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[L-组氨酸脱羧酶的分子生物学]

[Molecular biology of L-histidine decarboxylase].

作者信息

Yatsunami K, Fukui T, Ichikawa A

机构信息

Japan Tobacco Inc., Pharmaceutical Basic Research Laboratories, Yokohama.

出版信息

Yakugaku Zasshi. 1994 Nov;114(11):803-22. doi: 10.1248/yakushi1947.114.11_803.

DOI:10.1248/yakushi1947.114.11_803
PMID:7853145
Abstract

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.

摘要

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。

相似文献

1
[Molecular biology of L-histidine decarboxylase].[L-组氨酸脱羧酶的分子生物学]
Yakugaku Zasshi. 1994 Nov;114(11):803-22. doi: 10.1248/yakushi1947.114.11_803.
2
Enhanced expression of the mouse L-histidine decarboxylase gene with a combination of dexamethasone and 12-O-tetradecanoylphorbol-13-acetate.
Biochem Biophys Res Commun. 1993 Nov 15;196(3):1113-9. doi: 10.1006/bbrc.1993.2366.
3
De Novo synthesis and posttranslational processing of L-histidine decarboxylase in mice.
Methods Find Exp Clin Pharmacol. 1995 Nov;17 Suppl C:5-9.
4
cDNA-derived amino acid sequence of L-histidine decarboxylase from mouse mastocytoma P-815 cells.
FEBS Lett. 1990 Dec 10;276(1-2):214-8. doi: 10.1016/0014-5793(90)80545-t.
5
The mouse L-histidine decarboxylase gene: structure and transcriptional regulation by CpG methylation in the promoter region.小鼠L-组氨酸脱羧酶基因:启动子区域的结构及CpG甲基化对其转录的调控
Nucleic Acids Res. 2000 Jul 15;28(14):2627-33. doi: 10.1093/nar/28.14.2627.
6
Structure of the L-histidine decarboxylase gene.
J Biol Chem. 1994 Jan 14;269(2):1554-9.
7
Synergistic effects of cyclic AMP and Ca2+ ionophore A23187 on de novo synthesis of histidine decarboxylase in mastocytoma P-815 cells.
Biochim Biophys Acta. 1992 Jan 13;1133(2):179-86. doi: 10.1016/0167-4889(92)90067-l.
8
Rat histidine decarboxylase promoter is regulated by gastrin through a protein kinase C pathway.大鼠组氨酸脱羧酶启动子受胃泌素通过蛋白激酶C途径调控。
Am J Physiol. 1996 Apr;270(4 Pt 1):G619-33. doi: 10.1152/ajpgi.1996.270.4.G619.
9
Cloning of the cDNA encoding human histidine decarboxylase from an erythroleukemia cell line and mapping of the gene locus to chromosome 15.
DNA Seq. 1991;1(6):395-400. doi: 10.3109/10425179109020795.
10
Mast cell-/basophil-specific transcriptional regulation of human L-histidine decarboxylase gene by CpG methylation in the promoter region.启动子区域CpG甲基化对人L-组氨酸脱羧酶基因的肥大细胞/嗜碱性粒细胞特异性转录调控
J Biol Chem. 1998 Nov 20;273(47):31607-14. doi: 10.1074/jbc.273.47.31607.

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