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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
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.
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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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