Home LiteratureArticle Details
PMID: 10669650 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

New functional promoter polymorphism, CETP/-629, in cholesteryl ester transfer protein (CETP) gene related to CETP mass and high density lipoprotein cholesterol levels: role of Sp1/Sp3 in transcriptional regulation.

Arteriosclerosis, thrombosis, and vascular biology ·Vol. 20 ·No. 2 ·2000-02-00 ·Pages 507-15

Dachet C, Poirier O, Cambien F, Chapman J, Rouis M

Abstract

A new polymorphism located at position -629 (CETP/-629A/C) in the promoter of the cholesteryl ester transfer protein (CETP) gene is described. The -629A allele was associated with lower CETP mass (P<0. 0001) and higher high density lipoprotein cholesterol (P<0.001) than the C allele in a sample of 536 control subjects from the ECTIM study. Transfection studies in HepG2 cells with a luciferase expression vector incorporating a 777-bp fragment of the CETP promoter and containing either A or C at position -629 showed significantly lower luciferase activity with the promoter fragment of the A allele (-25%, P<0.05). By gel-shift assay, DNA-protein interactions were evaluated in nuclear extracts of HepG2 cells with the use of 2 probes (A or C probe) composed of 20 bp of the promoter sequence surrounding the polymorphic site. Two specific complexes of distinct migration rate were identified with the A and the C probe. Competition with an excess of oligonucleotide containing the Sp1 consensus binding site showed that a protein(s) of the Sp transcription factor family was implicated in complex formation with the A probe but not with the C probe. Incubation with specific antibodies indicated that Sp1 and Sp3 bound specifically to the A probe. We introduced mutations in the -629-Sp1 binding site to test its functionality and to define the characteristics of transcription factor binding. We showed, by gel-shift assay, that no nuclear proteins bound to the mutated sequence. Transient transfection of HepG2 cells revealed that the expression of the mutated fragment was significantly increased compared with that of the A promoter fragment (25%, P<0.05). The mutated fragment displayed the same activity as that of the C promoter. These results indicate that Sp1 and/or Sp3 repress CETP promoter activity, whereas nuclear factors binding the C allele are without effect on promoter expression.

MeSH Terms
Adult Binding Sites/physiology Carrier Proteins/blood,genetics,metabolism Cholesterol Ester Transfer Proteins Cholesterol, HDL/blood DNA-Binding Proteins/genetics Electrophoresis, Gel, Two-Dimensional Gene Frequency Glycoproteins Humans Middle Aged Peptide Fragments/metabolism Polymorphism, Genetic/physiology Promoter Regions, Genetic/genetics Sp1 Transcription Factor/genetics,metabolism Sp2 Transcription Factor Transcription Factors/genetics Transcription, Genetic
Chemicals
CETP protein, human Carrier Proteins Cholesterol Ester Transfer Proteins Cholesterol, HDL DNA-Binding Proteins Glycoproteins Peptide Fragments Sp1 Transcription Factor Transcription Factors Sp2 Transcription Factor
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Dachet C
Institut National de la Santé et de la Recherche Médicale (INSERM), Unité 321, Hopital de la Pitié-Salpétrière, Paris, France. cdachet@infobiogen.fr
Poirier O
Cambien F
Chapman J
Rouis M
Article Info
Journal
Arteriosclerosis, thrombosis, and vascular biology
Abbr.
Arterioscler Thromb Vasc Biol
ISSN
1079-5642
Published
2000-02-00
Pages
507-15
Language
English
Region
United States
NLM ID
9505803
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com