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Hormone-dependent control of developmental timing through regulation of chromatin accessibility
Specification of tissue identity during development requires precise coordination of gene expression in both space and time. Spatially, master regulatory transcription factors are required to control tissue-specific gene expression programs. However, the mechanisms controlling how tissue-specific ge...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458754/ https://www.ncbi.nlm.nih.gov/pubmed/28536147 http://dx.doi.org/10.1101/gad.298182.117 |
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author | Uyehara, Christopher M. Nystrom, Spencer L. Niederhuber, Matthew J. Leatham-Jensen, Mary Ma, Yiqin Buttitta, Laura A. McKay, Daniel J. |
author_facet | Uyehara, Christopher M. Nystrom, Spencer L. Niederhuber, Matthew J. Leatham-Jensen, Mary Ma, Yiqin Buttitta, Laura A. McKay, Daniel J. |
author_sort | Uyehara, Christopher M. |
collection | PubMed |
description | Specification of tissue identity during development requires precise coordination of gene expression in both space and time. Spatially, master regulatory transcription factors are required to control tissue-specific gene expression programs. However, the mechanisms controlling how tissue-specific gene expression changes over time are less well understood. Here, we show that hormone-induced transcription factors control temporal gene expression by regulating the accessibility of DNA regulatory elements. Using the Drosophila wing, we demonstrate that temporal changes in gene expression are accompanied by genome-wide changes in chromatin accessibility at temporal-specific enhancers. We also uncover a temporal cascade of transcription factors following a pulse of the steroid hormone ecdysone such that different times in wing development can be defined by distinct combinations of hormone-induced transcription factors. Finally, we show that the ecdysone-induced transcription factor E93 controls temporal identity by directly regulating chromatin accessibility across the genome. Notably, we found that E93 controls enhancer activity through three different modalities, including promoting accessibility of late-acting enhancers and decreasing accessibility of early-acting enhancers. Together, this work supports a model in which an extrinsic signal triggers an intrinsic transcription factor cascade that drives development forward in time through regulation of chromatin accessibility. |
format | Online Article Text |
id | pubmed-5458754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54587542017-06-16 Hormone-dependent control of developmental timing through regulation of chromatin accessibility Uyehara, Christopher M. Nystrom, Spencer L. Niederhuber, Matthew J. Leatham-Jensen, Mary Ma, Yiqin Buttitta, Laura A. McKay, Daniel J. Genes Dev Research Paper Specification of tissue identity during development requires precise coordination of gene expression in both space and time. Spatially, master regulatory transcription factors are required to control tissue-specific gene expression programs. However, the mechanisms controlling how tissue-specific gene expression changes over time are less well understood. Here, we show that hormone-induced transcription factors control temporal gene expression by regulating the accessibility of DNA regulatory elements. Using the Drosophila wing, we demonstrate that temporal changes in gene expression are accompanied by genome-wide changes in chromatin accessibility at temporal-specific enhancers. We also uncover a temporal cascade of transcription factors following a pulse of the steroid hormone ecdysone such that different times in wing development can be defined by distinct combinations of hormone-induced transcription factors. Finally, we show that the ecdysone-induced transcription factor E93 controls temporal identity by directly regulating chromatin accessibility across the genome. Notably, we found that E93 controls enhancer activity through three different modalities, including promoting accessibility of late-acting enhancers and decreasing accessibility of early-acting enhancers. Together, this work supports a model in which an extrinsic signal triggers an intrinsic transcription factor cascade that drives development forward in time through regulation of chromatin accessibility. Cold Spring Harbor Laboratory Press 2017-05-01 /pmc/articles/PMC5458754/ /pubmed/28536147 http://dx.doi.org/10.1101/gad.298182.117 Text en © 2017 Uyehara et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Paper Uyehara, Christopher M. Nystrom, Spencer L. Niederhuber, Matthew J. Leatham-Jensen, Mary Ma, Yiqin Buttitta, Laura A. McKay, Daniel J. Hormone-dependent control of developmental timing through regulation of chromatin accessibility |
title | Hormone-dependent control of developmental timing through regulation of chromatin accessibility |
title_full | Hormone-dependent control of developmental timing through regulation of chromatin accessibility |
title_fullStr | Hormone-dependent control of developmental timing through regulation of chromatin accessibility |
title_full_unstemmed | Hormone-dependent control of developmental timing through regulation of chromatin accessibility |
title_short | Hormone-dependent control of developmental timing through regulation of chromatin accessibility |
title_sort | hormone-dependent control of developmental timing through regulation of chromatin accessibility |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458754/ https://www.ncbi.nlm.nih.gov/pubmed/28536147 http://dx.doi.org/10.1101/gad.298182.117 |
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