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Zebrafish promoter microarrays identify actively transcribed embryonic genes

We have designed a zebrafish genomic microarray to identify DNA-protein interactions in the proximal promoter regions of over 11,000 zebrafish genes. Using these microarrays, together with chromatin immunoprecipitation with an antibody directed against tri-methylated lysine 4 of Histone H3, we demon...

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Autores principales: Wardle, Fiona C, Odom, Duncan T, Bell, George W, Yuan, Bingbing, Danford, Timothy W, Wiellette, Elizabeth L, Herbolsheimer, Elizabeth, Sive, Hazel L, Young, Richard A, Smith, James C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779600/
https://www.ncbi.nlm.nih.gov/pubmed/16889661
http://dx.doi.org/10.1186/gb-2006-7-8-r71
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author Wardle, Fiona C
Odom, Duncan T
Bell, George W
Yuan, Bingbing
Danford, Timothy W
Wiellette, Elizabeth L
Herbolsheimer, Elizabeth
Sive, Hazel L
Young, Richard A
Smith, James C
author_facet Wardle, Fiona C
Odom, Duncan T
Bell, George W
Yuan, Bingbing
Danford, Timothy W
Wiellette, Elizabeth L
Herbolsheimer, Elizabeth
Sive, Hazel L
Young, Richard A
Smith, James C
author_sort Wardle, Fiona C
collection PubMed
description We have designed a zebrafish genomic microarray to identify DNA-protein interactions in the proximal promoter regions of over 11,000 zebrafish genes. Using these microarrays, together with chromatin immunoprecipitation with an antibody directed against tri-methylated lysine 4 of Histone H3, we demonstrate the feasibility of this method in zebrafish. This approach will allow investigators to determine the genomic binding locations of DNA interacting proteins during development and expedite the assembly of the genetic networks that regulate embryogenesis.
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spelling pubmed-17796002007-01-19 Zebrafish promoter microarrays identify actively transcribed embryonic genes Wardle, Fiona C Odom, Duncan T Bell, George W Yuan, Bingbing Danford, Timothy W Wiellette, Elizabeth L Herbolsheimer, Elizabeth Sive, Hazel L Young, Richard A Smith, James C Genome Biol Method We have designed a zebrafish genomic microarray to identify DNA-protein interactions in the proximal promoter regions of over 11,000 zebrafish genes. Using these microarrays, together with chromatin immunoprecipitation with an antibody directed against tri-methylated lysine 4 of Histone H3, we demonstrate the feasibility of this method in zebrafish. This approach will allow investigators to determine the genomic binding locations of DNA interacting proteins during development and expedite the assembly of the genetic networks that regulate embryogenesis. BioMed Central 2006 2006-08-04 /pmc/articles/PMC1779600/ /pubmed/16889661 http://dx.doi.org/10.1186/gb-2006-7-8-r71 Text en Copyright © 2006 Wardle 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
Wardle, Fiona C
Odom, Duncan T
Bell, George W
Yuan, Bingbing
Danford, Timothy W
Wiellette, Elizabeth L
Herbolsheimer, Elizabeth
Sive, Hazel L
Young, Richard A
Smith, James C
Zebrafish promoter microarrays identify actively transcribed embryonic genes
title Zebrafish promoter microarrays identify actively transcribed embryonic genes
title_full Zebrafish promoter microarrays identify actively transcribed embryonic genes
title_fullStr Zebrafish promoter microarrays identify actively transcribed embryonic genes
title_full_unstemmed Zebrafish promoter microarrays identify actively transcribed embryonic genes
title_short Zebrafish promoter microarrays identify actively transcribed embryonic genes
title_sort zebrafish promoter microarrays identify actively transcribed embryonic genes
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779600/
https://www.ncbi.nlm.nih.gov/pubmed/16889661
http://dx.doi.org/10.1186/gb-2006-7-8-r71
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