G-quadruplex DNA structures in human stem cells and differentiation

Nat Commun. 2022 Jan 10;13(1):142. doi: 10.1038/s41467-021-27719-1.

Abstract

The establishment of cell identity during embryonic development involves the activation of specific gene expression programmes and is underpinned by epigenetic factors including DNA methylation and histone post-translational modifications. G-quadruplexes are four-stranded DNA secondary structures (G4s) that have been implicated in transcriptional regulation and cancer. Here, we show that G4s are key genomic structural features linked to cellular differentiation. We find that G4s are highly abundant in human embryonic stem cells and are lost during lineage specification. G4s are prevalent in enhancers and promoters. G4s that are found in common between embryonic and downstream lineages are tightly linked to transcriptional stabilisation of genes involved in essential cellular functions as well as transitions in the histone post-translational modification landscape. Furthermore, the application of small molecules that stabilise G4s causes a delay in stem cell differentiation, keeping cells in a more pluripotent-like state. Collectively, our data highlight G4s as important epigenetic features that are coupled to stem cell pluripotency and differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / metabolism
  • Cell Differentiation
  • Cell Line
  • Cell Lineage / genetics*
  • DNA / genetics
  • DNA / metabolism
  • DNA Methylation
  • Enhancer Elements, Genetic
  • Epigenesis, Genetic*
  • G-Quadruplexes*
  • Gene Expression
  • Histones / genetics
  • Histones / metabolism*
  • Human Embryonic Stem Cells / cytology
  • Human Embryonic Stem Cells / metabolism*
  • Humans
  • Nanog Homeobox Protein / genetics
  • Nanog Homeobox Protein / metabolism
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Nestin / genetics
  • Nestin / metabolism
  • Octamer Transcription Factor-3 / genetics
  • Octamer Transcription Factor-3 / metabolism
  • PAX6 Transcription Factor / genetics
  • PAX6 Transcription Factor / metabolism
  • Pluripotent Stem Cells / cytology
  • Pluripotent Stem Cells / metabolism*
  • Promoter Regions, Genetic
  • Protein Processing, Post-Translational*
  • Receptors, Nerve Growth Factor / genetics
  • Receptors, Nerve Growth Factor / metabolism
  • Transcription Factor AP-2 / genetics
  • Transcription Factor AP-2 / metabolism

Substances

  • Biomarkers
  • Histones
  • NANOG protein, human
  • NES protein, human
  • NGFR protein, human
  • Nanog Homeobox Protein
  • Nerve Tissue Proteins
  • Nestin
  • Octamer Transcription Factor-3
  • PAX6 Transcription Factor
  • PAX6 protein, human
  • POU5F1 protein, human
  • Receptors, Nerve Growth Factor
  • TFAP2A protein, human
  • Transcription Factor AP-2
  • DNA