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Interaction between the reductase Tah18 and highly conserved Fe-S containing Dre2 C-terminus is essential for yeast viability.
Soler, Nicolas; Delagoutte, Emmanuelle; Miron, Simona; Facca, Céline; Baïlle, Dorothée; d'Autreaux, Benoit; Craescu, Gil; Frapart, Yves-Michel; Mansuy, Daniel; Baldacci, Giuseppe; Huang, Meng-Er; Vernis, Laurence.
Afiliación
  • Soler N; CNRS UMR2027 Institut Curie Centre de Recherche, Centre Universitaire, 91405 Orsay, France.
Mol Microbiol ; 82(1): 54-67, 2011 Oct.
Article en En | MEDLINE | ID: mdl-21902732
Tah18-Dre2 is a recently identified yeast protein complex, which is highly conserved in human and has been implicated in the regulation of oxidative stress induced cell death and in cytosolic Fe-S proteins synthesis. Tah18 is a diflavin oxido-reductase with binding sites for flavin mononucleotide, flavin adenine dinucleotide and nicotinamide adenine dinucleotide phosphate, which is able to transfer electrons to Dre2 Fe-S clusters. In this work we characterized in details the interaction between Tah18 and Dre2, and analysed how it conditions yeast viability. We show that Dre2 C-terminus interacts in vivo and in vitro with the flavin mononucleotide- and flavin adenine dinucleotide-binding sites of Tah18. Neither the absence of the electron donor nicotinamide adenine dinucleotide phosphate-binding domain in purified Tah18 nor the absence of Fe-S in aerobically purified Dre2 prevents the binding in vitro. In vivo, when this interaction is affected in a dre2 mutant, yeast viability is reduced. Conversely, enhancing artificially the interaction between mutated Dre2 and Tah18 restores cellular viability despite still reduced cytosolic Fe-S cluster biosynthesis. We conclude that Tah18-Dre2 interaction in vivo is essential for yeast viability. Our study may provide new insight into the survival/death switch involving this complex in yeast and in human cells.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxidorreductasas / Saccharomyces cerevisiae / Proteínas de Saccharomyces cerevisiae / Viabilidad Microbiana / Proteínas Hierro-Azufre Idioma: En Revista: Mol Microbiol Asunto de la revista: BIOLOGIA MOLECULAR / MICROBIOLOGIA Año: 2011 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxidorreductasas / Saccharomyces cerevisiae / Proteínas de Saccharomyces cerevisiae / Viabilidad Microbiana / Proteínas Hierro-Azufre Idioma: En Revista: Mol Microbiol Asunto de la revista: BIOLOGIA MOLECULAR / MICROBIOLOGIA Año: 2011 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido