Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
???displayArticle.abstract???
Wnts are secreted signaling factors which influence cell fate and cell behavior in developing embryos. Overexpression in Xenopus laevis embryos of a Xenopus Wnt, Xwnt-8, leads to a duplication of the embryonic axis. In embryos ventralized by UV irradiation, Xwnt-8 restores expression of the putative transcription factor goosecoid, and rescues normal axis formation. In contrast, overexpression of Xwnt-5A in normal embryos generates defects in dorsoanterior structures, without inducing goosecoid or a secondary axis. To determine whether Xwnt-4 and Xwnt-11 fall into one of these two previously described classes of activity, synthetic mRNAs were introduced into animal caps, normal embryos, and UV-treated embryos. The results indicate that Xwnt-4, Xwnt-5A, and Xwnt-11 are members of a single functional class with activities that are indistinguishable in these assays. To investigate whether distinct regions of Xwnt-8 and Xwnt-5A were sufficient for eliciting the observed effects of overexpression, we generated a series of chimeric Xwnts. RNAs encoding the chimeras were injected into normal and UV-irradiated Xenopus embryos. Analysis of the embryonic phenotypes and goosecoid levels reveals that chimeras composed of carboxy-terminal regions of Xwnt-8 and amino-terminal regions of Xwnt-5A are indistinguishable from the activities of native Xwnt-8 and that are the reciprocal chimeras elicit effects indistinguishable from overexpression of native Xwnt-5A. We conclude that the carboxy-terminal halves of these Xwnts are candidate domains for specifying responses to Xwnt signals.
Baker,
Embryonic and imaginal requirements for wingless, a segment-polarity gene in Drosophila.
1988, Pubmed
Baker,
Embryonic and imaginal requirements for wingless, a segment-polarity gene in Drosophila.
1988,
Pubmed
Chakrabarti,
Secretory and inductive properties of Drosophila wingless protein in Xenopus oocytes and embryos.
1992,
Pubmed
,
Xenbase
Chomczynski,
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.
1987,
Pubmed
Christian,
Xwnt-8, a Xenopus Wnt-1/int-1-related gene responsive to mesoderm-inducing growth factors, may play a role in ventral mesodermal patterning during embryogenesis.
1991,
Pubmed
,
Xenbase
Couso,
Notch is required for wingless signaling in the epidermis of Drosophila.
1994,
Pubmed
Horton,
Gene splicing by overlap extension: tailor-made genes using the polymerase chain reaction.
1990,
Pubmed
Hume,
Cwnt-8C: a novel Wnt gene with a potential role in primitive streak formation and hindbrain organization.
1993,
Pubmed
,
Xenbase
Jue,
The mouse Wnt-1 gene can act via a paracrine mechanism in transformation of mammary epithelial cells.
1992,
Pubmed
Kao,
The entire mesodermal mantle behaves as Spemann's organizer in dorsoanterior enhanced Xenopus laevis embryos.
1988,
Pubmed
,
Xenbase
Kelly,
Histological preparation of Xenopus laevis oocytes and embryos.
1991,
Pubmed
,
Xenbase
Ku,
Xwnt-11: a maternally expressed Xenopus wnt gene.
1993,
Pubmed
,
Xenbase
Malacinski,
Association of an ultraviolet irradiation sensitive cytoplasmic localization with the future dorsal side of the amphibian egg.
1975,
Pubmed
Mason,
Mutational analysis of mouse Wnt-1 identifies two temperature-sensitive alleles and attributes of Wnt-1 protein essential for transformation of a mammary cell line.
1992,
Pubmed
McGrew,
Analysis of Xwnt-4 in embryos of Xenopus laevis: a Wnt family member expressed in the brain and floor plate.
1992,
Pubmed
,
Xenbase
McMahon,
The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain.
1990,
Pubmed
McMahon,
Ectopic expression of the proto-oncogene int-1 in Xenopus embryos leads to duplication of the embryonic axis.
1989,
Pubmed
,
Xenbase
Moon,
Dissecting Wnt signalling pathways and Wnt-sensitive developmental processes through transient misexpression analyses in embryos of Xenopus laevis.
1993,
Pubmed
,
Xenbase
Moon,
Xwnt-5A: a maternal Wnt that affects morphogenetic movements after overexpression in embryos of Xenopus laevis.
1993,
Pubmed
,
Xenbase
Morata,
The development of wingless, a homeotic mutation of Drosophila.
1977,
Pubmed
Nusse,
Wnt genes.
1992,
Pubmed
Olson,
Effect of wnt-1 and related proteins on gap junctional communication in Xenopus embryos.
1991,
Pubmed
,
Xenbase
Parkin,
Activity of Wnt-1 as a transmembrane protein.
1993,
Pubmed
,
Xenbase
Scharf,
Axis determination in eggs of Xenopus laevis: a critical period before first cleavage, identified by the common effects of cold, pressure and ultraviolet irradiation.
1983,
Pubmed
,
Xenbase
Smith,
Injected Xwnt-8 RNA acts early in Xenopus embryos to promote formation of a vegetal dorsalizing center.
1991,
Pubmed
,
Xenbase
Sokol,
Injected Wnt RNA induces a complete body axis in Xenopus embryos.
1991,
Pubmed
,
Xenbase
Steinbeisser,
Xenopus axis formation: induction of goosecoid by injected Xwnt-8 and activin mRNAs.
1993,
Pubmed
,
Xenbase
Stewart,
The anterior extent of dorsal development of the Xenopus embryonic axis depends on the quantity of organizer in the late blastula.
1990,
Pubmed
,
Xenbase
Thomas,
Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development.
1990,
Pubmed
Wolda,
Overlapping expression of Xwnt-3A and Xwnt-1 in neural tissue of Xenopus laevis embryos.
1993,
Pubmed
,
Xenbase
Wong,
Differential transformation of mammary epithelial cells by Wnt genes.
1994,
Pubmed