Yamamoto Satoshi, Nagao Yasumitsu, Kuroiwa Kenji, Hakamata Yoji, Ichida Masaru, Saito-Ohara Fumiko, Tominaga Kaoru, Endo Hitoshi
Department of Biochemistry, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke, Tochigi, 329-0498, Japan.
Transgenic Res. 2014 Oct;23(5):757-65. doi: 10.1007/s11248-014-9813-0. Epub 2014 Jul 10.
We developed a transgenic mouse line with Y chromosome-linked green fluorescent protein expressing transgenes (Y-GFP) by the conventional microinjection into the pronucleus of C57BL/6J fertilized oocytes. Embryonic stem (ES) cells derived from Y-GFP mice enabled not only sexing but also the identification of 39, XO karyotype by the lack of Y chromosome. Actually, when fluorescence activated cell sorting (FACS) was applied to Y-GFP ES cells, non-fluorescent ES cells were conveniently collected and showed the lack of Y chromosome by PCR genotyping and Southern blot analysis. FACS analysis revealed Y chromosome loss occurred at 2.9 % of 40, XY ES cells after five passages. These Y-GFP ES cells are potentially applicable to reduce the time, cost and effort needed to generate the gene-targeted mice by the production of male and female mice derived from the same ES cell clone.
我们通过将转基因显微注射到C57BL/6J受精卵的原核中,培育出了一种带有Y染色体连锁绿色荧光蛋白表达转基因(Y-GFP)的转基因小鼠品系。源自Y-GFP小鼠的胚胎干细胞(ES细胞)不仅能够进行性别鉴定,还能通过缺乏Y染色体来鉴定39,XO核型。实际上,当将荧光激活细胞分选(FACS)应用于Y-GFP ES细胞时,可方便地收集到无荧光的ES细胞,通过PCR基因分型和Southern印迹分析显示其缺乏Y染色体。FACS分析显示,经过5次传代后,40,XY ES细胞中有2.9%发生了Y染色体丢失。这些Y-GFP ES细胞有可能用于减少通过源自同一ES细胞克隆的雄性和雌性小鼠生产基因靶向小鼠所需的时间、成本和工作量。