Npa1p, a Component of Very Early Pre-60S Ribosomal Particles, Associates with a Subset of Small Nucleolar RNPs Required for Peptidyl Transferase Center Modification

Author:

Dez Christophe1,Froment Carine2,Noaillac-Depeyre Jacqueline1,Monsarrat Bernard2,Caizergues-Ferrer Michèle1,Henry Yves1

Affiliation:

1. Laboratoire de Biologie Moléculaire Eucaryote, UMR5099 CNRS-Université Paul Sabatier, IFR 109, 31062 Toulouse cedex 04

2. Plate-forme protéomique, Institut de Pharmacologie et de Biologie Structurale (CNRS UMR 5089), 31077 Toulouse cedex, France

Abstract

ABSTRACT We have identified a novel essential nucleolar factor required for the synthesis of 5.8S and 25S rRNAs termed Npa1p. In the absence of Npa1p, the pre-rRNA processing pathway leading to 5.8S and 25S rRNA production is perturbed such that the C2 cleavage within internal transcribed spacer 2 occurs prematurely. Npa1p accumulates in the immediate vicinity of the dense fibrillar component of the nucleolus and is predominantly associated with the 27SA2 pre-rRNA, the RNA component of the earliest pre-60S ribosomal particles. By mass spectrometry, we have identified the protein partners of Npa1p, which include eight putative helicases as well as the novel Npa2p factor. Strikingly, we also show that Npa1p can associate with a subset of H/ACA and C/D small nucleolar RNPs (snoRNPs) involved in the chemical modification of residues in the vicinity of the peptidyl transferase center. Our results suggest that 27SA2-containing pre-60S ribosomal particles are located at the interface between the dense fibrillar and the granular components of the nucleolus and that these particles can contain a subset of snoRNPs.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

Reference109 articles.

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5. Identification of a 60S Preribosomal Particle that Is Closely Linked to Nuclear Export

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