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Divergent Regulation of the Growth-promoting Gene IEX-1 by the P53 Tumor Suppressor and Sp1

Overview
Journal J Biol Chem
Specialty Biochemistry
Date 2002 Feb 15
PMID 11844788
Citations 19
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Abstract

IEX-1, a recently discovered early response gene, regulates cell growth and apoptosis. IEX-1 gene expression is regulated by a variety of factors such as x-irradiation, ultraviolet radiation, steroids, growth factors, and inflammatory stimuli. By systematic examination of the IEX-1 promoter, we show that IEX-1 gene expression is controlled by multiple conserved gene regulatory elements and that IEX-1 is a downstream target of the p53 tumor suppressor and Sp1. In addition, p300, Sox, nuclear factor-kappaB, and AP4 appear to be modulators of IEX-1 gene expression to a lesser degree. We found that there is at least one Sp1 element that functions as an activator and contributes to high basal transcriptional levels of the IEX-1 gene. We demonstrate the presence of a p53 response element that represses IEX-1 promoter activity in HaCaT keratinocytes, indicating that Sp1 and p53 have opposite effects on IEX-1 gene expression. We conclude that IEX-1 expression in cells is regulated by the p53 tumor suppressor and Sp1, thus providing a direct mechanism for control of cell proliferation.

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References
1.
Schafer H, Diebel J, Arlt A, Trauzold A, Schmidt W . The promoter of human p22/PACAP response gene 1 (PRG1) contains functional binding sites for the p53 tumor suppressor and for NFkappaB. FEBS Lett. 1998; 436(2):139-43. DOI: 10.1016/s0014-5793(98)01109-0. View

2.
Kumar R, Kobayashi T, Warner G, Wu Y, Salisbury J, Lingle W . A novel immediate early response gene, IEX-1, is induced by ultraviolet radiation in human keratinocytes. Biochem Biophys Res Commun. 1999; 253(2):336-41. DOI: 10.1006/bbrc.1998.9692. View

3.
Hagen G, Muller S, Beato M, Suske G . Sp1-mediated transcriptional activation is repressed by Sp3. EMBO J. 1994; 13(16):3843-51. PMC: 395297. DOI: 10.1002/j.1460-2075.1994.tb06695.x. View

4.
Schafer H, Trauzold A, Sebens T, Deppert W, Folsch U, Schmidt W . The proliferation-associated early response gene p22/PRG1 is a novel p53 target gene. Oncogene. 1998; 16(19):2479-87. DOI: 10.1038/sj.onc.1201788. View

5.
Huang L, Sowa Y, Sakai T, Pardee A . Activation of the p21WAF1/CIP1 promoter independent of p53 by the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) through the Sp1 sites. Oncogene. 2000; 19(50):5712-9. DOI: 10.1038/sj.onc.1203963. View