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Functional definition of a transcription factor hierarchy regulating T cell lineage commitment.

Authors :
Garcia-Perez L
Famili F
Cordes M
Brugman M
van Eggermond M
Wu H
Chouaref J
Granado DSL
Tiemessen MM
Pike-Overzet K
Daxinger L
Staal FJT
Source :
Science advances [Sci Adv] 2020 Jul 31; Vol. 6 (31), pp. eaaw7313. Date of Electronic Publication: 2020 Jul 31 (Print Publication: 2020).
Publication Year :
2020

Abstract

T cell factor 1 (Tcf1) is the first T cell-specific protein induced by Notch signaling in the thymus, leading to the activation of two major target genes, Gata3 and Bcl11b . Tcf1 deficiency results in partial arrests in T cell development, high apoptosis, and increased development of B and myeloid cells. Phenotypically, seemingly fully T cell-committed thymocytes with Tcf1 deficiency have promiscuous gene expression and an altered epigenetic profile and can dedifferentiate into more immature thymocytes and non-T cells. Restoring Bcl11b expression in Tcf1-deficient cells rescues T cell development but does not strongly suppress the development of non-T cells; in contrast, expressing Gata3 suppresses their development but does not rescue T cell development. Thus, T cell development is controlled by a minimal transcription factor network involving Notch signaling, Tcf1, and the subsequent division of labor between Bcl11b and Gata3, thereby ensuring a properly regulated T cell gene expression program.<br /> (Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).)

Details

Language :
English
ISSN :
2375-2548
Volume :
6
Issue :
31
Database :
MEDLINE
Journal :
Science advances
Publication Type :
Academic Journal
Accession number :
32789164
Full Text :
https://doi.org/10.1126/sciadv.aaw7313