Balajee A S, Proietti De Santis L, Brosh R M, Selzer R, Bohr V A
Laboratory of Molecular Genetics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA.
Oncogene. 2000 Jan 27;19(4):477-89. doi: 10.1038/sj.onc.1203372.
Cockayne syndrome (CS) is a human autosomal recessive disorder characterized by many neurological and developmental abnormalities. CS cells are defective in the transcription coupled repair (TCR) pathway that removes DNA damage from the transcribed strand of active genes. The individuals suffering from CS do not generally develop cancer but show increased neurodegeneration. Two genetic complementation groups (CS-A and CS-B) have been identified. The lack of cancer formation in CS may be due to selective elimination of cells containing DNA damage by a suicidal pathway. In this study, we have evaluated the role of the CSB gene in UV induced apoptosis in human and hamster cells. The hamster cell line UV61 carries a mutation in the homolog of the human CSB gene. We show that both human CS-B and hamster UV61 cells display increased apoptotic response following UV exposure compared with normal cells. The increased sensitivity of UV61 cells to apoptosis is complemented by the transfection of the wild type human CSB gene. In order to determine which functional domain of the CSB gene participates in the apoptotic pathway, we constructed stable cell lines with different CSB domain disruptions. UV61 cells were stably transfected with the human CSB cDNA containing a point mutation in the highly conserved glutamic acid residue in ATPase motif II. This cell line (UV61/ pc3.1-CSBE646Q) showed the same increased apoptosis as the UV61 cells. In contrast, cells containing a deletion in the acidic domain at the N-terminal end of the CSB protein had no effect on apoptosis. This indicates that the integrity of the ATPase domain of CSB protein is critical for preventing the UV induced apoptotic pathway. In primary human CS-B cells, the induction and stabilization of the p53 protein seems to correlate with their increased apoptotic potential. In contrast, no change in the level of either p53 or activation of mdm2 protein by p53 was observed in hamster UV61 cells after UV exposure. This suggests that the CSB dependent apoptotic pathway can occur independently of the transactivation potential of p53 in hamster cells.
科凯恩综合征(CS)是一种常染色体隐性遗传病,其特征为多种神经和发育异常。CS细胞在转录偶联修复(TCR)途径中存在缺陷,该途径负责从活跃基因的转录链上去除DNA损伤。患有CS的个体通常不会患癌症,但会表现出神经退行性变增加。已鉴定出两个遗传互补组(CS-A和CS-B)。CS患者不患癌症可能是由于通过自杀途径选择性清除了含有DNA损伤的细胞。在本研究中,我们评估了CSB基因在紫外线诱导的人和仓鼠细胞凋亡中的作用。仓鼠细胞系UV61在人CSB基因的同源物中发生了突变。我们发现,与正常细胞相比,人CS-B细胞和仓鼠UV61细胞在紫外线照射后均表现出凋亡反应增加。野生型人CSB基因的转染可弥补UV61细胞对凋亡敏感性的增加。为了确定CSB基因的哪个功能域参与凋亡途径,我们构建了具有不同CSB结构域破坏的稳定细胞系。用在ATP酶基序II中高度保守的谷氨酸残基处含有点突变的人CSB cDNA稳定转染UV61细胞。该细胞系(UV61/ pc3.1-CSBE646Q)表现出与UV61细胞相同的凋亡增加。相反,CSB蛋白N末端酸性结构域缺失的细胞对凋亡没有影响。这表明CSB蛋白的ATP酶结构域的完整性对于阻止紫外线诱导的凋亡途径至关重要。在原代人CS-B细胞中,p53蛋白的诱导和稳定似乎与其增加的凋亡潜能相关。相反,紫外线照射后,在仓鼠UV61细胞中未观察到p53水平或p53对mdm2蛋白激活的变化。这表明CSB依赖性凋亡途径可以独立于仓鼠细胞中p53的反式激活潜能而发生。