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Conversion of the Genetic Background of Transgenic Mice by In Vitro Fertilization

机译:通过体外受精转化转基因小鼠的遗传背景

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We attempted to convert the genetic background of transgenic (Tg) mice in a short period of time by applying in vitro fertilization techniques. Tg mice were obtained by injecting human interleukin-2 (hIL-2) gene into the fertilized eggs of the C57BL/6N strain. These Tg mice were back-crossed 8 times to the inbred C3H/HeN strain using the hIL-2 gene as the genetic selection marker. In order to shorten the length of the back-crossing time, in vitro fertilization was performed with eggs collected from immature Tg females and spermatozoa from mature C3H/HeN males, and successfully fertilized eggs (2-cell stage) were transferred to pseudopregnant recipients to obtain the offspring of next generation. When no offspring were obtained through the procedures using immature Tg females, in vitro fertilization was performed with mature Tg males and mature C3H/HeN females to continue successive back-crosses. With this method, it was possible to perform 8 successive back-crosses in 18 months.
机译:我们试图通过应用体外受精技术在短时间内转换转基因(Tg)小鼠的遗传背景。通过将人白介素2(hIL-2)基因注射到C57BL / 6N菌株的受精卵中来获得Tg小鼠。使用hIL-2基因作为遗传选择标记,将这些Tg小鼠与近交C3H / HeN株回交8次。为了缩短回交时间,对未成熟Tg雌性卵和成熟C3H / HeN雄性精子收集的卵进行体外受精,并将成功受精的卵(2细胞期)转移至假孕受者获得下一代的后代。当通过使用未成熟Tg雌性的程序未获得后代时,对成熟Tg雄性和成熟C3H / HeN雌性进行体外受精,以连续进行回交。使用此方法,有可能在18个月内执行8次连续回交。

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