Nestorov Peter, Hotz Hans-Rudolf, Liu Zichuan, Peters Antoine H F M
Friedrich Miescher Institute for Biomedical Research, 4058 Basel, Switzerland.
Faculty of Sciences, University of Basel, 4056 Basel, Switzerland.
Sci Rep. 2015 Sep 25;5:14347. doi: 10.1038/srep14347.
During mouse preimplantation development, major changes in cell fate are accompanied by extensive alterations of gene expression programs. Embryos first transition from a maternal to zygotic program and subsequently specify the pluripotent and the trophectodermal cell lineages. These processes are regulated by key transcription factors, likely in cooperation with chromatin modifiers that control histone and DNA methylation. To characterize the spatiotemporal expression of chromatin modifiers in relation to developmental transitions, we performed gene expression profiling of 156 genes in individual oocytes and single blastomeres of developing mouse embryos until the blastocyst stage. More than half of the chromatin modifiers displayed either maternal or zygotic expression. We also detected lineage-specific expression of several modifiers, including Ezh1, Prdm14, Scmh1 and Tet1 underscoring possible roles in cell fate decisions. Members of the SET-domain containing SMYD family showed differential gene expression during preimplantation development. We further observed co-expression of genes with opposing biochemical activities, such as histone methyltransferases and demethylases, suggesting the existence of a dynamic chromatin steady-state during preimplantation development.
在小鼠植入前发育过程中,细胞命运的重大变化伴随着基因表达程序的广泛改变。胚胎首先从母源程序过渡到合子程序,随后确定多能细胞和滋养外胚层细胞谱系。这些过程由关键转录因子调控,可能与控制组蛋白和DNA甲基化的染色质修饰因子协同作用。为了表征染色质修饰因子在发育转变过程中的时空表达,我们对发育至囊胚阶段的小鼠胚胎的单个卵母细胞和单个卵裂球中的156个基因进行了基因表达谱分析。超过一半的染色质修饰因子表现出母源或合子表达。我们还检测到几种修饰因子的谱系特异性表达,包括Ezh1、Prdm14、Scmh1和Tet1,这突出了它们在细胞命运决定中的可能作用。含SET结构域的SMYD家族成员在植入前发育过程中表现出差异基因表达。我们进一步观察到具有相反生化活性的基因,如组蛋白甲基转移酶和去甲基酶的共表达,这表明在植入前发育过程中存在动态染色质稳态。