Kurimasa A, Nagata Y, Shimizu M, Emi M, Nakamura Y, Oshimura M
Department of Molecular and Cell Genetics, School of Life Science, Faculty of Medicine, Tottori University, Japan.
Hum Genet. 1994 Jan;93(1):21-6. doi: 10.1007/BF00218907.
In order to map the gene that is responsible for the DNA-repair defect in severe combined immune deficient (SCID) mice, a mixture of microcells independently isolated from mouse A9 cells containing pSV2neo-tagged human chromosomes 5, 7, 8, 9, 11, 15, 18 or 20 were fused with SCID fibroblast cell lines SCVA2 and SCVA4, which were originally established from lung tissue of the C.B.17-scid/scid mouse by SV40 virus transfection. After irradiation with 60Co gamma-rays and selection with antibiotic G418, 12 independent clones were obtained, of which 4 contained an intact chromosome 8, 3 clones contained a deleted chromosome 8 [del(8)q22-->qter or del(8)q23--> qter] and remaining 5 had no detectable or specific human chromosome. We further independently transferred a single human chromosome 8 or 11 into the SCVA cells via microcell fusion, and examined the radiation sensitivity of the microcell hybrids. Complementation of the radiation sensitivity was correlated with the presence of human chromosome 8 in microcell hybrids, whereas no correlation was observed in clones following the transfer of human chromosome 11. Thus, the results indicate that human chromosome 8 restored high sensitivity to ionizing radiation. A number of subclones that were radiation resistant or sensitive were isolated from the microcell hybrids. The concordance of the radiation sensitivity with the presence or absence of specific DNA fragments on chromosome 8 indicates that the human gene is located on the centromeric region of chromosome 8, i.e., 8p11.1--> q11.1.
为了定位导致严重联合免疫缺陷(SCID)小鼠DNA修复缺陷的基因,从含有pSV2neo标记的人类5号、7号、8号、9号、11号、15号、18号或20号染色体的小鼠A9细胞中独立分离出的微细胞混合物,与SCID成纤维细胞系SCVA2和SCVA4融合,这两个细胞系最初是通过SV40病毒转染从C.B.17-scid/scid小鼠的肺组织建立的。经60Coγ射线照射并用抗生素G418筛选后,获得了12个独立克隆,其中4个含有完整的8号染色体,3个克隆含有缺失的8号染色体[del(8)q22→qter或del(8)q23→qter],其余5个未检测到或未发现特定的人类染色体。我们进一步通过微细胞融合将单个人类8号或11号染色体独立导入SCVA细胞,并检测微细胞杂种的辐射敏感性。辐射敏感性的互补与微细胞杂种中人类8号染色体的存在相关,而在导入人类11号染色体后的克隆中未观察到相关性。因此,结果表明人类8号染色体恢复了对电离辐射的高敏感性。从微细胞杂种中分离出了一些抗辐射或辐射敏感的亚克隆。辐射敏感性与8号染色体上特定DNA片段的存在与否的一致性表明,人类基因位于8号染色体的着丝粒区域,即8p11.1→q11.1。