Laboratory of Mammalian Molecular Embryology, Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK.
Medical Research Council (MRC) Metabolic Diseases Unit, Wellcome-MRC Institute of Metabolic Science-Metabolic Research Laboratories, Addenbrooke's Hospital, University of Cambridge, Cambridge CB2 0QQ, UK.
Cell Rep. 2023 Feb 28;42(2):112023. doi: 10.1016/j.celrep.2023.112023. Epub 2023 Jan 31.
At the moment of union in fertilization, sperm and oocyte are transcriptionally silent. The ensuing onset of embryonic transcription (embryonic genome activation [EGA]) is critical for development, yet its timing and profile remain elusive in any vertebrate species. We here dissect transcription during EGA by high-resolution single-cell RNA sequencing of precisely synchronized mouse one-cell embryos. This reveals a program of embryonic gene expression (immediate EGA [iEGA]) initiating within 4 h of fertilization. Expression during iEGA produces canonically spliced transcripts, occurs substantially from the maternal genome, and is mostly downregulated at the two-cell stage. Transcribed genes predict regulation by transcription factors (TFs) associated with cancer, including c-Myc. Blocking c-Myc or other predicted regulatory TF activities disrupts iEGA and induces acute developmental arrest. These findings illuminate intracellular mechanisms that regulate the onset of mammalian development and hold promise for the study of cancer.
在受精过程中,精子和卵子处于转录沉默状态。随后的胚胎转录(胚胎基因组激活[EGA])对于发育至关重要,但在任何脊椎动物物种中,其时间和特征仍然难以捉摸。我们在这里通过对精确同步的小鼠单细胞胚胎进行高分辨率单细胞 RNA 测序来解析 EGA 期间的转录。这揭示了一个胚胎基因表达程序(即早期 EGA[iEGA]),它在受精后 4 小时内开始。iEGA 期间的表达产生规范剪接的转录本,主要来自母本基因组,并在二细胞阶段大部分下调。转录基因预测受到与癌症相关的转录因子(TFs)的调节,包括 c-Myc。阻断 c-Myc 或其他预测的调节 TF 活性会破坏 iEGA 并诱导急性发育停滞。这些发现阐明了调节哺乳动物发育开始的细胞内机制,并为癌症研究提供了希望。