Spatial regulation by multiple Gremlin1 enhancers provides digit development with cis-regulatory robustness and evolutionary plasticity
Jonas Malkmus,
Laurène Ramos Martins,
Shalu Jhanwar,
Bonnie Kircher,
Victorio Palacio,
Rushikesh Sheth,
Francisca Leal,
Amandine Duchesne,
Javier Lopez-Rios,
Kevin A. Peterson,
Robert Reinhardt,
Koh Onimaru,
Martin J. Cohn,
Aimée Zuniga () and
Rolf Zeller ()
Additional contact information
Jonas Malkmus: University of Basel
Laurène Ramos Martins: University of Basel
Shalu Jhanwar: 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
Aimée Zuniga: University of Basel
Rolf Zeller: University of Basel
Nature Communications, 2021, vol. 12, issue 1, 1-17
Abstract:
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.
Date: 2021
References: Add references at CitEc
Citations: View citations in EconPapers (5)
Downloads: (external link)
https://www.nature.com/articles/s41467-021-25810-1 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25810-1
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-021-25810-1
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().