English   español  
Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/8244
Compartir / Impacto:
Estadísticas
Add this article to your Mendeley library MendeleyBASE
Citado 14 veces en Web of Knowledge®  |  Pub MebCentral Ver citas en PubMed Central  |  Ver citas en Google académico
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar otros formatos: Exportar EndNote (RIS)Exportar bibText (RIS)Exportar csv (RIS)
Título

Ribosomal P0 protein domain involved in selectivity of antifungal sordarin derivatives

AutorSantos, Cruz; Rodríguez-Gabriel, Miguel Ángel ; Remacha, Miguel; Ballesta, Juan P. G.
Palabras claveSaccharomyces cerevisiae
protein P0
Fecha de publicación2004
EditorAmerican Society for Microbiology
CitaciónAntimicrobial Agents and Chemotherapy, 2004, p. 2930-2936, Vol. 48, No. 8
ResumenThe ribosomal stalk protein P0 is involved in the susceptibility to the antifungal sordarin derivatives, as reported for a number of Saccharomyces cerevisiae resistant mutants. Mammals and some lower eukaryotes are naturally resistant to these compounds. It is shown here that expression in S. cerevisiae of the ribosomal protein P0 from Homo sapiens and from other sordarin-resistant organisms results in a decrease in the sensitivity of the cells to an agent of this class. To further characterize the P0 region responsible for inducing sordarin resistance, a series of protein chimeras containing complementary regions of the human and yeast P0 proteins were constructed and expressed in yeast. The chimeras complement the absence of the native yeast P0 except in chimeras containing the human P0 carboxyl-terminal domain. Resistance to sordarins was found to be associated with the presence of an HsP0 amino acid sequence comprising P118 to F138, which unexpectedly led to higher resistance than the presence of the complete human P0. A comparison of the corresponding region in P0 from yeast and sordarin-insensitive organisms, followed by site-directed mutagenesis, indicates that residues in positions 119, 124, and 126 have an important role in determining resistance to sordarins. Moreover, since sordarins block the eukaryotic elongation factor 2 (EF2) function, the P0 region affecting sordarin susceptibility must correspond to EF2-interacting domains of the ribosomal stalk protein, which affects the drug-binding site in the elongation factor
Versión del editorhttp://dx.doi.org/10.1128/AAC.48.8.2930-2936.2004
URIhttp://hdl.handle.net/10261/8244
DOI10.1128/AAC.48.8.2930-2936.2004
ISSN0066-4804 (print)
1098-6596 (online)
Aparece en las colecciones: (CBM) Artículos
Ficheros en este ítem:
Fichero Descripción Tamaño Formato  
CSantos_AntimAgentsChemother_2930.pdf270,64 kBAdobe PDFVista previa
Visualizar/Abrir
Mostrar el registro completo
 



NOTA: Los ítems de Digital.CSIC están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.