Literature DB >> 9649442

Processing of a dicistronic small nucleolar RNA precursor by the RNA endonuclease Rnt1.

G Chanfreau1, G Rotondo, P Legrain, A Jacquier.   

Abstract

Small nucleolar RNAs (snoRNAs) are intron encoded or expressed from monocistronic independent transcription units, or, in the case of plants, from polycistronic clusters. We show that the snR190 and U14 snoRNAs from the yeast Saccharomyces cerevisiae are co-transcribed as a dicistronic precursor which is processed by the RNA endonuclease Rnt1, the yeast ortholog of bacterial RNase III. RNT1 disruption results in a dramatic decrease in the levels of mature U14 and snR190 and in accumulation of dicistronic snR190-U14 RNAs. Addition of recombinant Rnt1 to yeast extracts made from RNT1 disruptants induces the chase of dicistronic RNAs into mature snoRNAs, showing that dicistronic RNAs correspond to functional precursors stalled in the processing pathway. Rnt1 cleaves a dicistronic transcript in vitro in the absence of other factors, separating snR190 from U14. Thus, one of the functions of eukaryotic RNase III is, as for the bacterial enzyme, to liberate monocistronic RNAs from polycistronic transcripts.

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Year:  1998        PMID: 9649442      PMCID: PMC1170708          DOI: 10.1093/emboj/17.13.3726

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  53 in total

Review 1.  Trans-acting factors in yeast pre-rRNA and pre-snoRNA processing.

Authors:  D Lafontaine; D Tollervey
Journal:  Biochem Cell Biol       Date:  1995 Nov-Dec       Impact factor: 3.626

2.  Site-specific ribose methylation of preribosomal RNA: a novel function for small nucleolar RNAs.

Authors:  Z Kiss-László; Y Henry; J P Bachellerie; M Caizergues-Ferrer; T Kiss
Journal:  Cell       Date:  1996-06-28       Impact factor: 41.582

3.  RNase III cleaves eukaryotic preribosomal RNA at a U3 snoRNP-dependent site.

Authors:  S A Elela; H Igel; M Ares
Journal:  Cell       Date:  1996-04-05       Impact factor: 41.582

4.  U14 base-pairs with 18S rRNA: a novel snoRNA interaction required for rRNA processing.

Authors:  W Q Liang; M J Fournier
Journal:  Genes Dev       Date:  1995-10-01       Impact factor: 11.361

5.  Elements essential for processing intronic U14 snoRNA are located at the termini of the mature snoRNA sequence and include conserved nucleotide boxes C and D.

Authors:  N J Watkins; R D Leverette; L Xia; M T Andrews; E S Maxwell
Journal:  RNA       Date:  1996-02       Impact factor: 4.942

6.  Processing of the intron-encoded U16 and U18 snoRNAs: the conserved C and D boxes control both the processing reaction and the stability of the mature snoRNA.

Authors:  E Caffarelli; A Fatica; S Prislei; E De Gregorio; P Fragapane; I Bozzoni
Journal:  EMBO J       Date:  1996-03-01       Impact factor: 11.598

7.  Purification and characterization of the Pac1 ribonuclease of Schizosaccharomyces pombe.

Authors:  G Rotondo; D Frendewey
Journal:  Nucleic Acids Res       Date:  1996-06-15       Impact factor: 16.971

8.  An essential domain in Saccharomyces cerevisiae U14 snoRNA is absent in vertebrates, but conserved in other yeasts.

Authors:  D A Samarsky; G S Schneider; M J Fournier
Journal:  Nucleic Acids Res       Date:  1996-06-01       Impact factor: 16.971

9.  A mammalian gene with introns instead of exons generating stable RNA products.

Authors:  K T Tycowski; M D Shu; J A Steitz
Journal:  Nature       Date:  1996-02-01       Impact factor: 49.962

10.  Depletion of yeast RNase III blocks correct U2 3' end formation and results in polyadenylated but functional U2 snRNA.

Authors:  S Abou Elela; M Ares
Journal:  EMBO J       Date:  1998-07-01       Impact factor: 11.598

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  77 in total

Review 1.  Protein trans-acting factors involved in ribosome biogenesis in Saccharomyces cerevisiae.

Authors:  D Kressler; P Linder; J de La Cruz
Journal:  Mol Cell Biol       Date:  1999-12       Impact factor: 4.272

2.  Trans-complementation of the second step of pre-mRNA splicing by exogenous 5' exons.

Authors:  G Chanfreau; C Gouyette; B Schwer; A Jacquier
Journal:  RNA       Date:  1999-07       Impact factor: 4.942

3.  Substrate recognition by a eukaryotic RNase III: the double-stranded RNA-binding domain of Rnt1p selectively binds RNA containing a 5'-AGNN-3' tetraloop.

Authors:  R Nagel; M Ares
Journal:  RNA       Date:  2000-08       Impact factor: 4.942

4.  Multiple snoRNA gene clusters from Arabidopsis.

Authors:  J W Brown; G P Clark; D J Leader; C G Simpson; T Lowe
Journal:  RNA       Date:  2001-12       Impact factor: 4.942

5.  Release of U18 snoRNA from its host intron requires interaction of Nop1p with the Rnt1p endonuclease.

Authors:  C Giorgi; A Fatica; R Nagel; I Bozzoni
Journal:  EMBO J       Date:  2001-12-03       Impact factor: 11.598

6.  A novel family of RNA tetraloop structure forms the recognition site for Saccharomyces cerevisiae RNase III.

Authors:  H Wu; P K Yang; S E Butcher; S Kang; G Chanfreau; J Feigon
Journal:  EMBO J       Date:  2001-12-17       Impact factor: 11.598

Review 7.  The 3' end formation in small RNAs.

Authors:  Karthika Perumal; Ram Reddy
Journal:  Gene Expr       Date:  2002

Review 8.  Small nucleolar RNAs: versatile trans-acting molecules of ancient evolutionary origin.

Authors:  Michael P Terns; Rebecca M Terns
Journal:  Gene Expr       Date:  2002

Review 9.  RNA degradation and models for post-transcriptional gene-silencing.

Authors:  F Meins
Journal:  Plant Mol Biol       Date:  2000-06       Impact factor: 4.076

10.  Deletion of Rnt1p alters the proportion of open versus closed rRNA gene repeats in yeast.

Authors:  Mathieu Catala; Maxime Tremblay; Eric Samson; Antonio Conconi; Sherif Abou Elela
Journal:  Mol Cell Biol       Date:  2007-11-08       Impact factor: 4.272

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