Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1993 Oct;123(2):477-84.
doi: 10.1083/jcb.123.2.477.

Induction of a secondary body axis in Xenopus by antibodies to beta-catenin

Affiliations

Induction of a secondary body axis in Xenopus by antibodies to beta-catenin

P D McCrea et al. J Cell Biol. 1993 Oct.

Abstract

We have obtained evidence that a known intracellular component of the cadherin cell-cell adhesion machinery, beta-catenin, contributes to the development of the body axis in the frog Xenopus laevis. Vertebrate beta-catenin is homologous to the Drosophila segment polarity gene product armadillo, and to vertebrate plakoglobin (McCrea, P. D., C. W. Turck, and B. Gumbiner. 1991. Science (Wash. DC). 254: 1359-1361.). Beta-Catenin was found present in all Xenopus embryonic stages examined, and associated with C-cadherin, the major cadherin present in early Xenopus embryos. To test beta-catenin's function, affinity purified Fab fragments were injected into ventral blastomeres of developing four-cell Xenopus embryos. A dramatic phenotype, the duplication of the dorsoanterior embryonic axis, was observed. Furthermore, Fab injections were capable of rescuing dorsal features in UV-ventralized embryos. Similar phenotypes have been observed in misexpression studies of the Wnt and other gene products, suggesting that beta-catenin participates in a signaling pathway which specifies embryonic patterning.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Adv Morphog. 1973;10:1-39 - PubMed
    1. Development. 1991 Feb;111(2):315-25 - PubMed
    1. Cell. 1982 Oct;30(3):675-86 - PubMed
    1. J Cell Biol. 1986 Feb;102(2):457-68 - PubMed
    1. Dev Biol. 1988 May;127(1):64-77 - PubMed

Publication types

MeSH terms