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   <subfield code="a">WNT-mediated relocalization of dishevelled proteins</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Susan Steitz, Michael Tsang, Daniel Sussman]</subfield>
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   <subfield code="a">Summary: TheWnt family of proto-oncogenes encodes secreted signaling proteins that are required for mouse development. TheDrosophila Wnt homolog, thewingless (Wg) segment polarity gene, mediates a signal transduction pathway in which the downstream elements appear to be conserved through evolution. One such element, thedishevelled gene product, becomes hyperphosphorylated and translocates to the plasma membrane in response to Wg (Yanagawa et al., 1995). We report here that the mouseDishevelle-1 (Dvl-1) andDishevelled-2 genes encode proteins that are differentially localized inWnt-overexpressing PC12 cell lines (PC12/Wnt). WhereasDvl-1 andDvl-2 proteins are limited to the soluble fraction of parental PC12 cells, PC12/Wnt cells display a subset ofDvl-1 protein associated with the membrane andDvl-2 protein with the cytoskeletal fraction. These results suggest a conserved role forDvl inWnt/wg signal transduction.</subfield>
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   <subfield code="u">Department of Obstetrics and Gynecology, Division of Human Genetics, University of Maryland School of Medicine, 655 West Baltimore Street, 21201, Baltimore, Maryland</subfield>
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   <subfield code="u">Department of Obstetrics and Gynecology, Division of Human Genetics, University of Maryland School of Medicine, 655 West Baltimore Street, 21201, Baltimore, Maryland</subfield>
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   <subfield code="t">In Vitro Cellular &amp; Developmental Biology - Animal</subfield>
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   <subfield code="g">32/7(1996-07-01), 441-445</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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