Rangatia Janki, Vangala Rajani Kanth, Treiber Nicolai, Zhang Pu, Radomska Hanna, Tenen Daniel G, Hiddemann Wolfgang, Behre Gerhard
Department of Medicine III, Ludwig Maximilians University Munich, and GSF-National Research Center, Munich, Germany.
Mol Cell Biol. 2002 Dec;22(24):8681-94. doi: 10.1128/MCB.22.24.8681-8694.2002.
The transcription factor C/EBPalpha is crucial for the differentiation of granulocytes. Conditional expression of C/EBPalpha triggers neutrophilic differentiation, and C/EBPalpha can block 12-O-tetradecanoylphorbol-13-acetate-induced monocytic differentiation of bipotential myeloid cells. In C/EBPalpha knockout mice, no mature granulocytes are present. A dramatic increase of c-Jun mRNA in C/EBPalpha knockout mouse fetal liver was observed. c-Jun, a component of the AP-1 transcription factor complex and a coactivator of the transcription factor PU.1, is important for monocytic differentiation. Here we report that C/EBPalpha downregulates c-Jun expression to drive granulocytic differentiation. An ectopic increase of C/EBPalpha expression decreases the c-Jun mRNA level, and the human c-Jun promoter activity is downregulated eightfold in the presence of C/EBPalpha. C/EBPalpha and c-Jun interact through their leucine zipper domains, and this interaction prevents c-Jun from binding to DNA. This results in downregulation of c-Jun's capacity to autoregulate its own promoter through the proximal AP-1 site. Overexpression of c-Jun prevents C/EBPalpha-induced granulocytic differentiation. Thus, we propose a model in which C/EBPalpha needs to downregulate c-Jun expression and transactivation capacity for promoting granulocytic differentiation.
转录因子C/EBPα对粒细胞的分化至关重要。C/EBPα的条件性表达可触发嗜中性粒细胞分化,且C/EBPα能阻断12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯诱导的双能髓系细胞的单核细胞分化。在C/EBPα基因敲除小鼠中,不存在成熟的粒细胞。在C/EBPα基因敲除小鼠的胎肝中观察到c - Jun mRNA显著增加。c - Jun是AP - 1转录因子复合物的一个组分以及转录因子PU.1的共激活因子,对单核细胞分化很重要。在此我们报道,C/EBPα下调c - Jun表达以驱动粒细胞分化。C/EBPα表达的异位增加会降低c - Jun mRNA水平,并且在有C/EBPα存在的情况下,人c - Jun启动子活性下调8倍。C/EBPα和c - Jun通过它们的亮氨酸拉链结构域相互作用,这种相互作用阻止c - Jun与DNA结合。这导致c - Jun通过近端AP - 1位点自动调节其自身启动子的能力下调。c - Jun的过表达会阻止C/EBPα诱导的粒细胞分化。因此,我们提出一个模型,其中C/EBPα需要下调c - Jun表达和反式激活能力以促进粒细胞分化。