T-cell factor 1 is a gatekeeper for T-cell specification in response to Notch signaling

Although transcriptional programs associated with T-cell specification and commitment have been described, the functional hierarchy and the roles of key regulators in structuring/orchestrating these programs remain unclear. Activation of Notch signaling in uncommitted precursors by the thymic stroma...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2011-12, Vol.108 (50), p.20060-20065
Hauptverfasser: Germar, Kristine, Dose, Marei, Konstantinou, Tassos, Zhang, Jiangwen, Wang, Hongfang, Lobry, Camille, Arnett, Kelly L, Blacklow, Stephen C, Aifantis, Iannis, Aster, Jon C, Gounari, Fotini
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Sprache:eng
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Zusammenfassung:Although transcriptional programs associated with T-cell specification and commitment have been described, the functional hierarchy and the roles of key regulators in structuring/orchestrating these programs remain unclear. Activation of Notch signaling in uncommitted precursors by the thymic stroma initiates the T-cell differentiation program. One regulator first induced in these precursors is the DNA-binding protein T-cell factor 1 (Tcf-1), a T-cell–specific mediator of Wnt signaling. However, the specific contribution of Tcf-1 to early T-cell development and the signals inducing it in these cells remain unclear. Here we assign functional significance to Tcf-1 as a gatekeeper of T-cell fate and show that Tcf-1 is directly activated by Notch signals. Tcf-1 is required at the earliest phase of T-cell determination for progression beyond the early thymic progenitor stage. The global expression profile of Tcf-1–deficient progenitors indicates that basic processes of DNA metabolism are down-regulated in its absence, and the blocked T-cell progenitors become abortive and die by apoptosis. Our data thus add an important functional relationship to the roadmap of T-cell development.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.1110230108