Abstract
Cell cycle and differentiation decisions are linked; however, the underlying principles that drive these decisions are unclear. Here, we combined cell-cycle reporter system and single-cell RNA sequencing (scRNA-seq) profiling to study the transcriptomes of embryonic stem cells (ESCs) in the context of cell-cycle states and differentiation. By applying retinoic acid, to G1 and G2/M ESCs, we show that, while both populations can differentiate toward epiblast stem cells (EpiSCs), only G2/M ESCs could differentiate into extraembryonic endoderm cells. We identified Esrrb, a pluripotency factor that is upregulated during G2/M, as a driver of extraembryonic endoderm stem cell (XEN) differentiation. Furthermore, enhancer chromatin states based on wild-type (WT) and ESRRB knockout (KO) ESCs show association of ESRRB with XEN poised enhancers. G1 cells overexpressing Esrrb allow ESCs to produce XENs, while ESRRB-KO ESCs lost their potential to differentiate into XEN. Overall, this study reveals a vital link between Esrrb and cell-cycle states during the exit from pluripotency.
Original language | English |
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Pages (from-to) | 1334-1350 |
Number of pages | 17 |
Journal | Stem Cell Reports |
Volume | 17 |
Issue number | 6 |
DOIs | |
State | Published - 14 Jun 2022 |
Keywords
- ChIP-seq and single-cell RNA-seq (scRNA-seq)
- Esrrb transcription factor
- Exit from pluripotency
- cell cycle
- cellular differentiation and lineage specification
- embryonic stem cells
- epiblast stem cells (EpiSC)
- extraembryonic endoderm stem cells(XEN)
All Science Journal Classification (ASJC) codes
- Genetics
- Biochemistry
- Cell Biology
- Developmental Biology