NANOG prion-like assembly mediates DNA bridging to facilitate chromatin reorganization and activation of pluripotency

Human NANOG expression resets stem cells to ground-state pluripotency. Here we identify the unique features of human NANOG that relate to its dose-sensitive function as a master transcription factor. NANOG is largely disordered, with a C-terminal prion-like domain that phase-transitions to gel-like...

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Veröffentlicht in:Nature cell biology 2022-05, Vol.24 (5), p.737-747
Hauptverfasser: Choi, Kyoung-Jae, Quan, My Diem, Qi, Chuangye, Lee, Joo-Hyung, Tsoi, Phoebe S., Zahabiyon, Mahla, Bajic, Aleksandar, Hu, Liya, Prasad, B. V. Venkataram, Liao, Shih-Chu Jeff, Li, Wenbo, Ferreon, Allan Chris M., Ferreon, Josephine C.
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Sprache:eng
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Zusammenfassung:Human NANOG expression resets stem cells to ground-state pluripotency. Here we identify the unique features of human NANOG that relate to its dose-sensitive function as a master transcription factor. NANOG is largely disordered, with a C-terminal prion-like domain that phase-transitions to gel-like condensates. Full-length NANOG readily forms higher-order oligomers at low nanomolar concentrations, orders of magnitude lower than typical amyloids. Using single-molecule Förster resonance energy transfer and fluorescence cross-correlation techniques, we show that NANOG oligomerization is essential for bridging DNA elements in vitro. Using chromatin immunoprecipitation sequencing and Hi-C 3.0 in cells, we validate that NANOG prion-like domain assembly is essential for specific DNA recognition and distant chromatin interactions. Our results provide a physical basis for the indispensable role of NANOG in shaping the pluripotent genome. NANOG’s unique ability to form prion-like assemblies could provide a cooperative and concerted DNA bridging mechanism that is essential for chromatin reorganization and dose-sensitive activation of ground-state pluripotency. Choi et al. report that human NANOG proteins form gel-like condensates at extremely low concentrations, which facilitate the chromatin interaction that is essential for pluripotency maintenance.
ISSN:1465-7392
1476-4679
DOI:10.1038/s41556-022-00896-x