Worrad D M, Ram P T, Schultz R M
Department of Biology, University of Pennsylvania, Philadelphia 19104-6018.
Development. 1994 Aug;120(8):2347-57. doi: 10.1242/dev.120.8.2347.
We previously demonstrated that an Sp1-dependent reporter gene is preferentially expressed in G2 of the 1-cell mouse embryo following microinjection of the male pronucleus when compared to microinjection of the female pronucleus (P.T. Ram and R.M. Schultz, 1993, Dev. Biol. 156, 552-556). We also noted that expression of the reporter gene is not observed following microinjection of the germinal vesicle of the fully grown oocyte. In the present study, we examined expression of this reporter gene during oocyte growth, as well as the nuclear concentration of two transcription factors, Sp1 and the TATA box-binding protein, TBP, during oocyte growth and the first cell cycle. The extent of reporter gene expression decreases during oocyte growth and this decrease correlates with the decrease in nuclear concentration of Sp1, as determined by confocal immunofluorescent microscopy. In addition, results of immunoblotting experiments also indicate a similar decrease in the total concentration of Sp1 during oocyte growth. The nuclear concentration of TBP also decreases during oocyte growth, as determined by confocal immunofluorescent microscopy. Following fertilization, the pronuclear concentration of these two transcription factors increases in a time-dependent fashion and the concentration of each is greater in the male pronucleus as compared to the female pronucleus. For each pronucleus and for each transcription factor, this increase in nuclear concentration is inhibited by aphidicolin, which inhibits DNA synthesis. Last, the increase in nuclear concentration of these two proteins observed between the 1-cell and 2-cell stages does not require transcription or cytokinesis.
我们先前证明,与向雌性原核显微注射相比,向雄性原核显微注射后,一个依赖Sp1的报告基因在单细胞小鼠胚胎的G2期优先表达(P.T. 拉姆和R.M. 舒尔茨,1993年,《发育生物学》156卷,552 - 556页)。我们还注意到,向完全成熟卵母细胞的生发泡显微注射后未观察到报告基因的表达。在本研究中,我们检测了该报告基因在卵母细胞生长过程中的表达,以及两种转录因子Sp1和TATA盒结合蛋白TBP在卵母细胞生长和第一个细胞周期中的核浓度。通过共聚焦免疫荧光显微镜测定,报告基因表达程度在卵母细胞生长过程中降低,且这种降低与Sp1核浓度的降低相关。此外,免疫印迹实验结果也表明卵母细胞生长过程中Sp1总浓度有类似降低。通过共聚焦免疫荧光显微镜测定,TBP的核浓度在卵母细胞生长过程中也降低。受精后,这两种转录因子的原核浓度以时间依赖方式增加,且每个因子在雄性原核中的浓度高于雌性原核。对于每个原核和每种转录因子,这种核浓度的增加被抑制DNA合成的阿非科林所抑制。最后,在单细胞和二细胞阶段之间观察到的这两种蛋白质核浓度的增加不需要转录或胞质分裂。