Mink S, Jaswal S, Burk O, Klempnauer K H
Institut für Biochemie, Universität Münster, Wilhelm-Klemm-Str. 2, D-48149, Münster, Germany.
Biochim Biophys Acta. 1999 Oct 28;1447(2-3):175-84. doi: 10.1016/s0167-4781(99)00168-2.
Previous studies have implicated the CCAAT box/enhancer binding protein beta (C/EBPbeta) in the regulation of cell-type specific gene expression in myelomonocytic cells and in the activation of target genes by the transcription factor v-Myb. To better understand the role of C/EBPbeta in myelomonocytic cells we have cloned the chicken C/EBPbeta gene and studied its regulation. The chicken C/EBPbeta promoter contains a number of C/EBP binding sites and is activated by C/EBPbeta, suggesting that the C/EBPbeta gene is autoregulated by its own protein product. Interestingly, the C/EBPbeta promoter is not activated by C/EBPalpha, another C/EBP family member highly expressed in myelomonocytic cells, indicating that the autoregulation is specific for C/EBPbeta. Comparison of different C/EBP inducible promoters shows that the relative transactivation potential of C/EBPalpha and beta is extremely dependent on the promoter context. By using the promoters of the mim-1 and C/EBPbeta genes and by exchanging the DNA-binding domains between C/EBPalpha and beta we show that the observed promoter preferences of C/EBPalpha and beta are not due to differential DNA-binding but instead depend on the transactivation domains of these proteins. The C/EBPbeta promoter also contains several Myb binding motifs, suggesting that the C/EBPbeta gene is also myb-inducible. We show that the C/EBPbeta promoter is activated synergistically by v-Myb and C/EBPbeta and that transcription of the endogenous C/EBPbeta gene is increased by v-Myb. Thus, our results identify the C/EBPbeta gene as a novel v-Myb target gene. Taken together, our data suggest a model for the regulation of C/EBPbeta expression in which v-Myb stimulates the synthesis of C/EBPbeta by enhancing an autoregulatory loop acting on the C/EBPbeta promoter.
先前的研究表明,CCAAT盒/增强子结合蛋白β(C/EBPβ)参与调节骨髓单核细胞中细胞类型特异性基因的表达,以及转录因子v-Myb对靶基因的激活。为了更好地理解C/EBPβ在骨髓单核细胞中的作用,我们克隆了鸡C/EBPβ基因并研究了其调控机制。鸡C/EBPβ启动子包含多个C/EBP结合位点,并被C/EBPβ激活,这表明C/EBPβ基因受其自身蛋白质产物的自动调节。有趣的是,C/EBPβ启动子不会被C/EBPα激活,C/EBPα是在骨髓单核细胞中高表达的另一个C/EBP家族成员,这表明这种自动调节对C/EBPβ具有特异性。对不同C/EBP诱导型启动子的比较表明,C/EBPα和β的相对反式激活潜力极大地依赖于启动子背景。通过使用mim-1和C/EBPβ基因的启动子,并在C/EBPα和β之间交换DNA结合结构域,我们发现观察到的C/EBPα和β对启动子的偏好并非由于DNA结合的差异,而是取决于这些蛋白质的反式激活结构域。C/EBPβ启动子还包含几个Myb结合基序,这表明C/EBPβ基因也可被Myb诱导。我们发现C/EBPβ启动子被v-Myb和C/EBPβ协同激活,并且内源性C/EBPβ基因的转录因v-Myb而增加。因此,我们的结果确定C/EBPβ基因为一个新的v-Myb靶基因。综上所述,我们的数据提出了一个C/EBPβ表达调控模型,其中v-Myb通过增强作用于C/EBPβ启动子的自动调节环来刺激C/EBPβ的合成。