An α- <i>E-catenin</i> gene trap mutation defines its function in preimplantation development
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- Miguel Torres
- Abteilung Molekulare Zellbiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen 37077, Germany; and Abteilung Molekulare Embryologie, Max-Planck-Institut für Immunbiologie, Freiburg 79108, Germany
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- Anastassia Stoykova
- Abteilung Molekulare Zellbiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen 37077, Germany; and Abteilung Molekulare Embryologie, Max-Planck-Institut für Immunbiologie, Freiburg 79108, Germany
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- Otmar Huber
- Abteilung Molekulare Zellbiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen 37077, Germany; and Abteilung Molekulare Embryologie, Max-Planck-Institut für Immunbiologie, Freiburg 79108, Germany
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- Kamal Chowdhury
- Abteilung Molekulare Zellbiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen 37077, Germany; and Abteilung Molekulare Embryologie, Max-Planck-Institut für Immunbiologie, Freiburg 79108, Germany
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- Paolo Bonaldo
- Abteilung Molekulare Zellbiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen 37077, Germany; and Abteilung Molekulare Embryologie, Max-Planck-Institut für Immunbiologie, Freiburg 79108, Germany
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- Ahmed Mansouri
- Abteilung Molekulare Zellbiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen 37077, Germany; and Abteilung Molekulare Embryologie, Max-Planck-Institut für Immunbiologie, Freiburg 79108, Germany
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- Stefan Butz
- Abteilung Molekulare Zellbiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen 37077, Germany; and Abteilung Molekulare Embryologie, Max-Planck-Institut für Immunbiologie, Freiburg 79108, Germany
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- Rolf Kemler
- Abteilung Molekulare Zellbiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen 37077, Germany; and Abteilung Molekulare Embryologie, Max-Planck-Institut für Immunbiologie, Freiburg 79108, Germany
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- Peter Gruss
- Abteilung Molekulare Zellbiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen 37077, Germany; and Abteilung Molekulare Embryologie, Max-Planck-Institut für Immunbiologie, Freiburg 79108, Germany
説明
<jats:p> Catenins are proteins associated with the cytoplasmic domain of cadherins, a family of transmembrane cell adhesion molecules. The cadherin–catenin adhesion system is involved in morphogenesis during development and in the maintenance of the integrity of different tissue types. Using a gene trap strategy, we have isolated a mouse mutation for the gene encoding the α-E-catenin. This form of the α-catenin appears frequently coexpressed with E-cadherin in epithelial cell types. The mutation obtained eliminates the carboxyl-terminal third of the protein but nevertheless provokes a complete loss-of-function phenotype. Homozygous mutants show disruption of the trophoblast epithelium (the first differentiated embryonic tissue), and development is consequently blocked at the blastocyst stage. This phenotype parallels the defects observed in E-cadherin mutant embryos. Our results show the requirement of the α-E-catenin carboxy terminus for its function and represent evidence of the role of the α-E-catenin <jats:italic>in vivo</jats:italic> , identifying this molecule as the natural partner of the E-cadherin in trophoblast epithelium. </jats:p>
収録刊行物
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- Proceedings of the National Academy of Sciences
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Proceedings of the National Academy of Sciences 94 (3), 901-906, 1997-02-04
Proceedings of the National Academy of Sciences