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Guidance of regulatory T cell development by Satb1-dependent super-enhancer establishment.


ABSTRACT: Most Foxp3+ regulatory T (Treg) cells develop in the thymus as a functionally mature T cell subpopulation specialized for immune suppression. Their cell fate appears to be determined before Foxp3 expression; yet molecular events that prime Foxp3- Treg precursor cells are largely obscure. We found that Treg cell-specific super-enhancers (Treg-SEs), which were associated with Foxp3 and other Treg cell signature genes, began to be activated in Treg precursor cells. T cell-specific deficiency of the genome organizer Satb1 impaired Treg-SE activation and the subsequent expression of Treg signature genes, causing severe autoimmunity due to Treg cell deficiency. These results s

SUBMITTER: Kitagawa Y 

PROVIDER: S-EPMC5582804 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature

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