Shimojo M, Wu D, Hersh L B
Department of Biochemistry, University of Kentucky, Lexington 40536-0084, USA.
J Neurochem. 1998 Sep;71(3):1118-26. doi: 10.1046/j.1471-4159.1998.71031118.x.
The vesicular acetylcholine transporter (VAChT) gene and the choline acetyltransferase (ChAT) gene comprise the cholinergic gene locus. We have studied the coordinate regulation of these genes by cyclic AMP-dependent protein kinase (PKA) in the rat pheochromocytoma cell line PC12 and PC12 PKA-deficient mutants. Both ChAT and VAChT mRNA increased approximately fourfold after treatment of PC12 cells with dibutyryl cyclic AMP (dbcAMP). ChAT and PKA activity were also increased by dbcAMP. The basal levels of ChAT and VAChT mRNAs in the PKA-deficient cell lines were both about six times lower than in wild-type PC12 cells, and were induced less than twofold by addition of dbcAMP. H-89 and H-9, specific inhibitors for PKA, reduced ChAT and VAChT mRNA levels to approximately one-third that of untreated cells and ChAT activity to approximately one-fourth that of untreated PC12 cells. Activation of PKA type II, but not PKA type I, increased ChAT activity approximately threefold. Analysis of reporter gene constructs indicates that PKA affects gene transcription at an upstream site in the cholinergic gene locus. These results demonstrate that the expression of the ChAT and VAChT genes is regulated coordinately at the transcriptional level, and a signaling pathway specifically involving PKA II plays an important role in this process.
囊泡乙酰胆碱转运体(VAChT)基因和胆碱乙酰转移酶(ChAT)基因构成胆碱能基因位点。我们已经在大鼠嗜铬细胞瘤细胞系PC12和PC12 PKA缺陷型突变体中研究了环磷酸腺苷依赖性蛋白激酶(PKA)对这些基因的协同调控。用二丁酰环磷酸腺苷(dbcAMP)处理PC12细胞后,ChAT和VAChT mRNA均增加了约四倍。dbcAMP也增加了ChAT和PKA的活性。PKA缺陷型细胞系中ChAT和VAChT mRNA的基础水平均比野生型PC12细胞低约六倍,并且添加dbcAMP后诱导增加不到两倍。PKA的特异性抑制剂H-89和H-9将ChAT和VAChT mRNA水平降低至未处理细胞的约三分之一,将ChAT活性降低至未处理PC12细胞的约四分之一。II型PKA的激活而非I型PKA的激活使ChAT活性增加了约三倍。报告基因构建体的分析表明,PKA在胆碱能基因位点的上游位点影响基因转录。这些结果表明,ChAT和VAChT基因的表达在转录水平上受到协同调控,并且一条特别涉及PKA II的信号通路在这一过程中起重要作用。