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Sp1 and Sp3 regulate basal transcription of the human APOBEC3G gene

APOBEC3G (A3G), a member of the recently discovered family of human cytidine deaminases, is expressed in peripheral blood lymphocytes and has been shown to be active against HIV-1 and other retroviruses. To gain new insights into the transcriptional regulation of this restriction factor, we cloned a...

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Autores principales: Muckenfuss, Heide, Kaiser, Julia K., Krebil, Erika, Battenberg, Marion, Schwer, Christina, Cichutek, Klaus, Münk, Carsten, Flory, Egbert
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1920263/
https://www.ncbi.nlm.nih.gov/pubmed/17517765
http://dx.doi.org/10.1093/nar/gkm340
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author Muckenfuss, Heide
Kaiser, Julia K.
Krebil, Erika
Battenberg, Marion
Schwer, Christina
Cichutek, Klaus
Münk, Carsten
Flory, Egbert
author_facet Muckenfuss, Heide
Kaiser, Julia K.
Krebil, Erika
Battenberg, Marion
Schwer, Christina
Cichutek, Klaus
Münk, Carsten
Flory, Egbert
author_sort Muckenfuss, Heide
collection PubMed
description APOBEC3G (A3G), a member of the recently discovered family of human cytidine deaminases, is expressed in peripheral blood lymphocytes and has been shown to be active against HIV-1 and other retroviruses. To gain new insights into the transcriptional regulation of this restriction factor, we cloned and characterized the promoter region of A3G. Transcriptional start sites were identified by 5′-rapid amplification of cDNA ends analysis. Luciferase reporter assays demonstrated that a 1025 bp A3G promoter sequence (from −959 to +66 relative to the major transcriptional start site) displayed constitutive promoter activity. In T cells, the A3G promoter was not inducible by mitogenic stimulation, interferon treatment or expression of HIV-1 proteins. Using a series of 5′ deletion promoter constructs in luciferase reporter assays, we identified a 180 bp region that was sufficient for full promoter activity. Transcriptional activity of this A3G core promoter was dependent on a GC-box (located at position −87/−78 relative to the major transcriptional start site) and was abolished after mutation of this DNA element. Electrophoretic mobility shift assays and chromatin immunoprecipitation assays demonstrated that the identified GC-box represented a binding site for the ubiquitous transcription factors specificity protein (Sp) 1 and Sp3.
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spelling pubmed-19202632007-07-19 Sp1 and Sp3 regulate basal transcription of the human APOBEC3G gene Muckenfuss, Heide Kaiser, Julia K. Krebil, Erika Battenberg, Marion Schwer, Christina Cichutek, Klaus Münk, Carsten Flory, Egbert Nucleic Acids Res Molecular Biology APOBEC3G (A3G), a member of the recently discovered family of human cytidine deaminases, is expressed in peripheral blood lymphocytes and has been shown to be active against HIV-1 and other retroviruses. To gain new insights into the transcriptional regulation of this restriction factor, we cloned and characterized the promoter region of A3G. Transcriptional start sites were identified by 5′-rapid amplification of cDNA ends analysis. Luciferase reporter assays demonstrated that a 1025 bp A3G promoter sequence (from −959 to +66 relative to the major transcriptional start site) displayed constitutive promoter activity. In T cells, the A3G promoter was not inducible by mitogenic stimulation, interferon treatment or expression of HIV-1 proteins. Using a series of 5′ deletion promoter constructs in luciferase reporter assays, we identified a 180 bp region that was sufficient for full promoter activity. Transcriptional activity of this A3G core promoter was dependent on a GC-box (located at position −87/−78 relative to the major transcriptional start site) and was abolished after mutation of this DNA element. Electrophoretic mobility shift assays and chromatin immunoprecipitation assays demonstrated that the identified GC-box represented a binding site for the ubiquitous transcription factors specificity protein (Sp) 1 and Sp3. Oxford University Press 2007-06 2007-05-21 /pmc/articles/PMC1920263/ /pubmed/17517765 http://dx.doi.org/10.1093/nar/gkm340 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Muckenfuss, Heide
Kaiser, Julia K.
Krebil, Erika
Battenberg, Marion
Schwer, Christina
Cichutek, Klaus
Münk, Carsten
Flory, Egbert
Sp1 and Sp3 regulate basal transcription of the human APOBEC3G gene
title Sp1 and Sp3 regulate basal transcription of the human APOBEC3G gene
title_full Sp1 and Sp3 regulate basal transcription of the human APOBEC3G gene
title_fullStr Sp1 and Sp3 regulate basal transcription of the human APOBEC3G gene
title_full_unstemmed Sp1 and Sp3 regulate basal transcription of the human APOBEC3G gene
title_short Sp1 and Sp3 regulate basal transcription of the human APOBEC3G gene
title_sort sp1 and sp3 regulate basal transcription of the human apobec3g gene
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1920263/
https://www.ncbi.nlm.nih.gov/pubmed/17517765
http://dx.doi.org/10.1093/nar/gkm340
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