Institute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha 410078, China; Key Laboratory of Reproductive and Stem Cell Engineering, Ministry of Health, Changsha 410078, China; Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha 410078, China.
Center of System Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100005, China; Suzhou Institute of Systems Medicine, Suzhou 215123, China.
Cell Stem Cell. 2019 Nov 7;25(5):697-712.e6. doi: 10.1016/j.stem.2019.09.004. Epub 2019 Oct 3.
To investigate the contribution of parental genomes to early embryogenesis, we profiled the single-cell transcriptomes of human biparental and uniparental embryos systematically from the 1-cell to the morula stage. We observed that uniparental embryos exhibited variable and decreased embryonic genome activation (EGA). Comparative transcriptome analysis identified 807 maternally biased expressed genes (MBGs) and 581 paternally biased expressed genes (PBGs) in the preimplantation stages. MBGs became apparent at the 4-cell stage and contributed to the initiation of EGA, whereas PBGs preferentially appeared at the 8-cell stage and might affect embryo compaction and trophectoderm specification. Regulatory network analysis revealed that DUX4, EGR2, and DUXA are key transcription factors in MBGs' expression; ZNF263 and KLF3 are important for PBGs' expression. We demonstrated that parent-specific DNA methylation might account for the expression of most PBGs. Our results provide a valuable resource to understand parental genome activation and might help to elucidate parent-of-origin effects in early human development.
为了探究双亲基因组对早期胚胎发生的贡献,我们系统地分析了人类双亲核和单亲核胚胎从单细胞到桑葚胚阶段的单细胞转录组。我们观察到,单亲核胚胎表现出可变的和降低的胚胎基因组激活(EGA)。比较转录组分析在植入前阶段鉴定出 807 个母源偏表达基因(MBGs)和 581 个父源偏表达基因(PBGs)。MBGs 在 4 细胞阶段明显出现,并有助于 EGA 的启动,而 PBGs 则优先在 8 细胞阶段出现,可能影响胚胎致密化和滋养外胚层的特化。调控网络分析表明,DUX4、EGR2 和 DUXA 是 MBGs 表达的关键转录因子;ZNF263 和 KLF3 对 PBGs 的表达很重要。我们证明了亲本特异性 DNA 甲基化可能解释了大多数 PBGs 的表达。我们的研究结果为理解双亲基因组的激活提供了有价值的资源,并可能有助于阐明早期人类发育中的亲本来源效应。