Chen Stefanie H, Byrne Rose T, Wood Elizabeth A, Cox Michael M
Department of Biochemistry, University of Wisconsin-Madison, Madison, WI 53706, USA.
Mol Microbiol. 2015 Mar;95(5):754-68. doi: 10.1111/mmi.12885. Epub 2015 Jan 16.
A transposon insertion screen implicated the yejH gene in the repair of ionizing radiation-induced damage. The yejH gene, which exhibits significant homology to the human transcription-coupled DNA repair gene XPB, is involved in the repair of double-strand DNA breaks. Deletion of yejH significantly sensitized cells to agents that cause double-strand breaks (ionizing radiation, UV radiation, ciprofloxacin). In addition, deletion of both yejH and radA hypersensitized the cells to ionizing radiation, UV and ciprofloxacin damage, indicating that these two genes have complementary repair functions. The ΔyejH ΔradA double deletion also showed a substantial decline in viability following an induced double-strand DNA break, of a magnitude comparable with the defect measured when the recA, recB, recG or priA genes are deleted. The ATPase activity and C-terminal zinc finger motif of yejH play an important role in its repair function, as targeted mutant alleles of yejH did not rescue sensitivity. We propose that yejH be renamed radD, reflecting its role in the DNA repair of radiation damage.
转座子插入筛选表明yejH基因参与电离辐射诱导损伤的修复。yejH基因与人类转录偶联DNA修复基因XPB具有显著同源性,参与双链DNA断裂的修复。缺失yejH会使细胞对导致双链断裂的试剂(电离辐射、紫外线辐射、环丙沙星)高度敏感。此外,同时缺失yejH和radA会使细胞对电离辐射、紫外线和环丙沙星损伤极度敏感,表明这两个基因具有互补的修复功能。ΔyejHΔradA双缺失在诱导双链DNA断裂后也显示出活力大幅下降,其程度与缺失recA、recB、recG或priA基因时测得的缺陷相当。yejH的ATPase活性和C端锌指基序在其修复功能中起重要作用,因为yejH的靶向突变等位基因无法挽救敏感性。我们建议将yejH重新命名为radD,以反映其在辐射损伤DNA修复中的作用。