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

Author:

Choi Kyoung-JaeORCID,Quan My Diem,Qi Chuangye,Lee Joo-Hyung,Tsoi Phoebe S.,Zahabiyon Mahla,Bajic Aleksandar,Hu LiyaORCID,Prasad B. V. VenkataramORCID,Liao Shih-Chu Jeff,Li WenboORCID,Ferreon Allan Chris M.ORCID,Ferreon Josephine C.

Abstract

AbstractHuman 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.

Funder

U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences

Cancer Prevention and Research Institute of Texas

U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute

Welch Foundation

U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology

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