Imai H, Nakagama H, Komatsu K, Shiraishi T, Fukuda H, Sugimura T, Nagao M
Carcinogenesis, National Cancer Center Research Institute, 1-1, Tsukiji 5, Chuo-ku, Tokyo 104, Japan.
Proc Natl Acad Sci U S A. 1997 Sep 30;94(20):10817-20. doi: 10.1073/pnas.94.20.10817.
We have recently found that okadaic acid, which shows strong inhibitory activity on protein serine/threonine phosphatases and tumor-promoting activity in vivo and in vitro, induces minisatellite mutation (MSM). Human tumors and chemically induced counterparts in experimental animals are also sometimes associated with MSM. In the present study, we demonstrated minisatellite (MS) instability in severe combined immunodeficiency (SCID) cells in which the DNA-dependent protein kinase catalytic subunit (DNA-PKcs) is impaired. Cells from a SCID fibroblast cell line transformed by simian virus 40 large tumor antigen, SC3VA2, and from an embryonal SCID fibroblast cell line, SC1K, were cloned and propagated to 10(7) to 10(8) cells, and then subjected to subcloning. After propagation of each subclone to 10(7) to 10(8) cells, DNA samples were digested with HinfI and analyzed by Southern blotting using the Pc-1 MS sequence as a probe. Under low-stringency conditions, about 40 MS bands were detected, with 45% +/- 6% and 37% +/- 3% of SC3VA2 and SC1K cells, respectively, having MSM. In contrast, cells from the RD13B2 cell line, which was established from SCVA2 by introducing human chromosome 8q fragments, on which DNA-PKcs is known to reside, to complement the SCID phenotype, showed a very low frequency of MSM (3% +/- 3%). The high frequencies of MSM in SC3VA2 and SC1K were significant, with no difference between the two. The present study clearly demonstrates that MS instability exists in SCID fibroblasts, suggesting that DNA-PKcs might be involved in the stable maintenance of MS sequences in the genome.
我们最近发现,冈田酸对蛋白质丝氨酸/苏氨酸磷酸酶具有强烈的抑制活性,并且在体内和体外均具有促肿瘤活性,它可诱导微卫星突变(MSM)。人类肿瘤以及实验动物中化学诱导产生的肿瘤有时也与MSM有关。在本研究中,我们证明了严重联合免疫缺陷(SCID)细胞中存在微卫星(MS)不稳定性,其中DNA依赖性蛋白激酶催化亚基(DNA-PKcs)受损。将经猿猴病毒40大肿瘤抗原转化的SCID成纤维细胞系SC3VA2以及胚胎SCID成纤维细胞系SC1K的细胞进行克隆,并扩增至10⁷至10⁸个细胞,然后进行亚克隆。将每个亚克隆扩增至10⁷至10⁸个细胞后,用HinfI消化DNA样本,并使用Pc-1 MS序列作为探针通过Southern印迹法进行分析。在低严谨条件下,检测到约40条MS条带,SC3VA2和SC1K细胞中分别有45%±6%和37%±3%发生了MSM。相比之下,通过导入已知含有DNA-PKcs的人类染色体8q片段以补充SCID表型而从SCVA2建立的RD13B2细胞系的细胞,其MSM频率非常低(3%±3%)。SC3VA2和SC1K中MSM的高频率具有显著性,两者之间无差异。本研究清楚地表明SCID成纤维细胞中存在MS不稳定性,这表明DNA-PKcs可能参与了基因组中MS序列的稳定维持。