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Mapping and Dynamics of Regulatory DNA in Maturing Arabidopsis thaliana Siliques

The genome is reprogrammed during development to produce diverse cell types, largely through altered expression and activity of key transcription factors. The accessibility and critical functions of epidermal cells have made them a model for connecting transcriptional events to development in a rang...

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Autores principales: Sullivan, Alessandra M., Arsovski, Andrej A., Thompson, Agnieszka, Sandstrom, Richard, Thurman, Robert E., Neph, Shane, Johnson, Audra K., Sullivan, Shawn T., Sabo, Peter J., Neri, Fidencio V., Weaver, Molly, Diegel, Morgan, Nemhauser, Jennifer L., Stamatoyannopoulos, John A., Bubb, Kerry L., Queitsch, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868056/
https://www.ncbi.nlm.nih.gov/pubmed/31798605
http://dx.doi.org/10.3389/fpls.2019.01434
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author Sullivan, Alessandra M.
Arsovski, Andrej A.
Thompson, Agnieszka
Sandstrom, Richard
Thurman, Robert E.
Neph, Shane
Johnson, Audra K.
Sullivan, Shawn T.
Sabo, Peter J.
Neri, Fidencio V.
Weaver, Molly
Diegel, Morgan
Nemhauser, Jennifer L.
Stamatoyannopoulos, John A.
Bubb, Kerry L.
Queitsch, Christine
author_facet Sullivan, Alessandra M.
Arsovski, Andrej A.
Thompson, Agnieszka
Sandstrom, Richard
Thurman, Robert E.
Neph, Shane
Johnson, Audra K.
Sullivan, Shawn T.
Sabo, Peter J.
Neri, Fidencio V.
Weaver, Molly
Diegel, Morgan
Nemhauser, Jennifer L.
Stamatoyannopoulos, John A.
Bubb, Kerry L.
Queitsch, Christine
author_sort Sullivan, Alessandra M.
collection PubMed
description The genome is reprogrammed during development to produce diverse cell types, largely through altered expression and activity of key transcription factors. The accessibility and critical functions of epidermal cells have made them a model for connecting transcriptional events to development in a range of model systems. In Arabidopsis thaliana and many other plants, fertilization triggers differentiation of specialized epidermal seed coat cells that have a unique morphology caused by large extracellular deposits of polysaccharides. Here, we used DNase I-seq to generate regulatory landscapes of A. thaliana seeds at two critical time points in seed coat maturation (4 and 7 DPA), enriching for seed coat cells with the INTACT method. We found over 3,000 developmentally dynamic regulatory DNA elements and explored their relationship with nearby gene expression. The dynamic regulatory elements were enriched for motifs for several transcription factors families; most notably the TCP family at the earlier time point and the MYB family at the later one. To assess the extent to which the observed regulatory sites in seeds added to previously known regulatory sites in A. thaliana, we compared our data to 11 other data sets generated with 7-day-old seedlings for diverse tissues and conditions. Surprisingly, over a quarter of the regulatory, i.e. accessible, bases observed in seeds were novel. Notably, plant regulatory landscapes from different tissues, cell types, or developmental stages were more dynamic than those generated from bulk tissue in response to environmental perturbations, highlighting the importance of extending studies of regulatory DNA to single tissues and cell types during development.
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spelling pubmed-68680562019-12-03 Mapping and Dynamics of Regulatory DNA in Maturing Arabidopsis thaliana Siliques Sullivan, Alessandra M. Arsovski, Andrej A. Thompson, Agnieszka Sandstrom, Richard Thurman, Robert E. Neph, Shane Johnson, Audra K. Sullivan, Shawn T. Sabo, Peter J. Neri, Fidencio V. Weaver, Molly Diegel, Morgan Nemhauser, Jennifer L. Stamatoyannopoulos, John A. Bubb, Kerry L. Queitsch, Christine Front Plant Sci Plant Science The genome is reprogrammed during development to produce diverse cell types, largely through altered expression and activity of key transcription factors. The accessibility and critical functions of epidermal cells have made them a model for connecting transcriptional events to development in a range of model systems. In Arabidopsis thaliana and many other plants, fertilization triggers differentiation of specialized epidermal seed coat cells that have a unique morphology caused by large extracellular deposits of polysaccharides. Here, we used DNase I-seq to generate regulatory landscapes of A. thaliana seeds at two critical time points in seed coat maturation (4 and 7 DPA), enriching for seed coat cells with the INTACT method. We found over 3,000 developmentally dynamic regulatory DNA elements and explored their relationship with nearby gene expression. The dynamic regulatory elements were enriched for motifs for several transcription factors families; most notably the TCP family at the earlier time point and the MYB family at the later one. To assess the extent to which the observed regulatory sites in seeds added to previously known regulatory sites in A. thaliana, we compared our data to 11 other data sets generated with 7-day-old seedlings for diverse tissues and conditions. Surprisingly, over a quarter of the regulatory, i.e. accessible, bases observed in seeds were novel. Notably, plant regulatory landscapes from different tissues, cell types, or developmental stages were more dynamic than those generated from bulk tissue in response to environmental perturbations, highlighting the importance of extending studies of regulatory DNA to single tissues and cell types during development. Frontiers Media S.A. 2019-11-14 /pmc/articles/PMC6868056/ /pubmed/31798605 http://dx.doi.org/10.3389/fpls.2019.01434 Text en Copyright © 2019 Sullivan, Arsovski, Thompson, Sandstrom, Thurman, Neph, Johnson, Sullivan, Sabo, Neri, Weaver, Diegel, Nemhauser, Stamatoyannopoulos, Bubb and Queitsch http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Sullivan, Alessandra M.
Arsovski, Andrej A.
Thompson, Agnieszka
Sandstrom, Richard
Thurman, Robert E.
Neph, Shane
Johnson, Audra K.
Sullivan, Shawn T.
Sabo, Peter J.
Neri, Fidencio V.
Weaver, Molly
Diegel, Morgan
Nemhauser, Jennifer L.
Stamatoyannopoulos, John A.
Bubb, Kerry L.
Queitsch, Christine
Mapping and Dynamics of Regulatory DNA in Maturing Arabidopsis thaliana Siliques
title Mapping and Dynamics of Regulatory DNA in Maturing Arabidopsis thaliana Siliques
title_full Mapping and Dynamics of Regulatory DNA in Maturing Arabidopsis thaliana Siliques
title_fullStr Mapping and Dynamics of Regulatory DNA in Maturing Arabidopsis thaliana Siliques
title_full_unstemmed Mapping and Dynamics of Regulatory DNA in Maturing Arabidopsis thaliana Siliques
title_short Mapping and Dynamics of Regulatory DNA in Maturing Arabidopsis thaliana Siliques
title_sort mapping and dynamics of regulatory dna in maturing arabidopsis thaliana siliques
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868056/
https://www.ncbi.nlm.nih.gov/pubmed/31798605
http://dx.doi.org/10.3389/fpls.2019.01434
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