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PMID: 8626800 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A large family of putative transmembrane receptors homologous to the product of the Drosophila tissue polarity gene frizzled.

The Journal of biological chemistry ·Vol. 271 ·No. 8 ·1996-02-23 ·Pages 4468-76

Wang Y, Macke JP, Abella BS, Andreasson K, Worley P, Gilbert DJ, Copeland NG, Jenkins NA, Nathans J

Abstract

In Drosophila melanogaster, the frizzled gene plays an essential role in the development of tissue polarity as assessed by the orientation of cuticular structures. Through a combination of random cDNA sequencing, degenerate polymerase chain reaction amplification, and low stringency hybridization we have identified six novel frizzled homologues from mammals, at least 11 from zebrafish, several from chicken and sea urchin, and one from Caenorhabditis elegans. The complete deduced amino acid sequences of the mammalian and nematode homologues share with the Drosophila frizzled protein a conserved amino-terminal cysteine-rich domain and seven putative transmembrane segments. Each of the mammalian homologues is expressed in a distinctive set of tissues in the adult, and at least three are expressed during embryogenesis. As hypothesized for the Drosophila frizzled protein, the frizzled homologues are likely to act as transmembrane receptors for as yet unidentified ligands. These observations predict the existence of a family of signal transduction pathways that are homologous to the pathway that determines tissue polarity in Drosophila.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Caenorhabditis elegans Central Nervous System/embryology,growth & development,metabolism Chickens Chromosome Mapping Cloning, Molecular DNA Primers DNA, Complementary Drosophila Proteins Drosophila melanogaster/genetics,metabolism Embryonic and Fetal Development Exons Frizzled Receptors Genes, Insect Humans In Situ Hybridization Insect Hormones/biosynthesis,chemistry Introns Mammals Membrane Proteins/biosynthesis,chemistry,genetics Mice Molecular Sequence Data Multigene Family Nematoda/metabolism Polymerase Chain Reaction Protein Structure, Secondary Rats Receptors, Cell Surface/biosynthesis,chemistry Receptors, G-Protein-Coupled/biosynthesis,chemistry Sea Urchins Sequence Homology, Amino Acid Zebrafish
Chemicals
DNA Primers DNA, Complementary Drosophila Proteins Frizzled Receptors Insect Hormones Membrane Proteins Receptors, Cell Surface Receptors, G-Protein-Coupled frizzled 8 protein, mouse fz protein, Drosophila
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Wang Y
Department of Molecular Biology, Howard Hughes Medical Institute, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Macke J P
Abella B S
Andreasson K
Worley P
Gilbert D J
Copeland N G
Jenkins N A
Nathans J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1996-02-23
Pages
4468-76
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
U43205, U43316, U43317, U43318, U43319, U43320, U43321, U49405, U49406, U49407, U49408, U49409, U49410, U49411, U49412, U49413, U49414, U49415, U49416, U49417
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