Functions of the exosome in rRNA, snoRNA and snRNA synthesis
Open Access
- 1 October 1999
- journal article
- research article
- Published by Springer Nature in The EMBO Journal
- Vol. 18 (19) , 5399-5410
- https://doi.org/10.1093/emboj/18.19.5399
Abstract
The yeast nuclear exosome contains multiple 3′→5′ exoribonucleases, raising the question of why so many activities are present in the complex. All components are required during the 3′ processing of the 5.8S rRNA, together with the putative RNA helicase Dob1p/Mtr4p. During this processing three distinct steps can be resolved, and hand‐over between different exonucleases appears to occur at least twice. 3′ processing of snoRNAs (small nucleolar RNAs) that are excised from polycistronic precursors or from mRNA introns is also a multi‐step process that involves the exosome, with final trimming specifically dependent on the Rrp6p component. The spliceosomal U4 snRNA (small nuclear RNA) is synthesized from a 3′ extended precursor that is cleaved by Rnt1p at sites 135 and 169 nt downstream of the mature 3′ end. This cleavage is followed by 3′→5′ processing of the pre‐snRNA involving the exosome complex and Dob1p. The exosome, together with Rnt1p, also participates in the 3′ processing of the U1 and U5 snRNAs. We conclude that the exosome is involved in the processing of many RNA substrates and that different components can have distinct functions.Keywords
This publication has 40 references indexed in Scilit:
- The yeast exosome and human PM-Scl are related complexes of 3' right-arrow 5' exonucleasesGenes & Development, 1999
- Depletion of yeast RNase III blocks correct U2 3' end formation and results in polyadenylated but functional U2 snRNAThe EMBO Journal, 1998
- Rrp6p, the Yeast Homologue of the Human PM-Scl 100-kDa Autoantigen, Is Essential for Efficient 5.8 S rRNA 3′ End FormationJournal of Biological Chemistry, 1998
- Alternative 3′-end processing of U5 snRNA by RNase IIIGenes & Development, 1997
- RNase III Cleaves Eukaryotic Preribosomal RNA at a U3 snoRNP-Dependent SiteCell, 1996
- Processing of fibrillarin-associated snoRNAs from pre-mRNA introns: An exonucleolytic process exclusively directed by the common stem-box terminal structureBiochimie, 1996
- TheXenopusintron-encoded U17 snoRNA is produced by exonucleolytic processing of its precursor in oocytesNucleic Acids Research, 1995
- In vitro study of processing of the intron-encoded U16 small nucleolar RNA in Xenopus laevis.Molecular and Cellular Biology, 1994
- A simple and efficient method for direct gene deletion inSaccharomyces cerevisiaeNucleic Acids Research, 1993
- Isolation and characterization of RAT1: an essential gene of Saccharomyces cerevisiae required for the efficient nucleocytoplasmic trafficking of mRNA.Genes & Development, 1992