Yatsunami K, Fukui T, Ichikawa A
Japan Tobacco Inc., Pharmaceutical Basic Research Laboratories, Yokohama.
Yakugaku Zasshi. 1994 Nov;114(11):803-22. doi: 10.1248/yakushi1947.114.11_803.
L-Histidine decarboxylase (HDC) catalyzes the formation of histamine from L-histidine. This biogenic amine is known to exert various effects in physiological and pathological reactions. In contrast to the well-known mechanism of histamine action through its interaction with specific receptors, the mechanisms regulating HDC gene expression are not elucidated. We have purified HDC from mouse mastocytoma cells, and isolated mouse HDC cDNA, and found that the primary translated product is posttranslationally processed to yield a mature active enzyme. In mastocytoma cells, we demonstrated that the induction of HDC activity and HDC mRNA synergistically occurred on treatment with dexamethasone+TPA, and also cAMP+Ca2+. To clarify the mechanism of up-regulation by these stimuli of the transcription of the HDC gene, we have isolated a genomic DNA clone encoding 5'-flanking region sequence and the first two exons. The transcription start site and the nucleotide sequences of the promoter regions including TATA- and GC-boxes were determined. With mastocytoma cells transiently transfected with 5' deletion constructs of HDC-CAT fusion gene, it was found that the sequences from -132 to -53 and -267 to -53 are essential for the regulatory elements involved in the increased transcription of the HDC gene with dexamethasone+TPA and cAMP+Ca2+, respectively. Furthermore, we have isolated a genomic DNA from human basophilic cells, and analysed its structure to elucidate the mechanisms regulating the tissue specificity of HDC gene expression.
L-组氨酸脱羧酶(HDC)催化L-组氨酸生成组胺。已知这种生物胺在生理和病理反应中发挥多种作用。与通过与特定受体相互作用的组胺作用的知名机制不同,调节HDC基因表达的机制尚未阐明。我们从小鼠肥大细胞瘤细胞中纯化了HDC,并分离出小鼠HDC cDNA,发现初级翻译产物经过翻译后加工产生成熟的活性酶。在肥大细胞瘤细胞中,我们证明用地塞米松+佛波酯(TPA)以及cAMP+Ca2+处理后,HDC活性和HDC mRNA的诱导协同发生。为了阐明这些刺激上调HDC基因转录的机制,我们分离出了一个编码5'侧翼区域序列和前两个外显子的基因组DNA克隆。确定了转录起始位点以及包括TATA盒和GC盒在内的启动子区域的核苷酸序列。用HDC-CAT融合基因的5'缺失构建体瞬时转染肥大细胞瘤细胞后发现,-132至-53和-267至-53的序列分别对于地塞米松+TPA和cAMP+Ca2+增加HDC基因转录所涉及的调控元件至关重要。此外,我们从人嗜碱性细胞中分离出基因组DNA,并分析其结构以阐明调节HDC基因表达组织特异性的机制。