Fgf signalling triggers an intrinsic mesodermal timer that determines the duration of limb patterning.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
20 09 2023
Historique:
received: 22 02 2023
accepted: 05 09 2023
medline: 22 9 2023
pubmed: 21 9 2023
entrez: 20 9 2023
Statut: epublish

Résumé

Complex signalling between the apical ectodermal ridge (AER - a thickening of the distal epithelium) and the mesoderm controls limb patterning along the proximo-distal axis (humerus to digits). However, the essential in vivo requirement for AER-Fgf signalling makes it difficult to understand the exact roles that it fulfils. To overcome this barrier, we developed an amenable ex vivo chick wing tissue explant system that faithfully replicates in vivo parameters. Using inhibition experiments and RNA-sequencing, we identify a transient role for Fgfs in triggering the distal patterning phase. Fgfs are then dispensable for the maintenance of an intrinsic mesodermal transcriptome, which controls proliferation/differentiation timing and the duration of patterning. We also uncover additional roles for Fgf signalling in maintaining AER-related gene expression and in suppressing myogenesis. We describe a simple logic for limb patterning duration, which is potentially applicable to other systems, including the main body axis.

Identifiants

pubmed: 37730682
doi: 10.1038/s41467-023-41457-6
pii: 10.1038/s41467-023-41457-6
pmc: PMC10511490
doi:

Substances chimiques

Fibroblast Growth Factors 62031-54-3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5841

Subventions

Organisme : Wellcome Trust
ID : 202756/Z/16/Z
Pays : United Kingdom

Informations de copyright

© 2023. Springer Nature Limited.

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Auteurs

Sofia Sedas Perez (S)

School of Biosciences, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.

Caitlin McQueen (C)

School of Biosciences, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.
Chester Medical School, Chester, CH2 1BR, UK.

Holly Stainton (H)

School of Biosciences, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.

Joseph Pickering (J)

School of Biosciences, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.

Kavitha Chinnaiya (K)

School of Biosciences, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.

Patricia Saiz-Lopez (P)

Instituto de Biomedicina y Biotecnología de Cantabria, IBBTEC (CSIC-Universidad de Cantabria), 39011, Santander, Spain.
Departamento de Anatomía y Biología Celular Facultad de Medicina, Universidad de Cantabria, 39011, Santander, Spain.

Marysia Placzek (M)

School of Biosciences, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.

Maria A Ros (MA)

Instituto de Biomedicina y Biotecnología de Cantabria, IBBTEC (CSIC-Universidad de Cantabria), 39011, Santander, Spain.
Departamento de Anatomía y Biología Celular Facultad de Medicina, Universidad de Cantabria, 39011, Santander, Spain.

Matthew Towers (M)

School of Biosciences, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK. m.towers@sheffield.ac.uk.

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Classifications MeSH