E2A transcription factors limit expression of Gata3 to facilitate T lymphocyte lineage commitment

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E2A transcription factors limit expression of Gata3 to facilitate T lymphocyte lineage commitment.

The E2A transcription factors promote the development of thymus-seeding cells, but it remains unknown whether these proteins play a role in T lymphocyte lineage specification or commitment. Here, we showed that E2A proteins were required to promote T-lymphocyte commitment from DN2 thymocytes and to extinguish their potential for alternative fates. E2A proteins functioned in DN2 cells to limit e...

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Transcription factor expression dynamics of early T-lymphocyte specification and commitment.

Mammalian T lymphocytes are a prototype for development from adult pluripotent stem cells. While T-cell specification is driven by Notch signaling, T-lineage commitment is only finalized after prolonged Notch activation. However, no T-lineage specific regulatory factor has been reported that mediates commitment. We used a gene-discovery approach to identify additional candidate T-lineage transc...

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Growth factor independent 1B (Gfi1b) is an E2A target gene that modulates Gata3 in T-cell lymphomas.

The E2A transcription factors are required for normal T lymphopoiesis and to prevent T-lymphocyte progenitor transformation. Ectopic expression of E2A proteins in E2A-deficient lymphomas results in growth arrest and apoptosis, indicating that these cells remain responsive to the targets of E2A. Here we identify the transcriptional repressor growth factor independent 1B (Gfi1b) as a target of E2...

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The E2A transcription factors are required for normal T lymphopoiesis and to prevent T lymphocyte progenitor transformation. Ectopic expression of E2A proteins in E2Adeficient lymphomas results in growth arrest and apoptosis indicating that these cells remain responsive to the targets of E2A. Here we identify the transcriptional repressor Growth factor independence (Gfi) 1b as a target of E2A t...

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ژورنال

عنوان ژورنال: Blood

سال: 2013

ISSN: 0006-4971,1528-0020

DOI: 10.1182/blood-2012-08-449447