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      3D Chromatin Structures of Mature Gametes and Structural Reprogramming during Mammalian Embryogenesis.

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          Abstract

          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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          Author and article information

          Journal
          Cell
          Cell
          Elsevier BV
          1097-4172
          0092-8674
          Jul 13 2017
          : 170
          : 2
          Affiliations
          [1 ] CAS Key Laboratory of Genome Sciences and Information, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China; University of Chinese Academy of Sciences, Beijing, China.
          [2 ] School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
          [3 ] School of Life Science and Technology, ShanghaiTech University, Shanghai, China; University of Chinese Academy of Sciences, Beijing, China; Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
          [4 ] CAS Key Laboratory of Genome Sciences and Information, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.
          [5 ] Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
          [6 ] MOE Key Laboratory of Bioinformatics, Center for Stem Cell Biology and Regenerative Medicine, THU-PKU Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China.
          [7 ] School of Life Science and Technology, ShanghaiTech University, Shanghai, China. Electronic address: huangxx@shanghaitech.edu.cn.
          [8 ] CAS Key Laboratory of Genome Sciences and Information, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China; University of Chinese Academy of Sciences, Beijing, China. Electronic address: liuj@big.ac.cn.
          Article
          S0092-8674(17)30713-4
          10.1016/j.cell.2017.06.029
          28709003
          e3a3bcbb-7acc-41e1-871c-c58743bc7c1d
          History

          Hi-C,TAD,chromatin structure,compartment,embryo development,epigenetic,gamete,zygotic genome activation

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