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<p>Specification of primordial germ cells (PGCs) establishes germline development during early embryogenesis, yet the underlying mechanisms in humans remain largely unknown. Here, we reveal the functional roles of germline-specific RNA-binding protein (RBP) DND1 in human PGC (hPGC) specification. We discovered that DND1 forms a complex with another RBP, NANOS3, to restrict hPGC specification. Furthermore, by analyzing the mRNAs bound by DND1 and NANOS3, we found that DND1 facilitates the binding of NANOS3 to hPGC-like cells-related mRNAs. We identified <i>SOX4</i> mRNAs as the key downstream factor for the DND1 and NANOS3 complex. Mechanistically, DND1 and NANOS3 function in processing bodies (P-bodies) to repress the translation of <i>SOX4</i> mRNAs, with NANOS3 mediating the interaction between DND1 and the translational repressor 4E-T. Altogether, these findings identify the RBP complex formed by DND1 and NANOS3 functioning as a “braking system” to restrict the entry of germ cell fate in humans.</p>

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RNA-binding proteins DND1 and NANOS3 cooperatively suppress the entry of germ cell lineage

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年5月23日

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  • Ziqi Wang,
  • Honglin Yu,
  • Zhaoyu Gu,
  • Xiaohui Shi,
  • Jiayue Ma,
  • Qizhe Shao,
  • Yao Yao,
  • Shuo Yao,
  • Yan Xu,
  • Yashi Gu,
  • Jiayue Dai,
  • Qi Liu,
  • Jingyan Shi,
  • Rujie Qi,
  • Yue Jin,
  • Yuqian Liu,
  • Xinchen Shen,
  • Wenwen Huang,
  • Heng-Jia Liu,
  • Min Jin,
  • Wanlu Liu,
  • Matthew Brook,
  • Di Chen

摘要

Specification of primordial germ cells (PGCs) establishes germline development during early embryogenesis, yet the underlying mechanisms in humans remain largely unknown. Here, we reveal the functional roles of germline-specific RNA-binding protein (RBP) DND1 in human PGC (hPGC) specification. We discovered that DND1 forms a complex with another RBP, NANOS3, to restrict hPGC specification. Furthermore, by analyzing the mRNAs bound by DND1 and NANOS3, we found that DND1 facilitates the binding of NANOS3 to hPGC-like cells-related mRNAs. We identified SOX4 mRNAs as the key downstream factor for the DND1 and NANOS3 complex. Mechanistically, DND1 and NANOS3 function in processing bodies (P-bodies) to repress the translation of SOX4 mRNAs, with NANOS3 mediating the interaction between DND1 and the translational repressor 4E-T. Altogether, these findings identify the RBP complex formed by DND1 and NANOS3 functioning as a “braking system” to restrict the entry of germ cell fate in humans.