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A model of spatially restricted transcription in opposing gradients of activators and repressors
Morphogens control patterns of transcription in development, often by establishing concentration gradients of a single transcriptional activator. However, many morphogens, including Hedgehog, create opposing activator and repressor gradients (OARGs). In contrast to single activator gradients, it is...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Molecular Biology Organization
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472688/ https://www.ncbi.nlm.nih.gov/pubmed/23010997 http://dx.doi.org/10.1038/msb.2012.48 |
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author | White, Michael A Parker, Davis S Barolo, Scott Cohen, Barak A |
author_facet | White, Michael A Parker, Davis S Barolo, Scott Cohen, Barak A |
author_sort | White, Michael A |
collection | PubMed |
description | Morphogens control patterns of transcription in development, often by establishing concentration gradients of a single transcriptional activator. However, many morphogens, including Hedgehog, create opposing activator and repressor gradients (OARGs). In contrast to single activator gradients, it is not well understood how OARGs control transcriptional patterns. We present a general thermodynamic model that explains how spatial patterns of gene expression are established within OARGs. The model predicts that differences in enhancer binding site affinities for morphogen-responsive transcription factors (TFs) produce discrete transcriptional boundaries, but only when either activators or repressors bind cooperatively. This model quantitatively predicts the boundaries of gene expression within OARGs. When trained on experimental data, our model accounts for the counterintuitive observation that increasing the affinity of binding sites in enhancers of Hedgehog target genes produces more restricted transcription within Hedgehog gradients in Drosophila. Because our model is general, it may explain the role of low-affinity binding sites in many contexts, including mammalian Hedgehog gradients. |
format | Online Article Text |
id | pubmed-3472688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | European Molecular Biology Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-34726882012-10-16 A model of spatially restricted transcription in opposing gradients of activators and repressors White, Michael A Parker, Davis S Barolo, Scott Cohen, Barak A Mol Syst Biol Article Morphogens control patterns of transcription in development, often by establishing concentration gradients of a single transcriptional activator. However, many morphogens, including Hedgehog, create opposing activator and repressor gradients (OARGs). In contrast to single activator gradients, it is not well understood how OARGs control transcriptional patterns. We present a general thermodynamic model that explains how spatial patterns of gene expression are established within OARGs. The model predicts that differences in enhancer binding site affinities for morphogen-responsive transcription factors (TFs) produce discrete transcriptional boundaries, but only when either activators or repressors bind cooperatively. This model quantitatively predicts the boundaries of gene expression within OARGs. When trained on experimental data, our model accounts for the counterintuitive observation that increasing the affinity of binding sites in enhancers of Hedgehog target genes produces more restricted transcription within Hedgehog gradients in Drosophila. Because our model is general, it may explain the role of low-affinity binding sites in many contexts, including mammalian Hedgehog gradients. European Molecular Biology Organization 2012-09-25 /pmc/articles/PMC3472688/ /pubmed/23010997 http://dx.doi.org/10.1038/msb.2012.48 Text en Copyright © 2012, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial Share Alike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission. |
spellingShingle | Article White, Michael A Parker, Davis S Barolo, Scott Cohen, Barak A A model of spatially restricted transcription in opposing gradients of activators and repressors |
title | A model of spatially restricted transcription in opposing gradients of activators and repressors |
title_full | A model of spatially restricted transcription in opposing gradients of activators and repressors |
title_fullStr | A model of spatially restricted transcription in opposing gradients of activators and repressors |
title_full_unstemmed | A model of spatially restricted transcription in opposing gradients of activators and repressors |
title_short | A model of spatially restricted transcription in opposing gradients of activators and repressors |
title_sort | model of spatially restricted transcription in opposing gradients of activators and repressors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472688/ https://www.ncbi.nlm.nih.gov/pubmed/23010997 http://dx.doi.org/10.1038/msb.2012.48 |
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