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Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity
Precise cis-regulatory control of gene expression is essential for normal embryogenesis and tissue development. The BMP antagonist Gremlin1 (Grem1) is a key node in the signalling system that coordinately controls limb bud development. Here, we use mouse reverse genetics to identify the enhancers in...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455560/ https://www.ncbi.nlm.nih.gov/pubmed/34548488 http://dx.doi.org/10.1038/s41467-021-25810-1 |
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author | Malkmus, Jonas Ramos Martins, Laurène Jhanwar, Shalu Kircher, Bonnie Palacio, Victorio Sheth, Rushikesh Leal, Francisca Duchesne, Amandine Lopez-Rios, Javier Peterson, Kevin A. Reinhardt, Robert Onimaru, Koh Cohn, Martin J. Zuniga, Aimée Zeller, Rolf |
author_facet | Malkmus, Jonas Ramos Martins, Laurène Jhanwar, Shalu Kircher, Bonnie Palacio, Victorio Sheth, Rushikesh Leal, Francisca Duchesne, Amandine Lopez-Rios, Javier Peterson, Kevin A. Reinhardt, Robert Onimaru, Koh Cohn, Martin J. Zuniga, Aimée Zeller, Rolf |
author_sort | Malkmus, Jonas |
collection | PubMed |
description | Precise cis-regulatory control of gene expression is essential for normal embryogenesis and tissue development. The BMP antagonist Gremlin1 (Grem1) is a key node in the signalling system that coordinately controls limb bud development. Here, we use mouse reverse genetics to identify the enhancers in the Grem1 genomic landscape and the underlying cis-regulatory logics that orchestrate the spatio-temporal Grem1 expression dynamics during limb bud development. We establish that transcript levels are controlled in an additive manner while spatial regulation requires synergistic interactions among multiple enhancers. Disrupting these interactions shows that altered spatial regulation rather than reduced Grem1 transcript levels prefigures digit fusions and loss. Two of the enhancers are evolutionary ancient and highly conserved from basal fishes to mammals. Analysing these enhancers from different species reveal the substantial spatial plasticity in Grem1 regulation in tetrapods and basal fishes, which provides insights into the fin-to-limb transition and evolutionary diversification of pentadactyl limbs. |
format | Online Article Text |
id | pubmed-8455560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84555602021-10-07 Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity Malkmus, Jonas Ramos Martins, Laurène Jhanwar, Shalu Kircher, Bonnie Palacio, Victorio Sheth, Rushikesh Leal, Francisca Duchesne, Amandine Lopez-Rios, Javier Peterson, Kevin A. Reinhardt, Robert Onimaru, Koh Cohn, Martin J. Zuniga, Aimée Zeller, Rolf Nat Commun Article Precise cis-regulatory control of gene expression is essential for normal embryogenesis and tissue development. The BMP antagonist Gremlin1 (Grem1) is a key node in the signalling system that coordinately controls limb bud development. Here, we use mouse reverse genetics to identify the enhancers in the Grem1 genomic landscape and the underlying cis-regulatory logics that orchestrate the spatio-temporal Grem1 expression dynamics during limb bud development. We establish that transcript levels are controlled in an additive manner while spatial regulation requires synergistic interactions among multiple enhancers. Disrupting these interactions shows that altered spatial regulation rather than reduced Grem1 transcript levels prefigures digit fusions and loss. Two of the enhancers are evolutionary ancient and highly conserved from basal fishes to mammals. Analysing these enhancers from different species reveal the substantial spatial plasticity in Grem1 regulation in tetrapods and basal fishes, which provides insights into the fin-to-limb transition and evolutionary diversification of pentadactyl limbs. Nature Publishing Group UK 2021-09-21 /pmc/articles/PMC8455560/ /pubmed/34548488 http://dx.doi.org/10.1038/s41467-021-25810-1 Text en © The Author(s) 2021 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 Malkmus, Jonas Ramos Martins, Laurène Jhanwar, Shalu Kircher, Bonnie Palacio, Victorio Sheth, Rushikesh Leal, Francisca Duchesne, Amandine Lopez-Rios, Javier Peterson, Kevin A. Reinhardt, Robert Onimaru, Koh Cohn, Martin J. Zuniga, Aimée Zeller, Rolf Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity |
title | Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity |
title_full | Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity |
title_fullStr | Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity |
title_full_unstemmed | Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity |
title_short | Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity |
title_sort | spatial regulation by multiple gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455560/ https://www.ncbi.nlm.nih.gov/pubmed/34548488 http://dx.doi.org/10.1038/s41467-021-25810-1 |
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