Chen D J, Marrone B L, Nguyen T, Stackhouse M, Zhao Y, Siciliano M J
Life Sciences Division, Los Alamos National Laboratory, New Mexico 87545.
Genomics. 1994 May 15;21(2):423-7. doi: 10.1006/geno.1994.1287.
A number of human genes involved in the repair of radiation-induced DNA double-strand breaks have been identified based on the analysis of radiation-sensitive rodent mutants. Recently, one of the DSB repair genes, XRCC5, has been mapped on human chromosome 2 by concordance analysis of somatic cell hybrids and by the microcell-mediated chromosome transfer approach. For the regional mapping of the human XRCC5 gene, we have constructed a panel of X-ray hybrids and a panel of microcell-mediated chromosome 2 hybrids in the mutant background that contain only fragments of human chromosome 2. By using fluorescence in situ hybridization, chromosome banding, and physical mapping of these X-ray hybrids, we have localized the human XRCC5 locus to 2q35. This result is further confirmed by a segregation analysis indicating that the radiation resistant phenotype of a repair-proficient hybrid cosegregates with the human 2q35 chromosome fragment.
基于对辐射敏感的啮齿动物突变体的分析,已经鉴定出了一些参与修复辐射诱导的DNA双链断裂的人类基因。最近,通过体细胞杂种的一致性分析和微细胞介导的染色体转移方法,将其中一个DSB修复基因XRCC5定位到了人类2号染色体上。为了对人类XRCC5基因进行区域定位,我们构建了一组X射线杂种细胞系和一组在突变背景下仅包含人类2号染色体片段的微细胞介导的2号染色体杂种细胞系。通过对这些X射线杂种细胞系进行荧光原位杂交、染色体显带和物理图谱分析,我们将人类XRCC5基因座定位到了2q35。分离分析进一步证实了这一结果,表明修复功能正常的杂种细胞的抗辐射表型与人类2q35染色体片段共分离。