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

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...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1993
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119835/
https://www.ncbi.nlm.nih.gov/pubmed/8408227
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collection PubMed
description 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.
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spelling pubmed-21198352008-05-01 Induction of a secondary body axis in Xenopus by antibodies to beta- catenin J Cell Biol Articles 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. The Rockefeller University Press 1993-10-02 /pmc/articles/PMC2119835/ /pubmed/8408227 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Induction of a secondary body axis in Xenopus by antibodies to beta- catenin
title Induction of a secondary body axis in Xenopus by antibodies to beta- catenin
title_full Induction of a secondary body axis in Xenopus by antibodies to beta- catenin
title_fullStr Induction of a secondary body axis in Xenopus by antibodies to beta- catenin
title_full_unstemmed Induction of a secondary body axis in Xenopus by antibodies to beta- catenin
title_short Induction of a secondary body axis in Xenopus by antibodies to beta- catenin
title_sort induction of a secondary body axis in xenopus by antibodies to beta- catenin
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2119835/
https://www.ncbi.nlm.nih.gov/pubmed/8408227