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Runx-CBFbeta complexes control expression of the transcription factor Foxp3 in regulatory T cells.
Rudra, Dipayan; Egawa, Takeshi; Chong, Mark M W; Treuting, Piper; Littman, Dan R; Rudensky, Alexander Y.
Affiliation
  • Rudra D; Howard Hughes Medical Institute, University of Washington, Seattle, Washington, USA.
Nat Immunol ; 10(11): 1170-7, 2009 Nov.
Article in En | MEDLINE | ID: mdl-19767756
ABSTRACT
The transcription factor Foxp3 has an indispensable role in establishing stable transcriptional and functional programs of regulatory T cells (T(reg) cells). Loss of Foxp3 expression in mature T(reg) cells results in a failure of suppressor function, yet the molecular mechanisms that ensure steady, heritable Foxp3 expression in the T(reg) cell lineage remain unknown. Using T(reg) cell-specific gene targeting, we found that complexes of the transcription factors Runx and CBFbeta were required for maintenance of Foxp3 mRNA and protein expression in T(reg) cells. Consequently, mice lacking CBFbetab exclusively in the T(reg) cell lineage had a moderate lymphoproliferative syndrome. Thus, Runx-CBFbeta complexes maintain stable high expression of Foxp3 and serve as an essential determinant of T(reg) cell lineage stability.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gene Expression Regulation / T-Lymphocytes, Regulatory / Forkhead Transcription Factors / Core Binding Factor beta Subunit Limits: Animals Language: En Journal: Nat Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2009 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gene Expression Regulation / T-Lymphocytes, Regulatory / Forkhead Transcription Factors / Core Binding Factor beta Subunit Limits: Animals Language: En Journal: Nat Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2009 Type: Article Affiliation country: United States