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GLI transcriptional repression is inert prior to Hedgehog pathway activation
The Hedgehog (HH) pathway regulates a spectrum of developmental processes through the transcriptional mediation of GLI proteins. GLI repressors control tissue patterning by preventing sub-threshold activation of HH target genes, presumably even before HH induction, while lack of GLI repression activ...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831537/ https://www.ncbi.nlm.nih.gov/pubmed/35145123 http://dx.doi.org/10.1038/s41467-022-28485-4 |
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author | Lex, Rachel K. Zhou, Weiqiang Ji, Zhicheng Falkenstein, Kristin N. Schuler, Kaleigh E. Windsor, Kathryn E. Kim, Joseph D. Ji, Hongkai Vokes, Steven A. |
author_facet | Lex, Rachel K. Zhou, Weiqiang Ji, Zhicheng Falkenstein, Kristin N. Schuler, Kaleigh E. Windsor, Kathryn E. Kim, Joseph D. Ji, Hongkai Vokes, Steven A. |
author_sort | Lex, Rachel K. |
collection | PubMed |
description | The Hedgehog (HH) pathway regulates a spectrum of developmental processes through the transcriptional mediation of GLI proteins. GLI repressors control tissue patterning by preventing sub-threshold activation of HH target genes, presumably even before HH induction, while lack of GLI repression activates most targets. Despite GLI repression being central to HH regulation, it is unknown when it first becomes established in HH-responsive tissues. Here, we investigate whether GLI3 prevents precocious gene expression during limb development. Contrary to current dogma, we find that GLI3 is inert prior to HH signaling. While GLI3 binds to most targets, loss of Gli3 does not increase target gene expression, enhancer acetylation or accessibility, as it does post-HH signaling. Furthermore, GLI repression is established independently of HH signaling, but after its onset. Collectively, these surprising results challenge current GLI pre-patterning models and demonstrate that GLI repression is not a default state for the HH pathway. |
format | Online Article Text |
id | pubmed-8831537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88315372022-03-04 GLI transcriptional repression is inert prior to Hedgehog pathway activation Lex, Rachel K. Zhou, Weiqiang Ji, Zhicheng Falkenstein, Kristin N. Schuler, Kaleigh E. Windsor, Kathryn E. Kim, Joseph D. Ji, Hongkai Vokes, Steven A. Nat Commun Article The Hedgehog (HH) pathway regulates a spectrum of developmental processes through the transcriptional mediation of GLI proteins. GLI repressors control tissue patterning by preventing sub-threshold activation of HH target genes, presumably even before HH induction, while lack of GLI repression activates most targets. Despite GLI repression being central to HH regulation, it is unknown when it first becomes established in HH-responsive tissues. Here, we investigate whether GLI3 prevents precocious gene expression during limb development. Contrary to current dogma, we find that GLI3 is inert prior to HH signaling. While GLI3 binds to most targets, loss of Gli3 does not increase target gene expression, enhancer acetylation or accessibility, as it does post-HH signaling. Furthermore, GLI repression is established independently of HH signaling, but after its onset. Collectively, these surprising results challenge current GLI pre-patterning models and demonstrate that GLI repression is not a default state for the HH pathway. Nature Publishing Group UK 2022-02-10 /pmc/articles/PMC8831537/ /pubmed/35145123 http://dx.doi.org/10.1038/s41467-022-28485-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lex, Rachel K. Zhou, Weiqiang Ji, Zhicheng Falkenstein, Kristin N. Schuler, Kaleigh E. Windsor, Kathryn E. Kim, Joseph D. Ji, Hongkai Vokes, Steven A. GLI transcriptional repression is inert prior to Hedgehog pathway activation |
title | GLI transcriptional repression is inert prior to Hedgehog pathway activation |
title_full | GLI transcriptional repression is inert prior to Hedgehog pathway activation |
title_fullStr | GLI transcriptional repression is inert prior to Hedgehog pathway activation |
title_full_unstemmed | GLI transcriptional repression is inert prior to Hedgehog pathway activation |
title_short | GLI transcriptional repression is inert prior to Hedgehog pathway activation |
title_sort | gli transcriptional repression is inert prior to hedgehog pathway activation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831537/ https://www.ncbi.nlm.nih.gov/pubmed/35145123 http://dx.doi.org/10.1038/s41467-022-28485-4 |
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