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Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation

Author

Listed:
  • Xiaoqing Nie

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

  • Qianhua Xu

    (Tsinghua University
    Tsinghua-Peking Center for Life Sciences)

  • Chengpeng Xu

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

  • Fengling Chen

    (Tsinghua University
    Tsinghua-Peking Center for Life Sciences)

  • Qizhi Wang

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

  • Dandan Qin

    (Chinese Academy of Sciences)

  • Rui Wang

    (Chinese Academy of Sciences)

  • Zheng Gao

    (Reproductive Medicine Center of the Third Affiliated Hospital of Guangzhou Medical University)

  • Xukun Lu

    (Tsinghua University
    Tsinghua-Peking Center for Life Sciences)

  • Xinai Yang

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

  • Yu Wu

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

  • Chen Gu

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

  • Wei Xie

    (Tsinghua University
    Tsinghua-Peking Center for Life Sciences)

  • Lei Li

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

Abstract

Zygotic genome activation (ZGA) is essential for early embryonic development. However, the regulation of ZGA remains elusive in mammals. Here we report that a maternal factor TDP-43, a nuclear transactive response DNA-binding protein, regulates ZGA through RNA Pol II and is essential for mouse early embryogenesis. Maternal TDP-43 translocates from the cytoplasm into the nucleus at the early two-cell stage when minor to major ZGA transition occurs. Genetic deletion of maternal TDP-43 results in mouse early embryos arrested at the two-cell stage. TDP-43 co-occupies with RNA Pol II as large foci in the nucleus and also at the promoters of ZGA genes at the late two-cell stage. Biochemical evidence indicates that TDP-43 binds Polr2a and Cyclin T1. Depletion of maternal TDP-43 caused the loss of Pol II foci and reduced Pol II binding on chromatin at major ZGA genes, accompanied by defective ZGA. Collectively, our results suggest that maternal TDP-43 is critical for mouse early embryonic development, in part through facilitating the correct RNA Pol II configuration and zygotic genome activation.

Suggested Citation

  • Xiaoqing Nie & Qianhua Xu & Chengpeng Xu & Fengling Chen & Qizhi Wang & Dandan Qin & Rui Wang & Zheng Gao & Xukun Lu & Xinai Yang & Yu Wu & Chen Gu & Wei Xie & Lei Li, 2023. "Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-39924-1
    DOI: 10.1038/s41467-023-39924-1
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