E2F1 regulation of the human myo-inositol 1-phosphate synthase (ISYNA1) gene promoter

被引:15
|
作者
Seelan, RS
Parthasarathy, LK
Parthasarathy, RN [1 ]
机构
[1] VA Med Ctr, Mol Neurosci & Bioinformat Labs, Mental Hlth Behav Sci & Res Serv, Louisville, KY 40206 USA
[2] Univ Louisville, Hlth Sci Ctr, Dept Psychiat, Louisville, KY 40202 USA
[3] Univ Louisville, Hlth Sci Ctr, Dept Biochem, Louisville, KY 40202 USA
[4] Univ Louisville, Hlth Sci Ctr, Dept Mol Biol, Louisville, KY 40202 USA
关键词
E2F1; INO1; inositol; ISYNA1; lithium; myo-inositol 1-phosphate synthase; valproate;
D O I
10.1016/j.abb.2004.08.002
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
Human niyo-inositol 1-phosphate synthase (IP synthase; E.C. 5.5.1.4), encoded by ISYNA1, catalyzes the de novo synthesis of inositol 1-phosphate from glucose 6-phosphate. It is a potential target for mood-stabilizing drugs such as lithium and valproate. But, very little is known about the regulation of human IP synthase. Here, we have characterized the minimal promoter of ISYNA1 and show that it is upregulated by E2F1. Upregulation occurs in a dose-dependent fashion and can be suppressed by ectopic expression of Rb. EMSA and antibody supershift analysis identified a functional E2F binding motif at -117. Complex formation at this site was competed by an excess of unlabeled Sp1 oligo consistent with the -117 E2F site overlapping an Sp1 motif. Because the -117 E2F motif is not a high-affinity binding site, we propose that the upregulation of ISYNA1 occurs through the cooperative interaction of several low-affinity E2F binding motifs present in the minimal promoter. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:95 / 106
页数:12
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