4.5 Article

Early embryonic-like cells are induced by downregulating replication-dependent chromatin assembly

期刊

NATURE STRUCTURAL & MOLECULAR BIOLOGY
卷 22, 期 9, 页码 662-U35

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb.3066

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资金

  1. EpiGeneSys NoE
  2. ERC-Stg 'NuclearPotency'
  3. FP7 Marie-Curie Actions ITN Nucleosome4D
  4. European Molecular Biology Organization Young Investigator Programme
  5. Fondation Schlumberger pour l'Education et la Recherche
  6. Deutsche Forschungsgemeinschaft Cells-in-Motion Cluster of Excellence [EXC 1003-CiM]
  7. University of Munster
  8. Max Planck Society
  9. KAKENHI [23248048]
  10. Takeda Science Foundation
  11. Uehara Memorial Foundation
  12. Human Frontier Science Programme
  13. Association pour la Recherche Contre le Cancer
  14. Direccion General de Cooperacion e Internacionalizacion fellowship from the National University of Mexico
  15. [ANR-10-LABX-0030-INRT]
  16. Grants-in-Aid for Scientific Research [23248048] Funding Source: KAKEN

向作者/读者索取更多资源

Cellular plasticity is essential for early embryonic cells. Unlike pluripotent cells, which form embryonic tissues, totipotent cells can generate a complete organism including embryonic and extraembryonic tissues. Cells resembling 2-cell-stage embryos (2C-like cells) arise at very low frequency in embryonic stem (ES) cell cultures. Although induced reprogramming to pluripotency is well established, totipotent cells remain poorly characterized, and whether reprogramming to totipotency is possible is unknown. We show that mouse 2C-like cells can be induced in vitro through downregulation of the chromatin-assembly activity of CAF-1. Endogenous retroviruses and genes specific to 2-cell embryos are the highest-upregulated genes upon CAF-1 knockdown. Emerging 2C-like cells exhibit molecular characteristics of 2-cell embryos and higher reprogrammability than ES cells upon nuclear transfer. Our results suggest that early embryonic-like cells can be induced by modulating chromatin assembly and that atypical histone deposition may trigger the emergence of totipotent cells.

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