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T Helper Cell Fate Specified by Kinase-Mediated Interaction of T-bet with GATA-3
Eun Sook Hwang,1Susanne J. Szabo,1*Pamela L. Schwartzberg,3Laurie H. Glimcher1,2
Cell lineage specification depends on both gene activation andgene silencing, and in the differentiation of T helper progenitorsto Th1 or Th2 effector cells, this requires the action of twoopposing transcription factors, T-bet and GATA-3. T-bet is essentialfor the development of Th1 cells, and GATA-3 performs an equivalentrole in Th2 development. We report that T-bet represses Th2lineage commitment through tyrosine kinasemediated interactionbetween the two transcription factors that interferes with thebinding of GATA-3 to its target DNA. These results provide anovel function for tyrosine phosphorylation of a transcriptionfactor in specifying alternate fates of a common progenitorcell.
1 Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA. 2 Department of Medicine, Harvard Medical School, Boston, MA 02115, USA. 3 National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
* Present address: Novartis Pharmaceuticals, Cambridge, MA 02115,USA.
To whom correspondence should be addressed. E-mail: lglimche{at}hsph.harvard.edu
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