Integration of growth and specification in chick wing digit-patterning

An additional function for Sonic hedgehog (Shh) in the limb bud is identified, namely the control of expression of cell cycle regulators, thereby controlling growth and specifying the size of the field in which the digit specification gradient operates. It is found that when Shh signalling was inhib...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature 2008-04, Vol.452 (7189), p.882-886
Hauptverfasser: Towers, Matthew, Mahood, Ruth, Yin, Yili, Tickle, Cheryll
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:An additional function for Sonic hedgehog (Shh) in the limb bud is identified, namely the control of expression of cell cycle regulators, thereby controlling growth and specifying the size of the field in which the digit specification gradient operates. It is found that when Shh signalling was inhibited in chick limb buds, all the digit precursors formed anterior structures. In contrast, when cell proliferation was inhibited, all the anterior structures were lost and all the digit-precursors formed posterior structures. In the classical model of chick wing digit-patterning 1 , the polarizing region—a group of cells at the posterior margin of the early bud—produces a morphogen gradient, now known to be based on Sonic hedgehog (Shh) 2 , 3 , that progressively specifies anteroposterior positional identities in the posterior digit-forming region 4 . Here we add an integral growth component to this model by showing that Shh-dependent proliferation of prospective digit progenitor cells is essential for specifying the complete pattern of digits across the anteroposterior axis. Inhibiting Shh signalling in early wing buds reduced anteroposterior expansion, and posterior digits were lost because all prospective digit precursors formed anterior structures. Inhibiting proliferation also irreversibly reduced anteroposterior expansion, but instead anterior digits were lost because all prospective digit precursors formed posterior structures. When proliferation recovered in such wings, Shh transcription was maintained for longer than normal, suggesting that duration of Shh expression is controlled by a mechanism that measures proliferation. Rescue experiments confirmed that Shh-dependent proliferation controls digit number during a discrete time-window in which Shh-dependent specification normally occurs. Our findings that Shh signalling has dual functions that can be temporally uncoupled have implications for understanding congenital and evolutionary digit reductions.
ISSN:0028-0836
1476-4687
1476-4679
DOI:10.1038/nature06718