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The 3D enhancer network of the developing T cell genome is shaped by SATB1.

Tomas ZelenkaAntonios KlonizakisDespina TsoukatouDionysios-Alexandros PapamatheakisSoeren FranzenburgPetros TzerposIoannis-Rafail TzonevrakisGeorge PapadogkonasManouela KapsetakiChristoforos NikolaouDariusz PlewczyńskiCharalampos G Spilianakis
Published in: Nature communications (2022)
Mechanisms of tissue-specific gene expression regulation via 3D genome organization are poorly understood. Here we uncover the regulatory chromatin network of developing T cells and identify SATB1, a tissue-specific genome organizer, enriched at the anchors of promoter-enhancer loops. We have generated a T-cell specific Satb1 conditional knockout mouse which allows us to infer the molecular mechanisms responsible for the deregulation of its immune system. H3K27ac HiChIP and Hi-C experiments indicate that SATB1-dependent promoter-enhancer loops regulate expression of master regulator genes (such as Bcl6), the T cell receptor locus and adhesion molecule genes, collectively being critical for cell lineage specification and immune system homeostasis. SATB1-dependent regulatory chromatin loops represent a more refined layer of genome organization built upon a high-order scaffold provided by CTCF and other factors. Overall, our findings unravel the function of a tissue-specific factor that controls transcription programs, via spatial chromatin arrangements complementary to the chromatin structure imposed by ubiquitously expressed genome organizers.
Keyphrases
  • transcription factor
  • genome wide
  • gene expression
  • dna methylation
  • genome wide identification
  • binding protein
  • dna damage
  • single cell
  • stem cells
  • escherichia coli
  • pseudomonas aeruginosa
  • bioinformatics analysis