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Genome Transfer Prevents Fragmentation and Restores Developmental Potential of Developmentally Compromised Postovulatory Aged Mouse?Oocytes

机译:基因组转移防止碎片化并恢复发育受损的排卵后老年小鼠卵母细胞的发育潜能

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Summary Changes in oocyte quality can have great impact on the developmental potential of early embryos. Here we test whether nuclear genome transfer from a developmentally incompetent to a developmentally competent oocyte can restore developmental potential. Using in?vitro oocyte aging as a model system we performed nuclear transfer in mouse oocytes at metaphase {II} or at the first interphase, and observed that development to the blastocyst stage and to term was as efficient as in control embryos. The increased developmental potential is explained primarily by correction of abnormal cytokinesis at anaphase of meiosis and mitosis, by a reduction in chromosome segregation errors, and by normalization of the localization of chromosome passenger complex components survivin and cyclin B1. These observations demonstrate that developmental decline is primarily due to abnormal function of cytoplasmic factors involved in cytokinesis, while the genome remains developmentally fully competent.
机译:小结卵母细胞质量的变化会对早期胚胎的发育潜力产生重大影响。在这里,我们测试核基因组是否从发育不全的卵母细胞转移到发育合格的卵母细胞是否可以恢复发育潜能。使用体外卵母细胞衰老作为模型系统,我们在中期{II}或第一个中间期在小鼠卵母细胞中进行了核转移,并观察到发育到胚泡期和足月与对照胚胎一样有效。发育潜力的提高主要通过减数分裂和有丝分裂后期的异常细胞分裂纠正,染色体分离错误的减少以及染色体乘客复合物组件survivin和cyclin B1的定位正常化来解释。这些观察结果表明发育下降主要是由于参与胞质分裂的细胞质因子的功能异常,而基因组仍具有发育上的能力。

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