生物
染色质
合子
重编程
细胞生物学
胚胎
舱室(船)
母子转换
遗传学
DNA甲基化
基因组
复制计时
胚胎发生
DNA
基因
基因表达
地质学
海洋学
作者
Yuwen Ke,Yanan Xu,Xuepeng Chen,Songjie Feng,Zhenbo Liu,Yaoyu Sun,Xuelong Yao,Fangzhen Li,Wei Zhu,Lei Gao,Haojie Chen,Zhenhai Du,Wei Xie,Xiaocui Xu,Xingxu Huang,Jiang Liu
出处
期刊:Cell
[Cell Press]
日期:2017-07-01
卷期号:170 (2): 367-381.e20
被引量:464
标识
DOI:10.1016/j.cell.2017.06.029
摘要
High-order chromatin structure plays important roles in gene expression regulation. Knowledge of the dynamics of 3D chromatin structures during mammalian embryo development remains limited. We report the 3D chromatin architecture of mouse gametes and early embryos using an optimized Hi-C method with low-cell samples. We find that mature oocytes at the metaphase II stage do not have topologically associated domains (TADs). In sperm, extra-long-range interactions (>4 Mb) and interchromosomal interactions occur frequently. The high-order structures of both the paternal and maternal genomes in zygotes and two-cell embryos are obscure but are gradually re-established through development. The establishment of the TAD structure requires DNA replication but not zygotic genome activation. Furthermore, unmethylated CpGs are enriched in A compartment, and methylation levels are decreased to a greater extent in A compartment than in B compartment in embryos. In summary, the global reprogramming of chromatin architecture occurs during early mammalian development.
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