Gossen J A, Martus H J, Wei J Y, Vijg J
Molecular Genetics Section, Gerontology Division, Beth Israel Hospital, Boston, MA 02215, USA.
Mutat Res. 1995 Sep;331(1):89-97. doi: 10.1016/0027-5107(95)00055-n.
Transgenic mouse mutation models carrying bacterial marker genes in bacteriophage lambda shuttle vectors have been applied to study spontaneous or induced mutations in vivo. However, due to the nature of the shuttle vector these models are insensitive to large deletions. Clastogenic agents, which predominantly induce large deletions, were therefore found to yield very low responses in these assays. Here we report the use of LacZ plasmid-based transgenic mice, allowing the detection of a broad spectrum of mutations. Treatment of mice with X-rays (5 x 50 rads) resulted in induction of up to about 5-fold higher mutation frequencies in lung, spleen and liver. Analysis of spontaneous and induced mutant LacZ genes indicated that at least 40-50% of all mutations were caused by deletions. The possibility of detecting a broad spectrum of mutations with this system suggests that the LacZ plasmid-based transgenic mouse may be the mammalian model of choice for studying spontaneous and induced mutations in vivo.
携带噬菌体λ穿梭载体中细菌标记基因的转基因小鼠突变模型已被用于研究体内自发或诱导的突变。然而,由于穿梭载体的性质,这些模型对大的缺失不敏感。因此,主要诱导大缺失的致断裂剂在这些试验中显示出非常低的反应。在此,我们报告基于LacZ质粒的转基因小鼠的使用,其能够检测广泛的突变。用X射线(5×50拉德)处理小鼠导致肺、脾和肝中的突变频率诱导增加高达约5倍。对自发和诱导的突变LacZ基因的分析表明,所有突变中至少40 - 50%是由缺失引起的。用该系统检测广泛突变的可能性表明,基于LacZ质粒的转基因小鼠可能是研究体内自发和诱导突变的首选哺乳动物模型。