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The Effect of Activation of Mammalian Oocytes on Remodeling of Donor Nuclei after Nuclear Transfer

生物 离子霉素 卵母细胞激活 环己酰亚胺 细胞生物学 胚泡 分子生物学 胚胎 促成熟因子 合子 体细胞 体细胞核移植 细胞周期 卵母细胞 细胞周期蛋白 胚胎发生 遗传学 细胞 蛋白质生物合成 基因 细胞内
作者
Jan Motlík,Ramiro Alberio,Valeri Zakhartchenko,Miodrag Stojković,Michal Kubelka,Eckhard Wolf
出处
期刊:Cloning and Stem Cells [Mary Ann Liebert, Inc.]
卷期号:4 (3): 245-252 被引量:11
标识
DOI:10.1089/15362300260339520
摘要

Activation of bovine oocytes by experimental procedures that closely mimic normal fertilization is essential both for intracytoplasmic sperm injection and for nuclear transfer (NT). Therefore, with the goal of producing haploid activated oocytes, we evaluated whether butyrolactone I and bohemine, either alone or in combination with ionomycin, are able to activate young matured mammalian oocytes. Furthermore, the effect on the patterns of DNA synthesis after pronuclear formation as well as changes in histone H1 kinase and MAP kinase activities during the process of activation were studied. Our results with bohemine show that the specific inhibition of cyclin-dependent kinases (CDKs) in metaphase II bovine oocytes induces parthenogenetic activation in a dose dependent manner (25, 50, and 100 microM, respectively), either alone (3%, 30%, and 50%) or in combination with ionomycin (30%, 70%, and 87.5%). The effect of two activation protocols on nuclear remodeling, DNA synthesis during the first cell cycle, chromosome segregation after first mitosis, and development to blastocyst of embryos produced by somatic nuclear transfer were studied. Pronuclear formation was significantly higher when activation lasted 5 h compared to 3 h for both ethanol-cycloheximide and ionomycin-bohemine treatment. Initiation of DNA synthesis was delayed in ethanol-cycloheximide group, however, after 12-h labeling 100% of embryos synthesized DNA in both groups. Analysis of two-cell embryos with DNA probes for chromosome 6, 7, and 15 by fluorescence in situ hybridization showed that at least 50% of NT embryos were of normal ploidy, independent of the activation protocol.
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