cDNA cloning and gene expression analysis of human myo-inositol 1-phosphate synthase

被引:40
|
作者
Guan, GM [1 ]
Dai, PH [1 ]
Shechter, I [1 ]
机构
[1] Uniformed Serv Univ Hlth Sci, F Edward Herbert Sch Med, Dept Surg, Bethesda, MD 20814 USA
关键词
myo-Inositol; myo-Inositol 1-phosphate synthase; gene expression; transcriptional regulation; G-proteins;
D O I
10.1016/S0003-9861(03)00388-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
myo-Inositol 1-phosphate synthase (EC 5.5.1.4) (IPS) is a key enzyme in myo-inositol biosynthesis pathway. This study describes the molecular cloning of the full length human myo-inositol 1-phosphate synthase (hIPS) cDNA, tissue distribution of its mRNA and characterizes its gene expression in cultured HepG2 cells. Human testis, ovary, heart, placenta, and pancreas express relatively high level of hIPS mRNA, while blood leukocyte, thymus, skeletal muscle, and colon express low or marginal amount of the mRNA. In the presence of glucose, hIPS mRNA level increases 2- to 4-fold in HepG2 cells. hIPS mRNA is also up-regulated 2- to 3-fold by 2.5 muM lovastain. This up-regulation is prevented by mevalonic acid, farnesol, and geranylgeraniol, suggesting a G-protein mediated signal transduction mechanism in the regulation of hIPS gene expression. hIPS mRNA expression is 50% suppressed by 10 mM lithium ion in these cells. Neither 5 mM myo-inositol nor the three hormones: estrogen, thyroid hormone, and insulin altered hIPS mRNA expression in these cells. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:251 / 259
页数:9
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