In vivo analysis of DNA methylation patterns recognized by specific proteins: coupling CHIP and bisulfite analysis

The three-way connection between DNA methylation, chromatin configuration, and transcriptional regulation is under increasing attention, but the fine rules governing the epigenetic control are still poorly understood. In several studies, the authors have concluded that the methylation status of CpG...

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Detalles Bibliográficos
Autores: Matarazzo, Maria Rosaria, Lembo, Francesca, Angrisano, Tiziana, Ballestar Tarín, Esteban, Ferraro, Marcello, Pero, Raffaelo, De Bonis, Maria Luigia, Bruni, C.armelo Bruno, Esteller, Manel, 1968-, D'Esposito, Maurizio, Chiariotti, Lorenzo
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2004
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/219522
Acceso en línea:https://hdl.handle.net/2445/219522
Access Level:acceso abierto
Palabra clave:Cromatina
ADN
Genòmica
Clonatge molecular
Chromatin
DNA
Genomics
Molecular cloning
Descripción
Sumario:The three-way connection between DNA methylation, chromatin configuration, and transcriptional regulation is under increasing attention, but the fine rules governing the epigenetic control are still poorly understood. In several studies, the authors have concluded that the methylation status of CpG sites could be critical for the binding of factors to DNA and, consequently, for chromatin conformation. We tested the possibility that a novel technical approach combining chromatin immunoprecipitation and bisulfite genomic sequencing analysis (ChIP-BA) could provide useful information on the role of specific CpG methylation patterns in driving the association in vivo of proteins to given genomic regions. Our results show that ChIP-BA permits the establishment in vivo of the methylation patterns required for the binding of a methyl-CpG binding protein and, in addition, can potentially identify methylation patterns that do not allow a protein to bind specific genomic regions. Possible fields of application are discussed. We believe that wide use of ChIP-BA could make possible the exploration of a novel aspect of the intricate epigenetic web.