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In vertebrates, cranial placodes contribute to all sense organs and sensory ganglia and arise from a common pool of Six1/Eya2+ progenitors. Here we dissect the events that specify ectodermal cells as placode progenitors using newly identified genes upstream of the Six/Eya complex. We show in chick that two different tissues, namely the lateral head mesoderm and the prechordal mesendoderm, gradually induce placode progenitors: cells pass through successive transcriptional states, each identified by distinct factors and controlled by different signals. Both tissues initiate a common transcriptional state but over time impart regional character, with the acquisition of anterior identity dependent on Shh signalling. Using a network inference approach we predict the regulatory relationships among newly identified transcription factors and verify predicted links in knockdown experiments. Based on this analysis we propose a new model for placode progenitor induction, in which the initial induction of a generic transcriptional state precedes regional divergence.
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http://dx.doi.org/10.1242/dev.147942 | DOI Listing |
Development
April 2025
Centre for Craniofacial and Regenerative Biology, King's College London, London SE1 9RT, UK.
Branchio-otic (BOS) and branchio-oto-renal (BOR) syndromes are autosomal dominant disorders featuring multiple birth defects including ear, renal and branchial malformations. Mutations in the homeodomain transcription factor SIX1 and its co-factor EYA1 have been identified in about 50% of individuals with BOS or BOR, while causative mutations are unknown in the other half. We hypothesise that SIX1 target genes represent new BOS and BOR candidates.
View Article and Find Full Text PDFDev Biol
July 2025
Centre for Craniofacial and Regenerative Biology, King's College London, UK. Electronic address:
The neural plate border is transient territory surrounding the anterior neural plate containing precursors for all ectodermal derivatives: the neural plate, neural crest cells, sensory placodes and the epidermis. A long-standing question is whether its resident cells are already biased to their future identity, whether they represent multipotent progenitor cells and if so, how these lineages segregate. Here, I review the studies that originally defined the neural plate border including lineage tracing, gene expression and functional data.
View Article and Find Full Text PDFScience
April 2025
Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
Placodes and the neural crest are defining features of vertebrates. In this study, we investigate their lineages in mice using in utero approaches. We demonstrated that nanoinjection at embryonic day 7.
View Article and Find Full Text PDFGene Expr Patterns
June 2025
Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX, 75390, USA. Electronic address:
All pancreatic lineages originate from a transitory structure known as the multipotent progenitor epithelium (MPE), which is an endodermal placode formed via epithelial stratification. Cells within the MPE undergo de novo lumenogenesis to give rise to an epithelial plexus, which serves as a progenitor niche for subsequent development of endocrine, ductal and acinar cell types. Recent evidence suggests that Hippo signaling is required for pancreatic cell differentiation, but little is known about the function of Hippo signaling in the development of the MPE.
View Article and Find Full Text PDFElife
December 2024
Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, United States.
Two major ligand-receptor signaling axes - endothelin Edn3 and its receptor Ednrb, and glial-derived neurotrophic factor (GDNF) and its receptor Ret - are required for migration of enteric nervous system (ENS) progenitors to the hindgut. Mutations in either component cause colonic aganglionosis, also called Hirschsprung disease. Here, we have used Wnt1Cre and Pax2Cre in mice to show that these driver lines label distinct ENS lineages during progenitor migration and in their terminal hindgut fates.
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