Mouse Disp1 is required in sonic hedgehog-expressing cells for paracrine activity of the cholesterol-modified ligand

Abstract

We have repeated the facial analysis reported in Fig. 2 to provide the data required to support some of the original findings of this study (see Publisher's note). Our findings substantiate the original conclusions drawn from Fig. 2 of a dose-related genetic interaction between Disp1 and Shh alleles, and of the function of Disp1 within Shh-producing cells. Some differences are reported below, which might reflect slight differences in embryonic staging or increased sensitivity of the whole-mount in situ hybridization procedure here. Importantly, they do not alter the key conclusion that reducing Disp1 levels in Shh-producing cells results in a phenotype similar to that of genetically matched embryos with reduced Disp1 activity throughout the embryo. These data support the overall conclusions of the paper, and, together with other data in the same report, support a model in which the principal requirement for Disp1 activity is in Shh-producing cells.