Brevini T A L, Lonergan P, Cillo F, Francisci C, Favetta L A, Fair T, Gandolfi F
Department of Anatomy of Domestic Animals, University of Milan, via Celoria, 10-20133 Milano, Italy.
Mol Reprod Dev. 2002 Dec;63(4):510-7. doi: 10.1002/mrd.10191.
In this study we analyzed the pattern of polyadenylation changes that takes place between the resumption of meiosis and the first cleavage of bovine oocytes. Moreover, we investigated whether the delayed occurrence of the first cleavage division, which characterizes embryos of low developmental competence, is accompanied by an altered polyadenylation pattern of individual transcripts. We determined the polyadenylation status of a group of genes that characterize physiological processes, involved in early differentiation (Oct-4), compaction, and cavitation (beta-actin, plakophilin, connexin-32, connexin-43), energy metabolism (glucose transporter type 1, pyruvate dehydrogenase phosphatase), RNA processing (RNA poly(A) polymerase), and stress (heat shock protein 70). RNA was isolated from pools of 20 oocytes or embryos at the germinal vesicle (GV) stage, at the end of in vitro maturation, at the end of in vitro fertilization, and at the time of the first cleavage. Cleavage was assessed 27, 30, 36, 42 hr post insemination (hpi), and at the latter time the remaining uncleaved oocytes were retained as a group. Between oocyte isolation and first cleavage at 27 hpi (best quality embryos), the poly(A) tail of individual transcripts followed four patterns: no changes (beta-actin, PDP); gradual reduction (Cx-43, Oct-4, Plako); gradual elongation (Cx-32, TPA); reduction followed by elongation (PAP, HSP-70, Glut-1). If the interval between insemination and first cleavage was longer than 27 hpi (progressively lower quality embryos) further changes of polyadenylation were observed, which differed for each gene considered. These data indicated that specific changes in polyadenylation contribute to the modulation of gene expression in bovine embryos at this stage of development. Defective developmental competence is accompanied by abnormal polyadenylation levels of specific maternal mRNAs with synchrony between polyadenylation and cleavage emerging as an apparently important factor.
在本研究中,我们分析了牛卵母细胞减数分裂恢复至第一次卵裂期间多聚腺苷酸化变化的模式。此外,我们研究了发育能力低的胚胎所特有的第一次卵裂延迟发生是否伴随着单个转录本多聚腺苷酸化模式的改变。我们确定了一组表征生理过程的基因的多聚腺苷酸化状态,这些生理过程涉及早期分化(Oct-4)、致密化和空泡化(β-肌动蛋白、桥粒斑蛋白、连接蛋白32、连接蛋白43)、能量代谢(1型葡萄糖转运蛋白、丙酮酸脱氢酶磷酸酶)、RNA加工(RNA多聚腺苷酸聚合酶)和应激(热休克蛋白70)。在生发泡(GV)期、体外成熟结束时、体外受精结束时以及第一次卵裂时,从20个卵母细胞或胚胎的样本中分离RNA。在授精后27、30、36、42小时(hpi)评估卵裂情况,在较晚时间,将剩余未卵裂的卵母细胞作为一组保留。在卵母细胞分离至27 hpi(质量最佳的胚胎)第一次卵裂期间,单个转录本的多聚腺苷酸尾呈现四种模式:无变化(β-肌动蛋白、丙酮酸脱氢酶磷酸酶);逐渐减少(连接蛋白43、Oct-4、桥粒斑蛋白);逐渐延长(连接蛋白32、组织型纤溶酶原激活剂);先减少后延长(多聚腺苷酸聚合酶、热休克蛋白70、葡萄糖转运蛋白1)。如果授精至第一次卵裂的间隔长于27 hpi(胚胎质量逐渐降低),则会观察到多聚腺苷酸化的进一步变化,每个所考虑的基因变化不同。这些数据表明,多聚腺苷酸化的特定变化有助于调节牛胚胎在这个发育阶段的基因表达。发育能力缺陷伴随着特定母源mRNA多聚腺苷酸化水平异常,多聚腺苷酸化与卵裂之间的同步性似乎是一个重要因素。