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Suppressor mutations in Rpf2-Rrs1 or Rpl5 bypass the Cgr1 function for pre-ribosomal 5S RNP-rotation.
Thoms, Matthias; Mitterer, Valentin; Kater, Lukas; Falquet, Laurent; Beckmann, Roland; Kressler, Dieter; Hurt, Ed.
Afiliación
  • Thoms M; Biochemistry Centre, University of Heidelberg, Heidelberg, 69120, Germany. matthias.thoms@bzh.uni-heidelberg.de.
  • Mitterer V; Biochemistry Centre, University of Heidelberg, Heidelberg, 69120, Germany.
  • Kater L; Gene Center, University of Munich, Munich, 81377, Germany.
  • Falquet L; University of Fribourg and Swiss Institute of Bioinformatics, Fribourg, 1700, Switzerland.
  • Beckmann R; Gene Center, University of Munich, Munich, 81377, Germany.
  • Kressler D; University of Fribourg and Swiss Institute of Bioinformatics, Fribourg, 1700, Switzerland.
  • Hurt E; Biochemistry Centre, University of Heidelberg, Heidelberg, 69120, Germany. ed.hurt@bzh.uni-heidelberg.de.
Nat Commun ; 9(1): 4094, 2018 10 05.
Article en En | MEDLINE | ID: mdl-30291245
ABSTRACT
During eukaryotic 60S biogenesis, the 5S RNP requires a large rotational movement to achieve its mature position. Cryo-EM of the Rix1-Rea1 pre-60S particle has revealed the post-rotation stage, in which a gently undulating α-helix corresponding to Cgr1 becomes wedged between Rsa4 and the relocated 5S RNP, but the purpose of this insertion was unknown. Here, we show that cgr1 deletion in yeast causes a slow-growth phenotype and reversion of the pre-60S particle to the pre-rotation stage. However, spontaneous extragenic suppressors could be isolated, which restore growth and pre-60S biogenesis in the absence of Cgr1. Whole-genome sequencing reveals that the suppressor mutations map in the Rpf2-Rrs1 module and Rpl5, which together stabilize the unrotated stage of the 5S RNP. Thus, mutations in factors stabilizing the pre-rotation stage facilitate 5S RNP relocation upon deletion of Cgr1, but Cgr1 itself could stabilize the post-rotation stage.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Ribosómicas / Proteínas Nucleares / ARN Ribosómico 5S / Proteínas de Unión al ARN / Proteínas de Saccharomyces cerevisiae Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2018 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Ribosómicas / Proteínas Nucleares / ARN Ribosómico 5S / Proteínas de Unión al ARN / Proteínas de Saccharomyces cerevisiae Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2018 Tipo del documento: Article País de afiliación: Alemania
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