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H3K4 Methylation-Dependent Memory of Somatic Cell Identity Inhibits Reprogramming and Development of Nuclear Transfer Embryos

机译:H3K4甲基化依赖性记忆体细胞身份抑制核转移胚胎的重编程和发展

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摘要

Vertebrate eggs can induce the nuclear reprogramming of somatic cells to enable production of cloned animals. Nuclear reprogramming is relatively inefficient, and the development of the resultant embryos is frequently compromised, in part due to the inappropriate expression of genes previously active in the donor nucleus. Here, we identify H3K4 methylation as a major epigenetic roadblock that limits transcriptional reprogramming and efficient nuclear transfer (NT). Widespread expression of donor-cell-specific genes was observed in inappropriate cell types in NT embryos, limiting their developmental capacity. The expression of these genes in reprogrammed embryos arises from epigenetic memories of a previously active transcriptional state in donor cells that is characterized by high H3K4 methylation. Reducing H3K4 methylation had little effect on gene expression in donor cells, but it substantially improved transcriptional reprogramming and development of NT embryos. These results show that H3K4 methylation imposes a barrier to efficient nuclear reprogramming and suggest approaches for improving reprogramming strategies.
机译:脊椎动物蛋可以诱导体细胞的核重新编程,以实现克隆动物的生产。核重新编程是相对效率的,并且所得胚胎的发展经常受到损害,部分原因是由于在供体核中的基因的表达不恰当。在这里,我们将H3K4甲基化鉴定为主要的表观遗传障碍,限制转录重编程和有效的核转移(NT)。在NT胚胎中的不恰当细胞类型中观察到供体细胞特异性基因的广泛表达,限制其发育能力。这些基因在重编程的胚胎中的表达出现在供体细胞中先前有源转录状态的表观遗传存储器,其特征在于高H3K4甲基化。降低H3K4甲基化对供体细胞中的基因表达几乎没有影响,但它基本上改善了NT胚胎的转录重编程和发育。这些结果表明,H3K4甲基化对有效的核重编程和建议改善重编程策略的方法施加了障碍。

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