Phillips E N, Xia F, Kelsey K T, Liber H L
Department of Cancer Biology, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
Radiat Res. 1995 Sep;143(3):255-62.
Previous work showed that WTK1 human lymphoblastoid cells are radioresistant but more sensitive to X-ray-induced mutation than the closely related line TK6. In addition, WTK1 cells contain a mutant p53 while in TK6 cells p53 is wild-type. In this work, we examined the spectra of 68 X-ray-induced and 56 spontaneous mutants at the hemizygous hprt locus in WTK1 cells. The induced spectra were classified by Southern blot and multiplex polymerase chain reaction (PCR); there were 19 point mutations (28%) with an unaltered Southern blot or PCR pattern, 26 (38%) partial deletions or rearrangements and 23 (34%) complete gene deletions. The spontaneous spectrum included 25 (45%) point mutations, 22 (39%) partial deletions and 9 (16%) complete gene deletions. These spectra of mutations were compared to those of TK6 cells. Although distinct differences in the spectra of mutations at the tk locus were reported previously, overall there is no significant difference in the spectra of X-ray-induced or spontaneous mutations at the hprt locus in these two cell lines. While there was an increase in the proportion of large-scale changes that occurred at tk after X irradiation, the spectrum of mutations at the hprt locus shows all classes of mutations increasing proportionately in WTK1 cells. However, the proportion of internal partial deletion mutations at the hprt locus was about 2 times more frequent in WTK1 than in TK6 cells.
先前的研究表明,WTK1人淋巴母细胞系具有辐射抗性,但与密切相关的TK6细胞系相比,对X射线诱导的突变更敏感。此外,WTK1细胞含有突变型p53,而TK6细胞中的p53是野生型。在本研究中,我们检测了WTK1细胞中半合子hprt位点的68个X射线诱导突变和56个自发突变的谱型。通过Southern印迹和多重聚合酶链反应(PCR)对诱导谱型进行分类;有19个点突变(28%),Southern印迹或PCR图谱未改变,26个(38%)部分缺失或重排,23个(34%)基因完全缺失。自发谱型包括25个(45%)点突变、22个(39%)部分缺失和9个(16%)基因完全缺失。将这些突变谱型与TK6细胞的进行比较。尽管先前报道了tk位点突变谱型存在明显差异,但总体而言,这两种细胞系中hprt位点的X射线诱导突变或自发突变谱型没有显著差异。虽然X射线照射后tk位点发生的大规模变化比例增加,但WTK1细胞中hprt位点的突变谱型显示所有类型的突变均成比例增加。然而,WTK1细胞中hprt位点内部部分缺失突变的比例比TK6细胞高约2倍。