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BMP4 drives primed to naïve transition through PGC-like state

Author

Listed:
  • Shengyong Yu

    (Chinese Academy of Sciences)

  • Chunhua Zhou

    (Chinese Academy of Sciences)

  • Jiangping He

    (Bioland Laboratory)

  • Zhaokai Yao

    (Southern Medical University)

  • Xingnan Huang

    (Westlake University)

  • Bowen Rong

    (Fudan University)

  • Hong Zhu

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Shijie Wang

    (Guangzhou Medical University)

  • Shuyan Chen

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Xialian Wang

    (Guangzhou Medical University)

  • Baomei Cai

    (Bioland Laboratory)

  • Guoqing Zhao

    (Bioland Laboratory)

  • Yuhan Chen

    (Southern Medical University)

  • Lizhan Xiao

    (Bioland Laboratory)

  • He Liu

    (Bioland Laboratory)

  • Yue Qin

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Jing Guo

    (Chinese Academy of Sciences)

  • Haokaifeng Wu

    (Chinese Academy of Sciences)

  • Zhen Zhang

    (Chinese Academy of Sciences)

  • Man Zhang

    (Bioland Laboratory)

  • Xiaoyang Zhao

    (Southern Medical University)

  • Fei Lan

    (Fudan University)

  • Yixuan Wang

    (Chinese Academy of Sciences
    University of Science and Technology of China)

  • Jiekai Chen

    (Chinese Academy of Sciences
    Bioland Laboratory)

  • Shangtao Cao

    (Bioland Laboratory)

  • Duanqing Pei

    (Westlake University)

  • Jing Liu

    (Chinese Academy of Sciences
    Bioland Laboratory)

Abstract

Multiple pluripotent states have been described in mouse and human stem cells. Here, we apply single-cell RNA-seq to a newly established BMP4 induced mouse primed to naïve transition (BiPNT) system and show that the reset is not a direct reversal of cell fate but goes through a primordial germ cell-like cells (PGCLCs) state. We first show that epiblast stem cells bifurcate into c-Kit+ naïve and c-Kit− trophoblast-like cells, among which, the naïve branch undergoes further transition through a PGCLCs intermediate capable of spermatogenesis in vivo. Mechanistically, we show that DOT1L inhibition permits the transition from primed pluripotency to PGCLCs in part by facilitating the loss of H3K79me2 from Gata3/6. In addition, Prdm1/Blimp1 is required for PGCLCs and naïve cells, while Gata2 inhibits PGC-like state by promoting trophoblast-like fate. Our work not only reveals an alternative route for primed to naïve transition, but also gains insight into germ cell development.

Suggested Citation

  • Shengyong Yu & Chunhua Zhou & Jiangping He & Zhaokai Yao & Xingnan Huang & Bowen Rong & Hong Zhu & Shijie Wang & Shuyan Chen & Xialian Wang & Baomei Cai & Guoqing Zhao & Yuhan Chen & Lizhan Xiao & He , 2022. "BMP4 drives primed to naïve transition through PGC-like state," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30325-4
    DOI: 10.1038/s41467-022-30325-4
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