Mtango Namdori R, Latham Keith E
The Fels Institute for Cancer Research and Molecular Biology, Temple University, Philadelphia, Pennsylvania 19140, USA.
Biol Reprod. 2008 Feb;78(2):254-66. doi: 10.1095/biolreprod.107.064931. Epub 2007 Oct 3.
Correct cell cycle regulation is especially challenging at the start of life. Ovulated oocytes must maintain meiotic arrest until fertilization, and then complete meiosis and initiate a series of modified cell divisions without growth. Moreover, myriad key developmental events, such as chromatin remodeling and transcriptional activation of the genome, are coordinated with each other via the cell cycle, particularly passage through the DNA synthesis phase (S Phase). We examined here the expression of more than 30 mRNAs related to cell cycle regulation in rhesus monkey oocytes and embryos and compared the expression of these mRNAs between oocytes and embryos of different developmental potentials. We find that the maternally inherited stores of cell cycle regulatory mRNAs are especially susceptible to disruption in cases of diminished oocyte and embryo quality in the rhesus monkey. In comparison to published mouse array data, we also observed striking species differences in the temporal expression patterns of many of these genes, suggesting that mechanisms of cell cycle control may differ and that the responses of oocytes and embryos to external insults may likewise differ.
正确的细胞周期调控在生命起始阶段尤其具有挑战性。排卵后的卵母细胞必须维持减数分裂停滞直至受精,然后完成减数分裂并启动一系列无生长的修饰细胞分裂。此外,众多关键的发育事件,如染色质重塑和基因组的转录激活,通过细胞周期相互协调,特别是在通过DNA合成期(S期)时。我们在此研究了恒河猴卵母细胞和胚胎中30多种与细胞周期调控相关的mRNA的表达,并比较了不同发育潜能的卵母细胞和胚胎之间这些mRNA的表达。我们发现,在恒河猴卵母细胞和胚胎质量下降的情况下,母系遗传的细胞周期调控mRNA储备特别容易受到破坏。与已发表的小鼠阵列数据相比,我们还观察到许多这些基因的时间表达模式存在显著的物种差异,这表明细胞周期控制机制可能不同,并且卵母细胞和胚胎对外部损伤的反应可能同样不同。