T-bet employs diverse regulatory mechanisms to repress transcription.

Kenneth J Oestreich, Amy S Weinmann
Author Information
  1. Kenneth J Oestreich: Department of Immunology, University of Washington, Seattle, WA 98195, USA.

Abstract

Lineage-defining transcription factors are responsible for activating the signature genes required for a given cell fate. They are also needed to repress the genetic programs associated with alternative lineage decisions. The T-box transcription factor T-bet is required for CD4(+) T helper 1 (Th1) cell differentiation. Numerous studies have explored the mechanisms by which T-bet activates the Th1 gene profile, but until recently not much was known about the mechanisms that T-bet utilizes to negatively regulate alternative T helper cell differentiation pathways such as the Th2 and Th17 fates. Here, we discuss new advances in the field that highlight the diverse mechanisms that T-bet employs to antagonize the gene programs for alternative T helper cell fates.

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Grants

  1. AI07272/NIAID NIH HHS
  2. R01 AI071272/NIAID NIH HHS
  3. T32 AI007272/NIAID NIH HHS
  4. R01 AI061061/NIAID NIH HHS
  5. R56 AI061061/NIAID NIH HHS
  6. AI061061/NIAID NIH HHS

MeSH Term

Animals
CD8-Positive T-Lymphocytes
Cell Differentiation
Cell Lineage
Humans
Receptors, Antigen, T-Cell
T-Box Domain Proteins
T-Lymphocytes, Helper-Inducer

Chemicals

Receptors, Antigen, T-Cell
T-Box Domain Proteins