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An early T cell lineage commitment checkpoint dependent on the transcription factor Bcl11b.

ABSTRACT: The identities of the regulators that mediate commitment of hematopoietic precursors to the T lymphocyte lineage have been unknown. The last stage of T lineage commitment in vivo involves mechanisms to suppress natural killer cell potential, to suppress myeloid and dendritic cell potential, and to silence the stem cell or progenitor cell regulatory functions that initially provide T cell receptor-independent self-renewal capability. The zinc finger transcription factor Bcl11b is T cell-specific in expression among hematopoietic cell types and is first expressed in precursors immediately before T lineage commitment. We found that Bcl11b is necessary for T lineage commitment in mice and is specifically required both to repress natural killer cell-associated genes and to down-regulate a battery of stem cell or progenitor cell genes at the pivotal stage of commitment.

SUBMITTER: Li L

PROVIDER: S-EPMC2935300 | biostudies-literature | 2010 Jul

REPOSITORIES: biostudies-literature

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An early T cell lineage commitment checkpoint dependent on the transcription factor Bcl11b.

Li Long L Leid Mark M Rothenberg Ellen V EV

Science (New York, N.Y.) 20100701 5987

The identities of the regulators that mediate commitment of hematopoietic precursors to the T lymphocyte lineage have been unknown. The last stage of T lineage commitment in vivo involves mechanisms to suppress natural killer cell potential, to suppress myeloid and dendritic cell potential, and to silence the stem cell or progenitor cell regulatory functions that initially provide T cell receptor-independent self-renewal capability. The zinc finger transcription factor Bcl11b is T cell-specific ...[more]

PMID: 20595614

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