Satb2, modularity, and the evolvability of the vertebrate jaw
Article first published online: 21 NOV 2011
© 2011 Wiley Periodicals, Inc.
Evolution & Development
Volume 13, Issue 6, pages 549–564, November/December 2011
How to Cite
Fish, J. L., Villmoare, B., Köbernick, K., Compagnucci, C., Britanova, O., Tarabykin, V. and Depew, M. J. (2011), Satb2, modularity, and the evolvability of the vertebrate jaw. Evolution & Development, 13: 549–564. doi: 10.1111/j.1525-142X.2011.00511.x
- Issue published online: 21 NOV 2011
- Article first published online: 21 NOV 2011
- HFSP. Grant Number: LT 01061/2007-L
- Marie Curie Early Training Fellowship. Grant Number: MEST-CT-2004-504025
- Royal Society, the Dental Institute of King's College London
- Friends of Guy's Hospital
Modularity is a key mechanism bridging development and evolution and is fundamental to evolvability. Herein, we investigate modularity of the Vertebrate jaw with the aim of understanding mechanisms of its morphological evolution. Conservation of the basic structural bauplan of Vertebrate jaws led to a Hinge and Caps model, in which polarity in the patterning system of developing jaws predicts modularity. We have tested the hypothesis that the Satb2+ cell population delineates a developmental module within the mandibular jaw. Satb2 is expressed in the mesenchyme of the jaw primordia that gives rise to distal elements of both the upper and lower jaws. Loss of Satb2 specifically affects structural elements of the distal (incisor) domain, reflecting the integration of these elements as well as their independence from other mandibular domains. Reducing Satb2 dosage leads to an increase in variation in mandibular length, providing insight into the developmental potential to generate variation. Inter-taxa comparisons reveal that the Satb2 domain is conserved within gnathostomes. We complement previous loss of function studies in mice with gene knock-down experiments in Xenopus, providing evidence for functional conservation of Satb2 in regulating size. Finally, we present evidence that the relative size of the amniote mandibular Satb2+ domain varies in relation to epithelial Fgf8 expression, suggesting a mechanism for evolutionary change in this domain. Taken together, our data support the Hinge and Caps model and provide evidence that Satb2 regulates coordinated distal jaw modules that are subject to evolutionary modification by signals emanating from the Hinge.