NANOG prion-like assembly mediates DNA bridging to facilitate chromatin reorganization and activation of pluripotency.
Kyoung-Jae ChoiMy Diem QuanChuangye QiJoo-Hyung LeePhoebe S TsoiMahla ZahabiyonAleksandar BajicLiya HuB V Venkataram PrasadShih-Chu Jeff LiaoWenbo LiAllan Chris M FerreonJosephine C FerreonPublished in: Nature cell biology (2022)
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.
Keyphrases
- single molecule
- energy transfer
- cancer stem cells
- embryonic stem cells
- transcription factor
- stem cells
- circulating tumor
- dna damage
- gene expression
- genome wide
- endothelial cells
- cell free
- atomic force microscopy
- quantum dots
- induced apoptosis
- living cells
- poor prognosis
- physical activity
- lymph node
- mental health
- single cell
- mesenchymal stem cells
- cell therapy
- bone marrow
- nucleic acid