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Article

Analysis of Sequence and Structural Features That Identify the B/C Motif of U3 Small Nucleolar RNA as the Recognition Site for the Snu13p-Rrp9p Protein Pair

, , , &
Pages 1191-1206 | Received 14 Jul 2006, Accepted 20 Nov 2006, Published online: 27 Mar 2023
 

Abstract

The eukaryal Snu13p/15.5K protein binds K-turn motifs in U4 snRNA and snoRNAs. Two Snu13p/15.5K molecules bind the nucleolar U3 snoRNA required for the early steps of preribosomal processing. Binding of one molecule on the C′/D motif allows association of proteins Nop1p, Nop56p, and Nop58p, whereas binding of the second molecule on the B/C motif allows Rrp9p recruitment. To understand how the Snu13p-Rrp9p pair recognizes the B/C motif, we first improved the identification of RNA determinants required for Snu13p binding by experiments using the systematic evolution of ligands by exponential enrichment. This demonstrated the importance of a U·U pair stacked on the sheared pairs and revealed a direct link between Snu13p affinity and the stability of helices I and II. Sequence and structure requirements for efficient association of Rrp9p on the B/C motif were studied in yeast cells by expression of variant U3 snoRNAs and immunoselection assays. A G-C pair in stem II, a G residue at position 1 in the bulge, and a short stem I were found to be required. The data identify the in vivo function of most of the conserved residues of the U3 snoRNA B/C motif. They bring important information to understand how different K-turn motifs can recruit different sets of proteins after Snu13p association.

SUPPLEMENTAL MATERIAL

V. Igel-Bourguignon is acknowledged for her excellent technical assistance. B. Charpentier is acknowledged for helpful discussion. We thank S. Sonkaria for careful reading of the manuscript.

A.C. was a fellow from the French Ministère de la Recherche et des Nouvelles Technologies. This work was supported by the Centre National de la Recherche Scientifique; the French Ministère de la Recherche et des Nouvelles Technologies; the ACI Biologie Cellulaire, Moléculaire et Structurale, grant BCMS226; and the PRST Bioingénierie of the Conseil Régional Lorrain.

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