Molecular Medicine Branch, NIDDK, National Institutes of Health, Bethesda, Maryland 20892-1822, USA.
J Biol Chem. 2012 Oct 26;287(44):36720-31. doi: 10.1074/jbc.M112.378398. Epub 2012 Sep 16.
During erythropoiesis, erythropoietin stimulates induction of erythroid transcription factors that activate expression of erythroid genes including the erythropoietin receptor (EPO-R) that results in increased sensitivity to erythropoietin. DNA binding of the basic helix-loop-helix transcription factor, TAL1/SCL, is required for normal erythropoiesis. A link between elevated TAL1 and excessive erythrocytosis is suggested by erythroid progenitor cells from a patient that exhibits unusually high sensitivity to erythropoietin with concomitantly elevated TAL1 and EPO-R expression. We found that TAL1 regulates EPO-R expression mediated via three conserved E-box binding motifs (CAGCTG) in the EPO-R 5' untranslated transcribed region. TAL1 increases association of the GATA-1·TAL1·LMO2·LDB1 transcription activation complex to the region that includes the transcription start site and the 5' GATA and 3' E-box motifs flanking the EPO-R transcription start site suggesting that TAL1 promotes accessibility of this region. Nucleosome shifting has been demonstrated to facilitate TAL1 but not GATA-1 binding to regulate target gene expression. Accordingly, we observed that with induced expression of EPO-R in hemotopoietic progenitor cells, nucleosome phasing shifts to increase the linker region containing the EPO-R transcription start site and TAL1 binds to the flanking 5' GATA and 3' E-box regions of the promoter. These data suggest that TAL1 binds to the EPO-R promoter to activate EPO-R expression and provides a potential link to elevated EPO-R expression leading to hypersensitivity to erythropoietin and the resultant excessive erythrocytosis.
在红细胞生成过程中,促红细胞生成素刺激红细胞转录因子的诱导,激活包括促红细胞生成素受体(EPO-R)在内的红细胞基因的表达,从而增加对促红细胞生成素的敏感性。碱性螺旋-环-螺旋转录因子 TAL1/SCL 的 DNA 结合对于正常的红细胞生成是必需的。一名患者的红细胞祖细胞表现出对促红细胞生成素异常高的敏感性,同时伴有 TAL1 和 EPO-R 表达的升高,这表明 TAL1 与过多的红细胞增多之间存在联系。我们发现 TAL1 通过三个保守的 E 盒结合基序(CAGCTG)调节 EPO-R 表达,该基序位于 EPO-R 5'非翻译转录区。TAL1 增加了 GATA-1·TAL1·LMO2·LDB1 转录激活复合物与包括转录起始位点和 5' GATA 和 3' E 盒侧翼 EPO-R 转录起始位点的区域的结合,这表明 TAL1 促进了该区域的可及性。已经证明核小体转移有助于 TAL1 但不 GATA-1 结合以调节靶基因表达。因此,我们观察到在造血祖细胞中 EPO-R 的诱导表达,核小体相位转移增加了包含 EPO-R 转录起始位点的连接区,并且 TAL1 结合到启动子侧翼的 5' GATA 和 3' E 盒区域。这些数据表明,TAL1 结合到 EPO-R 启动子上以激活 EPO-R 表达,并提供了一个潜在的联系,以提高 EPO-R 表达导致对促红细胞生成素的过度敏感和由此产生的红细胞增多症。