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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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.
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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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