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PMID: 2031187 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Effect of wnt-1 and related proteins on gap junctional communication in Xenopus embryos.

Science (New York, N.Y.) ·Vol. 252 ·No. 5009 ·1991-05-24 ·Pages 1173-6

Olson DJ, Christian JL, Moon RT

Abstract

The proto-oncogene wnt-1 (previously referred to as int-1) is thought to be important in embryonic pattern formation although its mechanisms of action are unknown. Premature and increased expression of the Wnt-1 protein, achieved by injection of synthetic wnt-1 RNA into fertilized Xenopus eggs, enhanced gap junctional communication between ventral cells of the developing embryo. This result is consistent with the hypothesis that Wnt proteins activate a receptor-mediated signal transduction pathway and that gap junctional communication can be a target of this pathway. The effects of two Wnt-1-related proteins on gap junctional communication were also investigated: overexpression of Xwnt-8 increased gap junctional coupling in a manner similar to Wnt-1, whereas Xwnt-5A did not. These findings are consistent with the existence of multiple receptors for Wnt proteins.

Related Genes
MeSH Terms
Animals Blastomeres/cytology,physiology Cell Communication Embryo, Nonmammalian/cytology,physiology Female Intercellular Junctions/physiology Male Protein-Tyrosine Kinases/genetics Proto-Oncogene Proteins/genetics,physiology Proto-Oncogenes Signal Transduction Sperm-Ovum Interactions Wnt Proteins Wnt1 Protein Xenopus Xenopus Proteins Zebrafish Proteins
Chemicals
Proto-Oncogene Proteins WNT1 protein, Xenopus Wnt Proteins Wnt1 Protein Xenopus Proteins Zebrafish Proteins wnt8a protein, Xenopus Protein-Tyrosine Kinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Olson D J
Department of Pharmacology, University of Washington, School of Medicine, Seattle 98195.
Christian J L
Moon R T
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1991-05-24
Pages
1173-6
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIDCR NIH HHS · DE-07023 · United States
NIAMS NIH HHS · KO4-AR01837 · United States
NIAMS NIH HHS · R01-AR40089 · United States
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