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Nucleic Acids Research, 2000, Vol. 28, No. 9 1941-1946
© 2000 Oxford University Press

Identification of the Saccharomyces cerevisiae RNA:pseudouridine synthase responsible for formation of {Psi}2819 in 21S mitochondrial ribosomal RNA

I. Ansmant, S. Massenet, H. Grosjean1, Y. Motorin1 and C. Branlant*

Laboratoire de Maturation des ARN et Enzymologie Moléculaire, UMR 7567 CNRS-UHP Nancy I, Faculté des Sciences, BP 239, 54506 Vandoeuvre-les-Nancy Cedex, France and 1Laboratoire d’Enzymologie et Biochimie Structurales, UPR CNRS, 1 avenue de la Terrasse, 91198 Gif-sur-Yvette, France

So far, four RNA:pseudouridine ({Psi})-synthases have been identified in yeast Saccharomyces cerevisiae. Together, they act on cytoplasmic and mitochondrial tRNAs, U2 snRNA and rRNAs from cytoplasmic ribosomes. However, RNA:{Psi}-synthases responsible for several U->{Psi} conversions in tRNAs and UsnRNAs remained to be identified. Based on conserved amino-acid motifs in already characterised RNA:{Psi}-synthases, four additional open reading frames (ORFs) encoding putative RNA:{Psi}-synthases were identified in S.cerevisiae. Upon disruption of one of them, the YLR165c ORF, we found that the unique {Psi} residue normally present in the fully matured mitochondrial rRNAs ({Psi}2819 in 21S rRNA) was missing, while {Psi} residues at all the tested pseudo­uridylation sites in cytoplasmic and mitochondrial tRNAs and in nuclear UsnRNAs were retained. The selective U->{Psi} conversion at position 2819 in mitochondrial 21S rRNA was restored when the deleted yeast strain was transformed by a plasmid expressing the wild-type YLR165c ORF. Complementation was lost after point mutation (D71->A) in the postulated active site of the YLR165c-encoded protein, indicating the direct role of the YLR165c protein in {Psi}2819 synthesis in mitochondrial 21S rRNA. Hence, for nomenclature homogeneity the YLR165c ORF was renamed PUS5 and the corresponding RNA:{Psi}-synthase Pus5p. As already noticed for other mitochondrial RNA modification enzymes, no canonical mitochondrial targeting signal was identified in Pus5p. Our results also show that {Psi}2819 in mitochondrial 21S rRNA is not essential for cell viability.

* To whom correspondence should be addressed. Tel: +33 3 83 91 20 92; Fax: +33 3 83 91 20 93; Email: christiane.branlant@maem.uhp-nancy.fr


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