Valdivia R P, Kunieda T, Azuma S, Toyoda Y
Department of Animal Pathology, University of Tokyo, Japan.
Mol Reprod Dev. 1993 Jun;35(2):121-6. doi: 10.1002/mrd.1080350204.
A two-step polymerase chain reaction (PCR) assay was used to determine the sex of mouse preimplantation embryos obtained from oocytes fertilized and cultured in vitro, to investigate the differences in the developmental rates of mouse embryos according to the sex. All the in vitro developed embryos could be analyzed by this method. When the embryos were classified according to the time of morula to blastocyst transition as fast-intermediate- and slow-growing embryos, a significantly high percentage (78.0%) of the fast-developing embryos were identified as males; while a significantly lower percentage (42.5%) of slow-developing embryos were identified as males. The intermediate-developing embryos presented a sex ratio not significantly different from the total (57.5%). The deviation of sex ratio was further confirmed by embryo transfer experiment, where fast- and slow-developing embryos gave 76.2% and 25.7% male fetuses, respectively. We concluded that male mouse embryos fertilized and cultured in vitro develop faster than female embryos.
采用两步聚合酶链反应(PCR)分析法来确定从体外受精和培养的卵母细胞中获得的小鼠植入前胚胎的性别,以研究小鼠胚胎发育速率根据性别的差异。所有体外发育的胚胎都可以用这种方法进行分析。当根据桑椹胚向囊胚转变的时间将胚胎分为快速发育、中等发育和缓慢发育的胚胎时,快速发育的胚胎中被鉴定为雄性的比例显著较高(78.0%);而缓慢发育的胚胎中被鉴定为雄性的比例显著较低(42.5%)。中等发育的胚胎呈现出与总体性别比例无显著差异的性别比例(57.5%)。胚胎移植实验进一步证实了性别比例的偏差,其中快速发育和缓慢发育的胚胎分别产生了76.2%和25.7%的雄性胎儿。我们得出结论,体外受精和培养的雄性小鼠胚胎比雌性胚胎发育得更快。