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EMBO J. 2007 Aug 8;26(15):3629-40. Epub 2007 Jul 19.

c-Myb regulates lineage choice in developing thymocytes via its target gene Gata3.

Author information

1
Institute of Cancer Research, Cancer Research UK Centre for Cell and Molecular Biology, London, UK.

Abstract

During T-cell development, thymocytes with intermediate avidity for antigen-MHC complexes are positively selected and then differentiate into functional cytotoxic and helper T cells. This process is controlled by signalling from the T-cell receptor (TCR). Here, we show that the c-Myb transcription factor is a critical downstream regulator of positive selection, promoting the development of helper T cells and blocking the development of cytotoxic T cells. A gain-of-function c-Myb transgene stops development of cytotoxic T cells, instead causing accumulation of a precursor population. Conversely, loss of c-Myb in selecting cells results in significantly fewer helper T cells. In c-Myb-null thymocytes, Gata3, a critical inducer of T-helper cell fate, is not upregulated in response to T-cell receptor signaling, following selection. We show that Gata3 is a direct target of c-Myb, and propose that c-Myb is an important regulator of Gata3, required for transduction of the T-cell receptor signal for subsequent helper cell lineage differentiation.

PMID:
17641686
PMCID:
PMC1949015
DOI:
10.1038/sj.emboj.7601801
[Indexed for MEDLINE]
Free PMC Article

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