Hickson I D, Davies S L, Davies S M, Robson C N
Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, UK.
Int J Radiat Biol. 1990 Oct;58(4):561-8. doi: 10.1080/09553009014551921.
Mutants are invaluable in the study of DNA repair processes. The past 10 years have seen a rapid proliferation of papers describing the isolation of mammalian cell mutants exhibiting DNA repair abnormalities. A variety of DNA-damaging agents, including radiation, alkylating agents and bleomycin, have been used to select mutants. This mini-review will concentrate on radiation (particularly ionizing radiation)-sensitive mutants, whether selected directly on the basis of radiation sensitivity or subsequently found to be cross-sensitive to radiation. Commonly observed DNA repair defects are associated with sensitivity to radiation. For UV-sensitive mutants a defect in the incision step of excision repair is frequently seen. For ionizing radiation-sensitive mutants, the common feature is a defect in the repair of DNA strand breaks. This may take the form of a reduced rate of strand-break rejoining or of a lowering in the fidelity of rejoining. Recent work suggests that the DNA topoisomerases may participate in the repair of DNA strand breaks and that strand breaks induced by both topoisomerase inhibitory drugs and radiation may be repaired by common pathways.
突变体在DNA修复过程的研究中具有重要价值。在过去十年里,描述分离出表现出DNA修复异常的哺乳动物细胞突变体的论文迅速增多。包括辐射、烷化剂和博来霉素在内的多种DNA损伤剂已被用于筛选突变体。这篇小型综述将聚焦于对辐射(尤其是电离辐射)敏感的突变体,无论这些突变体是基于辐射敏感性直接筛选出来的,还是后来发现对辐射具有交叉敏感性的。常见的DNA修复缺陷与对辐射的敏感性相关。对于对紫外线敏感的突变体,经常会观察到切除修复的切口步骤存在缺陷。对于对电离辐射敏感的突变体,其共同特征是在DNA链断裂的修复方面存在缺陷。这可能表现为链断裂重新连接的速率降低,或者重新连接的保真度下降。最近的研究表明,DNA拓扑异构酶可能参与DNA链断裂的修复,并且由拓扑异构酶抑制药物和辐射诱导的链断裂可能通过共同途径进行修复。