1 and XRCC1 was examined in DU145 human prostate cancer cells following exposure to ionizing radiation. We characterized the MAPK dependence of this expression through RT-PCR analysis, Western analysis, transcription inhibition and measurement of the activation of each promoter. Pre-exposure with the specific MEK1/2 inhibitor PD980059 (10 microM) was used to blunt radiation induction of MAPK without suppressing basal levels of MAPK activity. In addition, we examined the MAPK dependence of DNA damage repair by measuring radiation-induced micronucleus formation and the removal of and nicking activity associated with AP sites.
Irradiation caused a time-dependent, MAPK-dependent increase in the protein levels of both ERCC1 and XRCC1. For each gene product, the protein level increase followed an increase in mRNA, which also was MAPK-dependent. Radiation also enhanced the activities of the ERCC1 and XRCC1 promoters in an MAPK-dependent fashion. Inhibition of transcription by DRB abolished the radiation-induced increase of ERCC1 and XRCC1 proteins. Inhibition of radiation-induced MAPK also diminished the ability of DU145 cells to remove AP sites and increased the number of cells displaying micronuclei following radiation exposure.
These findings demonstrate a role for radiation-induced MAPK signalling in the regulation of DNA repair enzyme levels and DNA repair. Radiation-induced protein expression of ERCC1 and XRCC1 appears to require de novo transcription. These data suggest a significant role for MAPK signalling in the early response to DNA damage caused by ionizing radiation.
研究丝裂原活化蛋白激酶(MAPK)信号通路在电离辐射诱导核苷酸切除修复基因(ERCC1)、X射线交叉互补组1蛋白(XRCC1)表达以及辐射诱导的DNA损伤修复中的作用。
检测DU145人前列腺癌细胞在暴露于电离辐射后ERCC1和XRCC1的表达。我们通过逆转录聚合酶链反应(RT-PCR)分析、蛋白质免疫印迹分析、转录抑制以及各启动子激活的测量来确定这种表达对MAPK的依赖性。用特异性MEK1/2抑制剂PD980059(10微摩尔)预暴露以抑制辐射诱导的MAPK,同时不抑制MAPK活性的基础水平。此外,我们通过测量辐射诱导的微核形成以及与AP位点相关的去除和切口活性来检测DNA损伤修复对MAPK的依赖性。
辐射导致ERCC1和XRCC1蛋白水平呈时间依赖性、MAPK依赖性增加。对于每个基因产物,蛋白水平的增加伴随着mRNA的增加,而mRNA的增加也是MAPK依赖性的。辐射还以MAPK依赖性方式增强了ERCC1和XRCC1启动子的活性。用5,6-二氯-1-β-D-呋喃核糖基苯并咪唑(DRB)抑制转录消除了辐射诱导的ERCC1和XRCC1蛋白增加。抑制辐射诱导的MAPK也降低了DU145细胞去除AP位点的能力,并增加了辐射暴露后显示微核的细胞数量。
这些发现证明了辐射诱导的MAPK信号通路在DNA修复酶水平调节和DNA修复中的作用。辐射诱导的ERCC1和XRCC1蛋白表达似乎需要从头转录。这些数据表明MAPK信号通路在对电离辐射引起的DNA损伤的早期反应中起重要作用。