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Translational coupling and limited degradation of a polycistronic messenger modulate differential gene expression in the parD stability system of plasmid R1.
Ruiz-Echevarría, M J; de la Cueva, G; Díaz-Orejas, R.
Afiliación
  • Ruiz-Echevarría MJ; Centro de Investigaciones Biológicas (CSIC), Madrid, Spain.
Mol Gen Genet ; 248(5): 599-609, 1995 Sep 20.
Article en En | MEDLINE | ID: mdl-7476860
The parD stability system of plasmid R1 is an auto-regulated operon containing two genes, kis and kid, that code, respectively, for a killer protein (Kid) and for an antagonist of Kid action (Kis protein). A polycistronic transcript and a shorter mRNA, coding only for Kis and ending in a stem-loop sequence, have been identified as the main parD transcripts in cells carrying a derepressed parD operon. In this communication we show that both parD mRNAs have a half-life close to 1 min and are present in similar amounts. Using an assay based on cell-free extracts of Escherichia coli, we demonstrate that the short kis mRNA originates from limited degradation of the bicistronic parD transcript and that the stem-loop structure within the 5' end of the kid gene is specifically required for the formation of this short transcript. In vivo experiments show that synthesis of Kis is required for efficient synthesis of Kid. These data indicate that RNA processing and translational coupling are important mechanisms that modulate the differential expression of the two genes, kis and kid, in the bicistronic parD operon.
Asunto(s)
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Base de datos: MEDLINE Asunto principal: Plásmidos / Proteínas Bacterianas / ARN Mensajero / Regulación Bacteriana de la Expresión Génica / Procesamiento Postranscripcional del ARN / Proteínas de Escherichia coli / Proteínas de Unión al ADN Idioma: En Revista: Mol Gen Genet Año: 1995 Tipo del documento: Article País de afiliación: España
Buscar en Google
Base de datos: MEDLINE Asunto principal: Plásmidos / Proteínas Bacterianas / ARN Mensajero / Regulación Bacteriana de la Expresión Génica / Procesamiento Postranscripcional del ARN / Proteínas de Escherichia coli / Proteínas de Unión al ADN Idioma: En Revista: Mol Gen Genet Año: 1995 Tipo del documento: Article País de afiliación: España