Protein-Binding Microarray Analysis of Tumor Suppressor AP2α Target Gene Specificity.

Détails

Ressource 1Télécharger: BIB_279EFB4814CA.P001.pdf (1081.56 [Ko])
Etat: Public
Version: Final published version
ID Serval
serval:BIB_279EFB4814CA
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Protein-Binding Microarray Analysis of Tumor Suppressor AP2α Target Gene Specificity.
Périodique
Plos One
Auteur(s)
Kerschgens J., Renaud S., Schütz F., Grasso L., Egener-Kuhn T., Delaloye J.F., Lehr H.A., Vogel H., Mermod N.
ISSN
1932-6203 (Electronic)
ISSN-L
1932-6203
Statut éditorial
Publié
Date de publication
2011
Volume
6
Numéro
8
Pages
e22895
Langue
anglais
Résumé
Cheap and massively parallel methods to assess the DNA-binding specificity of transcription factors are actively sought, given their prominent regulatory role in cellular processes and diseases. Here we evaluated the use of protein-binding microarrays (PBM) to probe the association of the tumor suppressor AP2α with 6000 human genomic DNA regulatory sequences. We show that the PBM provides accurate relative binding affinities when compared to quantitative surface plasmon resonance assays. A PBM-based study of human healthy and breast tumor tissue extracts allowed the identification of previously unknown AP2α target genes and it revealed genes whose direct or indirect interactions with AP2α are affected in the diseased tissues. AP2α binding and regulation was confirmed experimentally in human carcinoma cells for novel target genes involved in tumor progression and resistance to chemotherapeutics, providing a molecular interpretation of AP2α role in cancer chemoresistance. Overall, we conclude that this approach provides quantitative and accurate assays of the specificity and activity of tumor suppressor and oncogenic proteins in clinical samples, interfacing genomic and proteomic assays.
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/02/2011 11:26
Dernière modification de la notice
20/08/2019 13:06
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