T-lineage specification and commitment: a gene regulation perspective.

Ellen V Rothenberg

doi:10.1016/s1044532302000787

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T-lineage specification and commitment: a gene regulation perspective.

Ellen V Rothenberg

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Abstract

T lymphocytes originate from pluripotent precursors and undergo lasting commitment to the T cell developmental fate during their processing in the thymus. Commitment includes both the acquisition of essential T cell characteristics and the foreclosing of other developmental options. Gain of T cell characteristics is probably mediated by separate mechanisms, at least in detail, from loss of alternative developmental potentials. Programmed shifts in survival requirements make changes irreversible. Here we review the current evidence identifying the regulatory components of this commitment pathway, and the first hints of how they work together. Roles for PU.1, GATA-3, and their target genes are highlighted.

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Animals Cell Lineage Gene Expression Regulation, Developmental Humans Lymphopoiesis Membrane Proteins Receptors, Notch Stem Cells T-Lymphocytes Transcription Factors Transcription, Genetic Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.Research Support, U.S. Gov't, P.H.S.Review

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Ellen V Rothenberg. 2002. T-lineage specification and commitment: a gene regulation perspective.. https://doi.org/10.1016/s1044532302000787

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