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An ancient yet flexible cis-regulatory architecture allows localized Hedgehog tuning by patched/Ptch1
The Hedgehog signaling pathway is part of the ancient developmental-evolutionary animal toolkit. Frequently co-opted to pattern new structures, the pathway is conserved among eumetazoans yet flexible and pleiotropic in its effects. The Hedgehog receptor, Patched, is transcriptionally activated by He...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887206/ https://www.ncbi.nlm.nih.gov/pubmed/27146892 http://dx.doi.org/10.7554/eLife.13550 |
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author | Lorberbaum, David S Ramos, Andrea I Peterson, Kevin A Carpenter, Brandon S Parker, David S De, Sandip Hillers, Lauren E Blake, Victoria M Nishi, Yuichi McFarlane, Matthew R Chiang, Ason CY Kassis, Judith A Allen, Benjamin L McMahon, Andrew P Barolo, Scott |
author_facet | Lorberbaum, David S Ramos, Andrea I Peterson, Kevin A Carpenter, Brandon S Parker, David S De, Sandip Hillers, Lauren E Blake, Victoria M Nishi, Yuichi McFarlane, Matthew R Chiang, Ason CY Kassis, Judith A Allen, Benjamin L McMahon, Andrew P Barolo, Scott |
author_sort | Lorberbaum, David S |
collection | PubMed |
description | The Hedgehog signaling pathway is part of the ancient developmental-evolutionary animal toolkit. Frequently co-opted to pattern new structures, the pathway is conserved among eumetazoans yet flexible and pleiotropic in its effects. The Hedgehog receptor, Patched, is transcriptionally activated by Hedgehog, providing essential negative feedback in all tissues. Our locus-wide dissections of the cis-regulatory landscapes of fly patched and mouse Ptch1 reveal abundant, diverse enhancers with stage- and tissue-specific expression patterns. The seemingly simple, constitutive Hedgehog response of patched/Ptch1 is driven by a complex regulatory architecture, with batteries of context-specific enhancers engaged in promoter-specific interactions to tune signaling individually in each tissue, without disturbing patterning elsewhere. This structure—one of the oldest cis-regulatory features discovered in animal genomes—explains how patched/Ptch1 can drive dramatic adaptations in animal morphology while maintaining its essential core function. It may also suggest a general model for the evolutionary flexibility of conserved regulators and pathways. DOI: http://dx.doi.org/10.7554/eLife.13550.001 |
format | Online Article Text |
id | pubmed-4887206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48872062016-06-02 An ancient yet flexible cis-regulatory architecture allows localized Hedgehog tuning by patched/Ptch1 Lorberbaum, David S Ramos, Andrea I Peterson, Kevin A Carpenter, Brandon S Parker, David S De, Sandip Hillers, Lauren E Blake, Victoria M Nishi, Yuichi McFarlane, Matthew R Chiang, Ason CY Kassis, Judith A Allen, Benjamin L McMahon, Andrew P Barolo, Scott eLife Developmental Biology and Stem Cells The Hedgehog signaling pathway is part of the ancient developmental-evolutionary animal toolkit. Frequently co-opted to pattern new structures, the pathway is conserved among eumetazoans yet flexible and pleiotropic in its effects. The Hedgehog receptor, Patched, is transcriptionally activated by Hedgehog, providing essential negative feedback in all tissues. Our locus-wide dissections of the cis-regulatory landscapes of fly patched and mouse Ptch1 reveal abundant, diverse enhancers with stage- and tissue-specific expression patterns. The seemingly simple, constitutive Hedgehog response of patched/Ptch1 is driven by a complex regulatory architecture, with batteries of context-specific enhancers engaged in promoter-specific interactions to tune signaling individually in each tissue, without disturbing patterning elsewhere. This structure—one of the oldest cis-regulatory features discovered in animal genomes—explains how patched/Ptch1 can drive dramatic adaptations in animal morphology while maintaining its essential core function. It may also suggest a general model for the evolutionary flexibility of conserved regulators and pathways. DOI: http://dx.doi.org/10.7554/eLife.13550.001 eLife Sciences Publications, Ltd 2016-05-05 /pmc/articles/PMC4887206/ /pubmed/27146892 http://dx.doi.org/10.7554/eLife.13550 Text en http://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Developmental Biology and Stem Cells Lorberbaum, David S Ramos, Andrea I Peterson, Kevin A Carpenter, Brandon S Parker, David S De, Sandip Hillers, Lauren E Blake, Victoria M Nishi, Yuichi McFarlane, Matthew R Chiang, Ason CY Kassis, Judith A Allen, Benjamin L McMahon, Andrew P Barolo, Scott An ancient yet flexible cis-regulatory architecture allows localized Hedgehog tuning by patched/Ptch1 |
title | An ancient yet flexible cis-regulatory architecture allows localized Hedgehog tuning by patched/Ptch1 |
title_full | An ancient yet flexible cis-regulatory architecture allows localized Hedgehog tuning by patched/Ptch1 |
title_fullStr | An ancient yet flexible cis-regulatory architecture allows localized Hedgehog tuning by patched/Ptch1 |
title_full_unstemmed | An ancient yet flexible cis-regulatory architecture allows localized Hedgehog tuning by patched/Ptch1 |
title_short | An ancient yet flexible cis-regulatory architecture allows localized Hedgehog tuning by patched/Ptch1 |
title_sort | ancient yet flexible cis-regulatory architecture allows localized hedgehog tuning by patched/ptch1 |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4887206/ https://www.ncbi.nlm.nih.gov/pubmed/27146892 http://dx.doi.org/10.7554/eLife.13550 |
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