Abstract 2215 The histone chaperone FACT maintains murine embryonic stem cell pluripotency by regulating. The genomic landscape

The FACT complex is a conserved and essential histone chaperone with roles in replication, transcription, and repair. FACT is thought to reassemble nucleosomes in vivo to promote chromatin integrity after the passage of RNA Pol II during transcription. While FACT is dispensable for most non- cancerous mammalian cell types, depletion of FACT in stem cells results in loss of pluripotency, yet, the precise mechanism through which FACT regulates cell fate decisions remains unclear. We found that AID-mediated depletion of FACT in murine embryonic stem cells (mESCs) led to increased nucleosome occupancy at loci bound by master pluripotency factors while simultaneously downregulating both mRNA and enhancer transcripts associated with Pou5f1 (OCT4), Sox2, Nanog and their targets.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2025-05-01
DOI
https://doi.org/10.1016/j.jbc.2025.109282
Primary Topic
MicroRNA in disease regulation
Type
article
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article

Abstract 2215 The histone chaperone FACT maintains murine embryonic stem cell pluripotency by regulating. The genomic landscape

Sarah J. Hainer, Rithika Sankar, Barbara Jackson, David Klein
Journal of Biological Chemistry
MicroRNA in disease regulation
article

Abstract 2215 The histone chaperone FACT maintains murine embryonic stem cell pluripotency by regulating. The genomic landscape

Sarah J. Hainer, Rithika Sankar, Barbara Jackson, David Klein
article en

Abstract

The FACT complex is a conserved and essential histone chaperone with roles in replication, transcription, and repair. FACT is thought to reassemble nucleosomes in vivo to promote chromatin integrity after the passage of RNA Pol II during transcription. While FACT is dispensable for most non- cancerous mammalian cell types, depletion of FACT in stem cells results in loss of pluripotency, yet, the precise mechanism through which FACT regulates cell fate decisions remains unclear. We found that AID-mediated depletion of FACT in murine embryonic stem cells (mESCs) led to increased nucleosome occupancy at loci bound by master pluripotency factors while simultaneously downregulating both mRNA and enhancer transcripts associated with Pou5f1 (OCT4), Sox2, Nanog and their targets.

Journal of Biological ChemistryVol. 301(5)
University of Pittsburgh (US)
Life in Land, Zero hunger
Openalex Percentile: Top 82%
MicroRNA in disease regulation
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Abstract 2215 The histone chaperone FACT maintains murine embryonic stem cell pluripotency by regulating. The genomic landscape — Sarah J. Hainer, Rithika Sankar, et al. · Journal of Biological Chemistry (2025) | TGRS Research Map | TGRS