4.7 Article

Transcription factor Foxp3 and its protein partners form a complex regulatory network

Journal

NATURE IMMUNOLOGY
Volume 13, Issue 10, Pages 1010-1019

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ni.2402

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Funding

  1. US National Institutes of Health [R37 AI034206]
  2. Howard Hughes Medical Institute
  3. Arthritis Foundation postdoctoral fellowship
  4. Cancer Research Institute
  5. National Institutes of Health Medical Scientist Training Program grant [GM07739]
  6. National Institute of Neurological Disorders and Stroke [1F31NS073203-01]
  7. National Institutes of Health [DK091968]
  8. Medical Scientist Training Program [GM07739]

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The transcription factor Foxp3 is indispensible for the differentiation and function of regulatory T cells (T-reg cells). To gain insights into the molecular mechanisms of Foxp3-mediated gene expression, we purified Foxp3 complexes and explored their composition. Biochemical and mass-spectrometric analyses revealed that Foxp3 forms multiprotein complexes of 400-800 kDa or larger and identified 361 associated proteins, similar to 30% of which were transcription related. Foxp3 directly regulated expression of a large proportion of the genes encoding its cofactors. Some transcription factor partners of Foxp3 facilitated its expression. Functional analysis of the cooperation of Foxp3 with one such partner, GATA-3, provided additional evidence for a network of transcriptional regulation afforded by Foxp3 and its associates to control distinct aspects of T-reg cell biology.

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