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Armc8 is an evolutionarily conserved armadillo protein involved in cell-cell adhesion complexes through multiple molecular interactions.
Gul, Ismail Sahin; Hulpiau, Paco; Sanders, Ellen; van Roy, Frans; van Hengel, Jolanda.
Afiliación
  • Gul IS; Center for Inflammation Research, VIB, Ghent, Belgium.
  • Hulpiau P; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
  • Sanders E; Center for Inflammation Research, VIB, Ghent, Belgium.
  • van Roy F; Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
  • van Hengel J; Howest, University College West Flanders, Bruges, Belgium.
Biosci Rep ; 39(8)2019 08 30.
Article en En | MEDLINE | ID: mdl-30482882
ABSTRACT
Armadillo-repeat-containing protein 8 (Armc8) belongs to the family of armadillo-repeat containing proteins, which have been found to be involved in diverse cellular functions including cell-cell contacts and intracellular signaling. By comparative analyses of armadillo repeat protein structures and genomes from various premetazoan and metazoan species, we identified orthologs of human Armc8 and analyzed in detail the evolutionary relationship of Armc8 genes and their encoded proteins. Armc8 is a highly ancestral armadillo protein although not present in yeast. Consequently, Armc8 is not the human ortholog of yeast Gid5/Vid28.Further, we performed a candidate approach to characterize new protein interactors of Armc8. Interactions between Armc8 and specific δ-catenins (plakophilins-1, -2, -3 and p0071) were observed by the yeast two-hybrid approach and confirmed by co-immunoprecipitation and co-localization. We also showed that Armc8 interacts specifically with αE-catenin but neither with αN-catenin nor with αT-catenin. Degradation of αE-catenin has been reported to be important in cancer and to be regulated by Armc8. A similar process may occur with respect to plakophilins in desmosomes. Deregulation of desmosomal proteins has been considered to contribute to tumorigenesis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Adhesión Celular / Proteínas del Dominio Armadillo Límite: Humans Idioma: En Revista: Biosci Rep Año: 2019 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Adhesión Celular / Proteínas del Dominio Armadillo Límite: Humans Idioma: En Revista: Biosci Rep Año: 2019 Tipo del documento: Article País de afiliación: Bélgica
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