Rychlik Jennifer L, Hsieh Marlene, Eiden Lee E, Lewis Elaine J
Department of Biochemistry and Molecular Biology, Oregon Health and Sciences University, Portland, OR, USA.
J Mol Neurosci. 2005;27(3):281-92. doi: 10.1385/JMN:27:3:281.
The noradrenergic cell type is characterized by the expression of proteins involved in the biosynthesis, transport, and secretion of noradrenaline and is dependent on the sequential and combinatorial expression of numerous transcription factors, including Phox2a, Phox2b, dHAND, GATA2, GATA3, and MASH1. Phox2a and Phox2b transactivate the promoter of the gene encoding the noradrenergic biosynthetic enzyme, dopamine beta-hydroxylase (DBH), and dHAND potentiates the activity of Phox2a. In this study, we use chromatin immunoprecipitation assays to identify target genes of the Phox2 proteins and dHAND. All three proteins are bound to the DBH and PHOX2B promoter regions in SH-SY5Y neuroblastoma cells. The interaction between Phox2a and dHAND is analyzed by fluorescent anisotropy, which demonstrates that dHAND causes an eightfold increase in the affinity of Phox2a for its recognition sites on the DBH promoter region. The Phox2 proteins are not found on the genes encoding other noradrenergic enzymatic or transport proteins but are reciprocally bound to each other's promoters in SH-SY5Y cells. Together with Phox2a and Phox2b, dHAND is bound to the PHOX2B promoter and is also associated with the GATA2 and eHAND genes in the absence of the Phox2 proteins. These results demonstrate the direct interactions of the Phox2 and dHAND transcription factors within a noradrenergic cell type. The Phox2 proteins were found to share all target genes, whereas dHAND binds to genes independently of Phox2a.
去甲肾上腺素能细胞类型的特征在于参与去甲肾上腺素生物合成、转运和分泌的蛋白质的表达,并且依赖于多种转录因子的顺序和组合表达,包括Phox2a、Phox2b、dHAND、GATA2、GATA3和MASH1。Phox2a和Phox2b可反式激活编码去甲肾上腺素能生物合成酶多巴胺β-羟化酶(DBH)的基因的启动子,而dHAND可增强Phox2a的活性。在本研究中,我们使用染色质免疫沉淀测定法来鉴定Phox2蛋白和dHAND的靶基因。在SH-SY5Y神经母细胞瘤细胞中,所有这三种蛋白质都与DBH和PHOX2B启动子区域结合。通过荧光各向异性分析Phox2a与dHAND之间的相互作用,结果表明dHAND使Phox2a对其在DBH启动子区域识别位点的亲和力增加了八倍。在编码其他去甲肾上腺素能酶或转运蛋白的基因上未发现Phox2蛋白,但在SH-SY5Y细胞中它们相互结合在彼此的启动子上。与Phox2a和Phox2b一起,dHAND与PHOX2B启动子结合,并且在没有Phox2蛋白的情况下还与GATA2和eHAND基因相关。这些结果证明了去甲肾上腺素能细胞类型中Phox2和dHAND转录因子之间的直接相互作用。发现Phox2蛋白共享所有靶基因,而dHAND独立于Phox2a与基因结合。