Joint interpretation of AER/FGF and ZPA/SHH over time and space underlies hairy...

• Autor(es): Sheeba, Caroline J. ; Palmeirim, I. ; Andrade, Raquel P.
• Data: 2012
• Identificador Persistente: http://hdl.handle.net/1822/21013
• Origem: RepositóriUM - Universidade do Minho
• Assunto(s): Fibroblast growth factor; HES expression; Limb development; Sonic hedgehog
• Tipo de Documento: Artigo
• Idioma: Inglês

Descrição

The authors are grateful to Cheryll Tickle and Lewis Wolpert for helpful comments and critical reading of the manuscript, to Lisa Gonc¸alves and Tatiana Resende for fruitful discussions, Rute Moura and Paulina Piairo for technical assistance and Baolin Wang for the kind gift of Gli3 antibody. Embryo development requires precise orchestration of cell proliferation and differentiation in both time and space. A molecular clock operating through gene expression oscillations was first described in the presomitic mesoderm (PSM) underlying periodic somite formation. Cycles of HES gene expression have been further identified in other progenitor cells, including the chick distal limb mesenchyme, embryonic neural progenitors and both mesenchymal and embryonic stem cells. In the limb, hairy2 is expressed in the distal mesenchyme, adjacent to the FGF source (AER) and along the ZPA-derived SHH gradient, the two major regulators of limb development. Here we report that hairy2 expression depends on joint AER/FGF and ZPA/SHH signaling. FGF plays an instructive role on hairy2, mediated by Erk and Akt pathway activation, while SHH acts by creating a permissive state defined by Gli3-A/Gli3-R.1. Moreover, we show that AER/FGF and ZPA/SHH present distinct temporal and spatial signaling properties in the distal limb mesenchyme: SHH acts at a long-term, long-range on hairy2, while FGF has a shortterm, short-range action. Our work establishes limb hairy2 expression as an output of integrated FGF and SHH signaling in time and space, providing novel clues for understanding the regulatory mechanisms underlying HES oscillations in multiple systems, including embryonic stem cell pluripotency.