Natarajan A T, Darroudi F, Jha A N, Meijers M, Zdzienicka M Z
MGC-Department of Radiation Genetics, Sylvius Laboratories, State University of Leiden, The Netherlands.
Mutat Res. 1993 May;299(3-4):297-303. doi: 10.1016/0165-1218(93)90106-n.
Several radiosensitive mutant cell lines of CHO and V79 cells have been studied to explore a possible correlation between radiation induced DNA lesions and chromosomal aberrations. In the xrs mutants which are deficient in DNA double strand break (DSB) repair, there is a correlation between the extent of the defect in repair and the frequencies of radiation induced chromosomal aberrations. In another type of radiosensitive mutant (V-C4), which has no detectable defect in DNA DSB repair, the frequencies of X-ray induced aberrations are high in comparison to wild type V79 cells. However, following treatment with restriction endonucleases or fission neutrons, the frequencies of aberrations are similar to those in V79, indicating that V-C4 cells are defective in repair of X-ray induced lesions other than DSBs. Though DSBs are the most important lesions leading to chromosomal aberrations, in repair deficient mutants, radiation induced lesions other than DSBs can lead to chromosomal aberrations.
已经对几种CHO和V79细胞的辐射敏感突变细胞系进行了研究,以探索辐射诱导的DNA损伤与染色体畸变之间可能存在的相关性。在缺乏DNA双链断裂(DSB)修复能力的xrs突变体中,修复缺陷的程度与辐射诱导的染色体畸变频率之间存在相关性。在另一种类型的辐射敏感突变体(V-C4)中,DNA DSB修复未检测到缺陷,与野生型V79细胞相比,X射线诱导的畸变频率较高。然而,在用限制性内切酶或裂变中子处理后,畸变频率与V79中的相似,表明V-C4细胞在修复除DSB之外的X射线诱导损伤方面存在缺陷。尽管DSB是导致染色体畸变的最重要损伤,但在修复缺陷的突变体中,除DSB之外的辐射诱导损伤也可导致染色体畸变。