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Development of an Illumina-based ChIP-exonuclease method provides insight into FoxA1-DNA binding properties

ChIP-exonuclease (ChIP-exo) is a modified ChIP-seq approach for high resolution mapping of transcription factor DNA sites. We describe an Illumina-based ChIP-exo method which provides a global improvement of the data quality of estrogen receptor (ER) ChIP and insights into the motif structure for ke...

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Detalles Bibliográficos
Autores principales: Serandour, Aurelien A, Brown, Gordon D, Cohen, Joshua D, Carroll, Jason S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053927/
https://www.ncbi.nlm.nih.gov/pubmed/24373287
http://dx.doi.org/10.1186/gb-2013-14-12-r147
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author Serandour, Aurelien A
Brown, Gordon D
Cohen, Joshua D
Carroll, Jason S
author_facet Serandour, Aurelien A
Brown, Gordon D
Cohen, Joshua D
Carroll, Jason S
author_sort Serandour, Aurelien A
collection PubMed
description ChIP-exonuclease (ChIP-exo) is a modified ChIP-seq approach for high resolution mapping of transcription factor DNA sites. We describe an Illumina-based ChIP-exo method which provides a global improvement of the data quality of estrogen receptor (ER) ChIP and insights into the motif structure for key ER-associated factors. ChIP-exo of the ER pioneer factor FoxA1 identifies protected DNA with a predictable 8 bp overhang from the Forkhead motif, which we term mesas. We show that mesas occur in multiple cellular contexts and exist as single or overlapping motifs. Our Illumina-based ChIP-exo provides high resolution mapping of transcription factor binding sites.
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spelling pubmed-40539272014-06-12 Development of an Illumina-based ChIP-exonuclease method provides insight into FoxA1-DNA binding properties Serandour, Aurelien A Brown, Gordon D Cohen, Joshua D Carroll, Jason S Genome Biol Method ChIP-exonuclease (ChIP-exo) is a modified ChIP-seq approach for high resolution mapping of transcription factor DNA sites. We describe an Illumina-based ChIP-exo method which provides a global improvement of the data quality of estrogen receptor (ER) ChIP and insights into the motif structure for key ER-associated factors. ChIP-exo of the ER pioneer factor FoxA1 identifies protected DNA with a predictable 8 bp overhang from the Forkhead motif, which we term mesas. We show that mesas occur in multiple cellular contexts and exist as single or overlapping motifs. Our Illumina-based ChIP-exo provides high resolution mapping of transcription factor binding sites. BioMed Central 2013 2013-12-27 /pmc/articles/PMC4053927/ /pubmed/24373287 http://dx.doi.org/10.1186/gb-2013-14-12-r147 Text en Copyright © 2013 Serandour et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Method
Serandour, Aurelien A
Brown, Gordon D
Cohen, Joshua D
Carroll, Jason S
Development of an Illumina-based ChIP-exonuclease method provides insight into FoxA1-DNA binding properties
title Development of an Illumina-based ChIP-exonuclease method provides insight into FoxA1-DNA binding properties
title_full Development of an Illumina-based ChIP-exonuclease method provides insight into FoxA1-DNA binding properties
title_fullStr Development of an Illumina-based ChIP-exonuclease method provides insight into FoxA1-DNA binding properties
title_full_unstemmed Development of an Illumina-based ChIP-exonuclease method provides insight into FoxA1-DNA binding properties
title_short Development of an Illumina-based ChIP-exonuclease method provides insight into FoxA1-DNA binding properties
title_sort development of an illumina-based chip-exonuclease method provides insight into foxa1-dna binding properties
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053927/
https://www.ncbi.nlm.nih.gov/pubmed/24373287
http://dx.doi.org/10.1186/gb-2013-14-12-r147
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