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3D Chromatin Structures of Mature Gametes and Structural Reprogramming during Mammalian Embryogenesis
Author(s) -
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
Publication year - 2017
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2017.06.029
Subject(s) - biology , chromatin , zygote , reprogramming , embryo , microbiology and biotechnology , maternal to zygotic transition , genetics , compartment (ship) , genome , dna methylation , replication timing , embryogenesis , dna , gene , gene expression , oceanography , geology
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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