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In vitro and in vivo effects of a multimerized ?s1-casein enhancer on whey acidic protein gene promoter activity

Authors :
Celeste Menck-Le Bourhis
Thais Pantano
Geneviève Jolivet
Sonia Prince
Sylvie Rival-Gervier
Caroline Maeder
Louis-Marie Houdebine
Celine Viglietta
Biologie du développement et reproduction (BDR)
Centre National de la Recherche Scientifique (CNRS)-École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)
Source :
Molecular Reproduction and Development, Molecular Reproduction and Development, Wiley, 2003, 65, pp.262-268, HAL
Publication Year :
2003
Publisher :
Wiley, 2003.

Abstract

Experimental data obtained in previous works have led to postulate that enhancers increase the frequency of action of a linked promoter in a given cell and may have some insulating effects. The multimerized rabbit alpha s1-casein gene enhancer, the 6i multimer, was added upstream of the rabbit whey acidic protein gene (WAP) promoter (-6,300; +28 bp) fused to the firefly luciferase (luc) gene (6i WAP-luc construct). The 6i multimer increased reporter gene expression in mouse mammary HC11 cells. In transgenic mice, a very weak but significant increase was also observed. More noticeable, no silent lines were found when the 6i multimer was associated to the WAP-luc construct. This reflects the fact that the 6i multimer tends to prevent the silencing of the WAP-luc construct. After addition of the 5'HS4 insulator region from the chicken beta-globin locus upstream of the 6i multimer, similar luciferase levels were measured in 6i WAP-luc and 5'HS4 WAP-luc transgenic mice. Our present data and previous ones, which show that the 6i multimer has no insulating activity on a TK gene promoter construct indicate that the insulating activity of the 6i multimer is construct-dependent and not amplified by the 5'HS4 insulator.

Details

ISSN :
10982795 and 1040452X
Volume :
65
Database :
OpenAIRE
Journal :
Molecular Reproduction and Development
Accession number :
edsair.doi.dedup.....2b1a12aebf160103ddaa7c0e74c45c79
Full Text :
https://doi.org/10.1002/mrd.10302