@article {cite-key,
	title = {Isolation and characterization of a mouse homolog of the Drosophila segment polarity gene dishevelled.},
	journal = {Dev Biol},
	volume = {166},
	number = {1},
	year = {1994},
	month = {Nov},
	pages = {73{\textendash}86},
	address = {Department of Obstetrics and Gynecology, University of Maryland School of Medicine, Baltimore 21201-1559.},
	abstract = {In the Drosophila embryo dishevelled (dsh) function is required by target cells in order to respond to wingless (wg, the homolog of Wnt-1), demonstrating a role for dsh in Wnt signal transduction. We have isolated a mouse homolog of the Drosophila dsh segment polarity gene. The 695-amino-acid protein encoded by the mouse dishevelled gene (Dvl-1) shares 50\% identity (65\% similarity) with dsh. Similarity searches of protein and DNA data bases revealed that Dvl-1 encodes an otherwise novel polypeptide. While no functional motifs were identified, one region of Dvl-1 was found to be similar to a domain of discs large-1 (dlg), a Drosophila tumor suppressor gene. In the embryo, Dvl-1 is expressed in most tissues, with uniformly high levels in the central nervous system. From 7.5 days postcoitum Dvl-1 is expressed throughout the developing brain and spinal cord, including those regions expressing Wnt-1 and En. Expression of Dvl-1 in adult mice was found to be widespread, with brain and testis exhibiting the highest levels. The majority of Dvl-1 expression in the adult cerebellum is in the granular cell layer, similar to the pattern seen for engrailed-2 (En-2). Throughout postnatal development of the brain Dvl-1 is highly expressed in areas of high neuronal cell density.},
	issn = {0012-1606 (Print); 0012-1606 (Linking)},
	doi = {10.1006/dbio.1994.1297},
	author = {Sussman, D J and Klingensmith, J and Salinas, P and Adams, P S and Nusse, R and Perrimon, N}
}
