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Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity
Developmental enhancers integrate graded concentrations of transcription factors (TFs) to create sharp gene expression boundaries. Here we examine the hunchback P2 (HbP2) enhancer which drives a sharp expression pattern in the Drosophila blastoderm embryo in response to the transcriptional activator...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588347/ https://www.ncbi.nlm.nih.gov/pubmed/31223115 http://dx.doi.org/10.7554/eLife.41266 |
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author | Park, Jeehae Estrada, Javier Johnson, Gemma Vincent, Ben J Ricci-Tam, Chiara Bragdon, Meghan DJ Shulgina, Yekaterina Cha, Anna Wunderlich, Zeba Gunawardena, Jeremy DePace, Angela H |
author_facet | Park, Jeehae Estrada, Javier Johnson, Gemma Vincent, Ben J Ricci-Tam, Chiara Bragdon, Meghan DJ Shulgina, Yekaterina Cha, Anna Wunderlich, Zeba Gunawardena, Jeremy DePace, Angela H |
author_sort | Park, Jeehae |
collection | PubMed |
description | Developmental enhancers integrate graded concentrations of transcription factors (TFs) to create sharp gene expression boundaries. Here we examine the hunchback P2 (HbP2) enhancer which drives a sharp expression pattern in the Drosophila blastoderm embryo in response to the transcriptional activator Bicoid (Bcd). We systematically interrogate cis and trans factors that influence the shape and position of expression driven by HbP2, and find that the prevailing model, based on pairwise cooperative binding of Bcd to HbP2 is not adequate. We demonstrate that other proteins, such as pioneer factors, Mediator and histone modifiers influence the shape and position of the HbP2 expression pattern. Comparing our results to theory reveals how higher-order cooperativity and energy expenditure impact boundary location and sharpness. Our results emphasize that the bacterial view of transcription regulation, where pairwise interactions between regulatory proteins dominate, must be reexamined in animals, where multiple molecular mechanisms collaborate to shape the gene regulatory function. |
format | Online Article Text |
id | pubmed-6588347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65883472019-06-24 Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity Park, Jeehae Estrada, Javier Johnson, Gemma Vincent, Ben J Ricci-Tam, Chiara Bragdon, Meghan DJ Shulgina, Yekaterina Cha, Anna Wunderlich, Zeba Gunawardena, Jeremy DePace, Angela H eLife Chromosomes and Gene Expression Developmental enhancers integrate graded concentrations of transcription factors (TFs) to create sharp gene expression boundaries. Here we examine the hunchback P2 (HbP2) enhancer which drives a sharp expression pattern in the Drosophila blastoderm embryo in response to the transcriptional activator Bicoid (Bcd). We systematically interrogate cis and trans factors that influence the shape and position of expression driven by HbP2, and find that the prevailing model, based on pairwise cooperative binding of Bcd to HbP2 is not adequate. We demonstrate that other proteins, such as pioneer factors, Mediator and histone modifiers influence the shape and position of the HbP2 expression pattern. Comparing our results to theory reveals how higher-order cooperativity and energy expenditure impact boundary location and sharpness. Our results emphasize that the bacterial view of transcription regulation, where pairwise interactions between regulatory proteins dominate, must be reexamined in animals, where multiple molecular mechanisms collaborate to shape the gene regulatory function. eLife Sciences Publications, Ltd 2019-06-21 /pmc/articles/PMC6588347/ /pubmed/31223115 http://dx.doi.org/10.7554/eLife.41266 Text en © 2019, Park et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Chromosomes and Gene Expression Park, Jeehae Estrada, Javier Johnson, Gemma Vincent, Ben J Ricci-Tam, Chiara Bragdon, Meghan DJ Shulgina, Yekaterina Cha, Anna Wunderlich, Zeba Gunawardena, Jeremy DePace, Angela H Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity |
title | Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity |
title_full | Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity |
title_fullStr | Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity |
title_full_unstemmed | Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity |
title_short | Dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity |
title_sort | dissecting the sharp response of a canonical developmental enhancer reveals multiple sources of cooperativity |
topic | Chromosomes and Gene Expression |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588347/ https://www.ncbi.nlm.nih.gov/pubmed/31223115 http://dx.doi.org/10.7554/eLife.41266 |
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