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Dynamic reprogramming of chromatin accessibility during Drosophila embryo development

BACKGROUND: The development of complex organisms is believed to involve progressive restrictions in cellular fate. Understanding the scope and features of chromatin dynamics during embryogenesis, and identifying regulatory elements important for directing developmental processes remain key goals of...

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Autores principales: Thomas, Sean, Li, Xiao-Yong, Sabo, Peter J, Sandstrom, Richard, Thurman, Robert E, Canfield, Theresa K, Giste, Erika, Fisher, William, Hammonds, Ann, Celniker, Susan E, Biggin, Mark D, Stamatoyannopoulos, John A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219966/
https://www.ncbi.nlm.nih.gov/pubmed/21569360
http://dx.doi.org/10.1186/gb-2011-12-5-r43
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author Thomas, Sean
Li, Xiao-Yong
Sabo, Peter J
Sandstrom, Richard
Thurman, Robert E
Canfield, Theresa K
Giste, Erika
Fisher, William
Hammonds, Ann
Celniker, Susan E
Biggin, Mark D
Stamatoyannopoulos, John A
author_facet Thomas, Sean
Li, Xiao-Yong
Sabo, Peter J
Sandstrom, Richard
Thurman, Robert E
Canfield, Theresa K
Giste, Erika
Fisher, William
Hammonds, Ann
Celniker, Susan E
Biggin, Mark D
Stamatoyannopoulos, John A
author_sort Thomas, Sean
collection PubMed
description BACKGROUND: The development of complex organisms is believed to involve progressive restrictions in cellular fate. Understanding the scope and features of chromatin dynamics during embryogenesis, and identifying regulatory elements important for directing developmental processes remain key goals of developmental biology. RESULTS: We used in vivo DNaseI sensitivity to map the locations of regulatory elements, and explore the changing chromatin landscape during the first 11 hours of Drosophila embryonic development. We identified thousands of conserved, developmentally dynamic, distal DNaseI hypersensitive sites associated with spatial and temporal expression patterning of linked genes and with large regions of chromatin plasticity. We observed a nearly uniform balance between developmentally up- and down-regulated DNaseI hypersensitive sites. Analysis of promoter chromatin architecture revealed a novel role for classical core promoter sequence elements in directing temporally regulated chromatin remodeling. Another unexpected feature of the chromatin landscape was the presence of localized accessibility over many protein-coding regions, subsets of which were developmentally regulated or associated with the transcription of genes with prominent maternal RNA contributions in the blastoderm. CONCLUSIONS: Our results provide a global view of the rich and dynamic chromatin landscape of early animal development, as well as novel insights into the organization of developmentally regulated chromatin features.
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spelling pubmed-32199662011-11-18 Dynamic reprogramming of chromatin accessibility during Drosophila embryo development Thomas, Sean Li, Xiao-Yong Sabo, Peter J Sandstrom, Richard Thurman, Robert E Canfield, Theresa K Giste, Erika Fisher, William Hammonds, Ann Celniker, Susan E Biggin, Mark D Stamatoyannopoulos, John A Genome Biol Research BACKGROUND: The development of complex organisms is believed to involve progressive restrictions in cellular fate. Understanding the scope and features of chromatin dynamics during embryogenesis, and identifying regulatory elements important for directing developmental processes remain key goals of developmental biology. RESULTS: We used in vivo DNaseI sensitivity to map the locations of regulatory elements, and explore the changing chromatin landscape during the first 11 hours of Drosophila embryonic development. We identified thousands of conserved, developmentally dynamic, distal DNaseI hypersensitive sites associated with spatial and temporal expression patterning of linked genes and with large regions of chromatin plasticity. We observed a nearly uniform balance between developmentally up- and down-regulated DNaseI hypersensitive sites. Analysis of promoter chromatin architecture revealed a novel role for classical core promoter sequence elements in directing temporally regulated chromatin remodeling. Another unexpected feature of the chromatin landscape was the presence of localized accessibility over many protein-coding regions, subsets of which were developmentally regulated or associated with the transcription of genes with prominent maternal RNA contributions in the blastoderm. CONCLUSIONS: Our results provide a global view of the rich and dynamic chromatin landscape of early animal development, as well as novel insights into the organization of developmentally regulated chromatin features. BioMed Central 2011 2011-05-11 /pmc/articles/PMC3219966/ /pubmed/21569360 http://dx.doi.org/10.1186/gb-2011-12-5-r43 Text en Copyright ©2011 Thomas 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 Research
Thomas, Sean
Li, Xiao-Yong
Sabo, Peter J
Sandstrom, Richard
Thurman, Robert E
Canfield, Theresa K
Giste, Erika
Fisher, William
Hammonds, Ann
Celniker, Susan E
Biggin, Mark D
Stamatoyannopoulos, John A
Dynamic reprogramming of chromatin accessibility during Drosophila embryo development
title Dynamic reprogramming of chromatin accessibility during Drosophila embryo development
title_full Dynamic reprogramming of chromatin accessibility during Drosophila embryo development
title_fullStr Dynamic reprogramming of chromatin accessibility during Drosophila embryo development
title_full_unstemmed Dynamic reprogramming of chromatin accessibility during Drosophila embryo development
title_short Dynamic reprogramming of chromatin accessibility during Drosophila embryo development
title_sort dynamic reprogramming of chromatin accessibility during drosophila embryo development
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219966/
https://www.ncbi.nlm.nih.gov/pubmed/21569360
http://dx.doi.org/10.1186/gb-2011-12-5-r43
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