Travis A, Amsterdam A, Belanger C, Grosschedl R
Howard Hughes Medical Institute, University of California, San Francisco 94143-0414.
Genes Dev. 1991 May;5(5):880-94. doi: 10.1101/gad.5.5.880.
Lymphoid-specific cDNA clones were isolated that encode a nuclear protein with homology to the chromosomal nonhistone protein HMG-1 and to putative regulators of cell specialization, including the mammalian testis-determining factor SRY and fungal mating-type proteins. The gene represented by the isolated cDNA clones, termed LEF-1 (lymphoid enhancer-binding factor 1), is developmentally regulated and expressed in pre-B and T lymphocytes but not in later-stage B cells or nonlymphoid tissues. Both endogenous and recombinant LEF-1 were shown to bind to a functionally important site in the T-cell antigen receptor (TCR) alpha enhancer. Maximal TCR alpha enhancer activity was found to parallel the cell type-specific expression pattern of LEF-1. Moreover, forced expression of recombinant LEF-1 in late stage B cells increases TCR alpha enhancer function. Taken together, these data suggest that LEF-1 is a regulatory participant in lymphocyte gene expression and differentiation.
分离出了淋巴细胞特异性cDNA克隆,其编码一种核蛋白,该核蛋白与染色体非组蛋白HMG-1以及细胞特化的假定调节因子具有同源性,这些调节因子包括哺乳动物的睾丸决定因子SRY和真菌交配型蛋白。由分离出的cDNA克隆所代表的基因,称为LEF-1(淋巴细胞增强子结合因子1),其表达受发育调控,在B前淋巴细胞和T淋巴细胞中表达,但在后期B细胞或非淋巴细胞组织中不表达。内源性和重组LEF-1均显示与T细胞抗原受体(TCR)α增强子中的一个功能重要位点结合。发现最大的TCRα增强子活性与LEF-1的细胞类型特异性表达模式平行。此外,在后期B细胞中强制表达重组LEF-1可增强TCRα增强子功能。综上所述,这些数据表明LEF-1是淋巴细胞基因表达和分化的调节参与者。