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Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity

Author

Listed:
  • Jonas Malkmus

    (University of Basel)

  • Laurène Ramos Martins

    (University of Basel)

  • Shalu Jhanwar

    (University of Basel
    University of Basel)

  • Bonnie Kircher

    (University of Florida)

  • Victorio Palacio

    (University of Basel)

  • Rushikesh Sheth

    (University of Basel)

  • Francisca Leal

    (University of Florida)

  • Amandine Duchesne

    (Université Paris-Saclay, INRAE, AgroParisTech, GABI)

  • Javier Lopez-Rios

    (CSIC-Universidad Pablo de Olavide-Junta de Andalucía)

  • Kevin A. Peterson

    (The Jackson Laboratory)

  • Robert Reinhardt

    (University of Basel)

  • Koh Onimaru

    (Laboratory for Bioinformatics Research, RIKEN BDR)

  • Martin J. Cohn

    (University of Florida
    University of Florida)

  • Aimée Zuniga

    (University of Basel)

  • Rolf Zeller

    (University of Basel)

Abstract

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.

Suggested Citation

  • Jonas Malkmus & Laurène Ramos Martins & Shalu Jhanwar & Bonnie Kircher & Victorio Palacio & Rushikesh Sheth & Francisca Leal & Amandine Duchesne & Javier Lopez-Rios & Kevin A. Peterson & Robert Reinha, 2021. "Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity," Nature Communications, Nature, vol. 12(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25810-1
    DOI: 10.1038/s41467-021-25810-1
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    Cited by:

    1. Anastasiia Lozovska & Artemis G. Korovesi & André Dias & Alexandre Lopes & Donald A. Fowler & Gabriel G. Martins & Ana Nóvoa & Moisés Mallo, 2024. "Tgfbr1 controls developmental plasticity between the hindlimb and external genitalia by remodeling their regulatory landscape," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    2. Marta Losa & Iros Barozzi & Marco Osterwalder & Viviana Hermosilla-Aguayo & Angela Morabito & Brandon H. Chacón & Peyman Zarrineh & Ausra Girdziusaite & Jean Denis Benazet & Jianjian Zhu & Susan Macke, 2023. "A spatio-temporally constrained gene regulatory network directed by PBX1/2 acquires limb patterning specificity via HAND2," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
    3. Raquel Rouco & Olimpia Bompadre & Antonella Rauseo & Olivier Fazio & Rodrigue Peraldi & Fabrizio Thorel & Guillaume Andrey, 2021. "Cell-specific alterations in Pitx1 regulatory landscape activation caused by the loss of a single enhancer," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
    4. Rachel K. Lex & Weiqiang Zhou & Zhicheng Ji & Kristin N. Falkenstein & Kaleigh E. Schuler & Kathryn E. Windsor & Joseph D. Kim & Hongkai Ji & Steven A. Vokes, 2022. "GLI transcriptional repression is inert prior to Hedgehog pathway activation," Nature Communications, Nature, vol. 13(1), pages 1-15, December.

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