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Esrrb is a cell-cycle-dependent associated factor balancing pluripotency and XEN differentiation.


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.

SUBMITTER: Herchcovici Levy S 

PROVIDER: S-EPMC9214067 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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Esrrb is a cell-cycle-dependent associated factor balancing pluripotency and XEN differentiation.

Herchcovici Levy Sapir S   Feldman Cohen Sharon S   Arnon Lee L   Lahav Shlomtzion S   Awawdy Muhammad M   Alajem Adi A   Bavli Danny D   Sun Xue X   Buganim Yosef Y   Ram Oren O  

Stem cell reports 20220519 6


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 cou  ...[more]

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