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The diverse lineages of the mammalian hematopoietic system including both B and T lymphocytes are derived from a single mesodermal progeni tor, the pluripotent bone marrow stem cell. The coordinate transcriptional regulation of sets oflineage-specific genes is one of the important molecular mechanisms underlying hematopoietic lineage determination and differ entiation. The immunoglobulin and T cell receptor (TCR) genes have been used as model systems to study lineage-specific transcriptional regulation during lymphoid development. This review summarizes our current under standing of the regulation of TCR gene expression during thymocyte ontogeny. Expression of each of the TCR genes is controlled by T cell specific transcriptional enhancers that bind partially overlapping sets of ubiquitous and lymphoid-specific transcription factors. These include members of both the A TF(CREB family of basic-leucine zipper proteins and the Ets protooncogene family, as well as the T cell-specific zinc finger transcription factor, GATA-3, and the T cell-specific high mobility group proteins TCF-l and TCF-lct/LEF-l. The identification of binding sites for these same transcription factors in a number of additional T cell specific genes suggests that they may play important roles in the coordinate regulation of gene expression that specifies the development of the T cell lineages. Recent
Annual Review of Immunology – Annual Reviews
Published: Apr 1, 1993
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