McNagny K M, Sieweke M H, Döderlein G, Graf T, Nerlov C
Department of Medical Genetics, Biomedical Research Centre, University of British Columbia, Vancouver, BC, Canada V6T 1Z3.
EMBO J. 1998 Jul 1;17(13):3669-80. doi: 10.1093/emboj/17.13.3669.
The EOS47 antigen is an early and specific marker of eosinophil differentiation in the chicken haematopoietic system. To elucidate the transciptional events controlling commitment to the eosinophil lineage, we studied the regulation of the eosinophil-specific EOS47 promoter. This promoter is TATA-less, and binds trancription factors of the Ets, C/EBP, GATA and Myb families. These sites are contained within a 309 bp promoter fragment which is sufficient for specific high level transcription in an eosinophil cell line. Co-transfection experiments in Q2bn fibroblasts showed cooperative activation of the EOS47 proximal promoter by c-Myb, Ets-1/Fli-1, GATA-1 and C/EBPalpha. The Ets-1/Fli-1 and C/EBPalpha proteins were the most potent activators, and acted with high synergy through juxtaposed binding sites located approximately 60 bp upstream of the transcription start site. The Ets-1 and C/EBPalpha proteins were found to associate physically via their DNA-binding domains and to bind their combined binding site cooperatively. GATA-1 showed biphasic regulation of the EOS47 promoter, activating at low and repressing at high protein concentrations. These results demonstrate combinatorial activation of an eosinophil-specific promoter by ubiquitous and lineage-restricted haematopoietic transcription factors. They also indicate that direct interactions between C/EBPs and specific Ets family members, together with GATA-1, are important for eosinophil lineage determination.
EOS47抗原是鸡造血系统中嗜酸性粒细胞分化的早期特异性标志物。为了阐明控制嗜酸性粒细胞谱系定向分化的转录事件,我们研究了嗜酸性粒细胞特异性EOS47启动子的调控机制。该启动子无TATA盒,可结合Ets、C/EBP、GATA和Myb家族的转录因子。这些位点存在于一个309 bp的启动子片段中,该片段足以在嗜酸性粒细胞系中进行特异性的高水平转录。在Q2bn成纤维细胞中的共转染实验表明,c-Myb、Ets-1/Fli-1、GATA-1和C/EBPα可协同激活EOS47近端启动子。Ets-1/Fli-1和C/EBPα蛋白是最有效的激活因子,它们通过位于转录起始位点上游约60 bp处的并列结合位点以高度协同的方式发挥作用。研究发现,Ets-1和C/EBPα蛋白通过其DNA结合结构域发生物理相互作用,并协同结合它们的联合结合位点。GATA-1对EOS47启动子表现出双相调控作用,在低蛋白浓度时激活,在高蛋白浓度时抑制。这些结果表明,普遍存在的和谱系限制性的造血转录因子可对嗜酸性粒细胞特异性启动子进行组合激活。它们还表明,C/EBPs与特定Ets家族成员以及GATA-1之间的直接相互作用对于嗜酸性粒细胞谱系的确定很重要。