Transcriptional repression of Gata3 is essential for early B cell commitment

Immunity. 2013 May 23;38(5):930-42. doi: 10.1016/j.immuni.2013.01.014. Epub 2013 May 16.

Abstract

The mechanisms underlying the silencing of alternative fate potentials in very early B cell precursors remain unclear. Using gain- and loss-of-function approaches together with a synthetic Zinc-finger polypeptide (6ZFP) engineered to prevent transcription factor binding to a defined cis element, we show that the transcription factor EBF1 promotes B cell lineage commitment by directly repressing expression of the T-cell-lineage-requisite Gata3 gene. Ebf1-deficient lymphoid progenitors exhibited increased T cell lineage potential and elevated Gata3 transcript expression, whereas enforced EBF1 expression inhibited T cell differentiation and caused rapid loss of Gata3 mRNA. Notably, 6ZFP-mediated perturbation of EBF1 binding to a Gata3 regulatory region restored Gata3 expression, abrogated EBF1-driven suppression of T cell differentiation, and prevented B cell differentiation via a GATA3-dependent mechanism. Furthermore, EBF1 binding to Gata3 regulatory sites induced repressive histone modifications across this region. These data identify a transcriptional circuit critical for B cell lineage commitment.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism*
  • Cell Differentiation / immunology
  • Cell Lineage / genetics
  • Cells, Cultured
  • Female
  • GATA3 Transcription Factor / genetics*
  • GATA3 Transcription Factor / metabolism*
  • Gene Expression
  • Gene Expression Regulation
  • Hepatocyte Nuclear Factor 1-alpha / metabolism
  • Histones / metabolism
  • Lymphoid Progenitor Cells / metabolism
  • Lymphopoiesis / genetics
  • Mice
  • Mice, Inbred C57BL
  • RNA, Messenger / biosynthesis
  • Receptor, Notch1 / metabolism
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism*
  • Trans-Activators / deficiency
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Transcription, Genetic
  • Zinc Fingers / genetics

Substances

  • Ebf1 protein, mouse
  • GATA3 Transcription Factor
  • Gata3 protein, mouse
  • Hepatocyte Nuclear Factor 1-alpha
  • Histones
  • Hnf1a protein, mouse
  • Notch1 protein, mouse
  • RNA, Messenger
  • Receptor, Notch1
  • Trans-Activators

Associated data

  • GEO/GSE46004