%0 Journal Article %J Dev Biol %D 1994 %T Isolation and characterization of a mouse homolog of the Drosophila segment polarity gene dishevelled. %A Sussman, D J %A Klingensmith, J %A Salinas, P %A Adams, P S %A Nusse, R %A Perrimon, N %K Adaptor Proteins, Signal Transducing %K Aging %K Amino Acid Sequence %K Animals %K Base Sequence %K Brain %K DNA %K DNA Primers %K Drosophila %K Embryo, Nonmammalian %K Embryonic and Fetal Development %K Gene Expression %K Gestational Age %K Humans %K Male %K Mice %K Molecular Sequence Data %K Organ Specificity %K Phosphoproteins %K Polymerase Chain Reaction %K Protein Biosynthesis %K Proteins %K Restriction Mapping %K RNA, Messenger %K Sequence Homology, Amino Acid %K Species Specificity %K Spinal Cord %K Testis %X

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.

%B Dev Biol %V 166 %P 73-86 %8 1994 Nov %G eng %N 1 %1 http://www.ncbi.nlm.nih.gov/pubmed/7958461?dopt=Abstract %R 10.1006/dbio.1994.1297