Stem Cell Epigenetics Laboratory, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, and Norwegian Center for Stem Cell Research, 0317 Oslo, Norway.
Dev Cell. 2011 Dec 13;21(6):993-1004. doi: 10.1016/j.devcel.2011.10.008. Epub 2011 Dec 1.
A hallmark of anamniote vertebrate development is a window of embryonic transcription-independent cell divisions before onset of zygotic genome activation (ZGA). Chromatin determinants of ZGA are unexplored; however, marking of developmental genes by modified histones in sperm suggests a predictive role of histone marks for ZGA. In zebrafish, pre-ZGA development for ten cell cycles provides an opportunity to examine whether genomic enrichment in modified histones is present before initiation of transcription. By profiling histone H3 trimethylation on all zebrafish promoters before and after ZGA, we demonstrate here an epigenetic prepatterning of developmental gene expression. This involves pre-ZGA marking of transcriptionally inactive genes involved in homeostatic and developmental regulation by permissive H3K4me3 with or without repressive H3K9me3 or H3K27me3. Our data suggest that histone modifications are instructive for the developmental gene expression program.
无脊椎动物胚胎发育的一个显著特点是在合子基因组激活 (ZGA) 之前有一段转录独立性细胞分裂的窗口期。ZGA 的染色质决定因素尚未被探索;然而,精子中组蛋白的修饰标志着发育基因,这表明组蛋白标记对于 ZGA 具有预测作用。在斑马鱼中,十个细胞周期的 ZGA 前发育为检查转录起始前是否存在组蛋白修饰的基因组富集提供了机会。通过在 ZGA 前后对所有斑马鱼启动子的组蛋白 H3 三甲基化进行分析,我们在此证明了发育基因表达的表观遗传预编程。这涉及到通过允许的 H3K4me3 对参与稳态和发育调节的转录不活跃基因进行预 ZGA 标记,而无需抑制性 H3K9me3 或 H3K27me3。我们的数据表明,组蛋白修饰对于发育基因表达程序具有指导作用。