Liu W, Lu G X
Human Reproductive Engineering Lab of Xiangya Medical College, Central South University, Changsha 410078, China.
Yi Chuan Xue Bao. 2001;28(9):827-31.
In situ fluorescence hybridization (FISH) was used to study the integration and localization of human APPSWE gene on chromosomes of transgenic mice. It was found that in 2 founder mice, 34 and 36 metaphases of 80 metaphases observed had shown obvious specific hybridizing signals, the detection rates were 42.5% and 45%, respectively; meanwhile, in 1 F1 and 1 F2 mice, 33 and 30 metaphases out of 100 metaphases observed had specific hybridizing signals, the detection rates were 33% and 30%, respectively. The transgenes were localized on chromosome 8, 1, 17 and 2. The results indicated that transgene APPSWE were integrated stably into the chromosomes of transgenic mice and could be transmitted to offsprings through germ cells. The transgenes were randomly integrated into multiple sites of mice chromosomes. Meanwhile, the phenotypes of transgenic mice were also studied and different integrated sites had obvious effects on the pheonotypes.
采用原位荧光杂交(FISH)技术研究人APPSWE基因在转基因小鼠染色体上的整合及定位情况。结果发现,在2只奠基小鼠中,观察的80个中期相中分别有34个和36个中期相呈现明显的特异性杂交信号,检出率分别为42.5%和45%;同时,在1只F1小鼠和1只F2小鼠中,观察的100个中期相中分别有33个和30个中期相出现特异性杂交信号,检出率分别为33%和30%。转基因定位于8号、1号、17号和2号染色体上。结果表明,转基因APPSWE已稳定整合到转基因小鼠的染色体中,并可通过生殖细胞传递给后代。转基因随机整合到小鼠染色体的多个位点。同时,对转基因小鼠的表型也进行了研究,不同的整合位点对表型有明显影响。