The ribotoxin α-sarcin can cleave the sarcin/ricin loop on late 60S pre-ribosomes

Autor: Olombrada, Miriam, Peña, Cohue, Rodríguez-Galán, Olga, Klingauf-Nerurkar, Purnima, Portugal-Calisto, Daniela, Oborská-Oplová, Michaela, Altvater, Martin, Gavilanes, José G, Martínez-del-Pozo, Álvaro, de la Cruz, Jesús, García-Ortega, Lucía, Panse, Vikram Govind
Přispěvatelé: University of Zurich, Swiss National Science Foundation, National Centres of Competence in Research (Switzerland), ETH Zurich, European Research Council, Olga Mayenfisch Foundation, European Commission, Ministerio de Economía y Competitividad (España), EMBO
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: Digital.CSIC. Repositorio Institucional del CSIC
instname
E-Prints Complutense. Archivo Institucional de la UCM
E-Prints Complutense: Archivo Institucional de la UCM
Universidad Complutense de Madrid
Nucleic Acids Research
Nucleic Acids Research, 48 (11)
DOI: 10.5167/uzh-190530
Popis: The ribotoxin α-sarcin belongs to a family of ribonucleases that cleave the sarcin/ricin loop (SRL), a critical functional rRNA element within the large ribosomal subunit (60S), thereby abolishing translation. Whether α-sarcin targets the SRL only in mature 60S subunits remains unresolved. Here, we show that, in yeast, α-sarcin can cleave SRLs within late 60S pre-ribosomes containing mature 25S rRNA but not nucleolar/nuclear 60S pre-ribosomes containing 27S pre-rRNA in vivo. Conditional expression of α-sarcin is lethal, but does not impede early pre-rRNA processing, nuclear export and the cytoplasmic maturation of 60S pre-ribosomes. Thus, SRL-cleaved containing late 60S pre-ribosomes seem to escape cytoplasmic proofreading steps. Polysome analyses revealed that SRL-cleaved 60S ribosomal subunits form 80S initiation complexes, but fail to progress to the step of translation elongation. We suggest that the functional integrity of a α-sarcin cleaved SRL might be assessed only during translation.
V.G.P. is supported by grants from the Swiss National Science Foundation; NCCR RNA & Disease; ETH Zurich, a Starting Grant Award [EURIBIO260676] from the European Research Council and the Olga Mayenfisch Stiftung; Spanish Ministry of Economy and Competitiveness (MINECO) and the European Union ERFD program [BFU2012-32404] to A.M.P., [BFU2016-75352-P] to J.d.l.C.; M.O. was recipient of an FPU predoctoral contract from the Spanish Ministry of Education and an EMBO short-stay fellowship. Funding for open access charge: Swiss National Science Foundation.
Databáze: OpenAIRE