Abstract

Turing models have been proposed to explain the emergence of digits during limb development. However, so far the molecular components that would give rise to Turing patterns are elusive. We have recently shown that a particular type of receptor-ligand interaction can give rise to Schnakenberg-type Turing patterns, which reproduce patterning during lung and kidney branching morphogenesis. Recent knockout experiments have identified Smad4 as a key protein in digit patterning. We show here that the BMP-receptor interaction meets the conditions for a Schnakenberg-type Turing pattern and that the resulting model reproduces available wildtype and mutant data on the expression patterns of BMP, its receptor and Fgfs in the apical ectodermal ridge (AER) when solved on a realistic 2D domain that we extracted from limb bud images of E11.5 mouse embryos. We propose that receptor-ligand-based mechanisms serve as a molecular basis for the emergence of Turing patterns in many developing tissues.

Project information

  • Category: Mathematical Modelling
  • Location: ETH Zurich
  • Project timeline: 2011-2012
  • Publication: Link

Figure legends and References

Figure 1: An advanced version of turing patterning with mechanical and biochemical elements

Figure 2: Big picture of the Regulatory network in the limb

Figure 3: Simulated regulatory network in the limb

Figure 4: Results. Adapted from Link

Reference Manuscript: Link

Reference Masters Thesis: Link