Discovery of NANOG enhancers and their essential roles in self-renewal and differentiation in human embryonic stem cells
Human embryonic stem cells (hESCs) are notable for their ability to self-renew and to differentiate into all tissue types in the body. NANOG is a core regulator of hESC identity, and dynamic control of its expression is crucial to maintain the balance between self-renewal and differentiation. Transcriptional regulation depends on enhancers, but NANOG enhancers in hESCs are not well characterized. Here, we report two NANOG enhancers discovered from a CRISPR interference screen in hESCs. Deletion of a single copy of either enhancer significantly reduced NANOG expression, compromising self-renewal and increasing differentiation propensity. Interestingly, these two NANOG enhancers are involved in a tandem duplication event found in certain primates including humans but not in mice. However, the duplicated counterparts do not regulate NANOG expression. This work expands our knowledge of functional enhancers in hESCs and highlights the sensitivity of the hESC state to the dosage of core regulators and their enhancers.
Authors
- Jielin Yan (ORCID: https://orcid.org/0000-0001-9305-3942)
- Wilfred Hing Sang Wong (ORCID: https://orcid.org/0000-0001-8396-2368)
- Renhe Luo (ORCID: https://orcid.org/0009-0008-1470-4726)
- Danwei Huangfu (ORCID: https://orcid.org/0000-0002-1145-6199)
- Christina S. Leslie (ORCID: https://orcid.org/0000-0002-4571-5910)
- Dingyu Liu (ORCID: https://orcid.org/0009-0006-5870-6374)
- Bess P. Rosen (ORCID: https://orcid.org/0000-0003-1167-656X)
Institutions
- Memorial Sloan Kettering Cancer Center (US)
- Cornell University (US)
- Kettering University (US)
- Tri-Institutional PhD Program in Chemical Biology (US)
Publication Details
- Journal
- Stem Cell Reports
- Published
- 2025-05-29
- DOI
- https://doi.org/10.1016/j.stemcr.2025.102511
- Citations
- 2
- Primary Topic
- Pluripotent Stem Cells Research
- Type
- article
- Field-Weighted Citation Impact
- 1.61
Funders
- Starr Foundation
- Cycle for Survival
- National Institutes of Health
- Marie-Josée and Henry R. Kravis Center for Molecular Oncology
- National Human Genome Research Institute
- National Cancer Institute
- National Institute of General Medical Sciences
- National Institute of Diabetes and Digestive and Kidney Diseases