Literature DB >> 8605882

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.

E Caffarelli1, A Fatica, S Prislei, E De Gregorio, P Fragapane, I Bozzoni.   

Abstract

A novel class of small nucleolar RNAs (snoRNAs), encoded in introns of protein coding genes and originating from processing of their precursor molecules, has recently been described. The L1 ribosomal protein (r-protein) gene of Xenopus laevis and its human homologue contain two snoRNAs, U16 and U18. It has been shown that these snoRNAs are excised from their intron precursors by endonucleolytic cleavage and that their processing is alternative to splicing. Two sequences, internal to the snoRNA coding region, have been identified as indispensable for processing the conserved boxes C and D. Competition experiments have shown that these sequences interact with diffusible factors which can bind both the pre-mRNA and the mature U16 snoRNA. Fibrillarin, which is known to associate with complexes formed on C and D boxes of other snoRNAs, is found in association with mature U16 RNA, as well as with its precursor molecules. This fact suggests that the complex formed on the pre-mRNA remains bound to U16 throughout all the processing steps. We also show that the complex formed on the C and D boxes is necessary to stabilize mature snoRNA.

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Year:  1996        PMID: 8605882      PMCID: PMC450010     

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


  38 in total

1.  The mechanisms controlling ribosomal protein L1 pre-mRNA splicing are maintained in evolution and rely on conserved intron sequences.

Authors:  S Prislei; S Sperandio; P Fragapane; E Caffarelli; C Presutti; I Bozzoni
Journal:  Nucleic Acids Res       Date:  1992-09-11       Impact factor: 16.971

2.  The U3 small nucleolar ribonucleoprotein functions in the first step of preribosomal RNA processing.

Authors:  S Kass; K Tyc; J A Steitz; B Sollner-Webb
Journal:  Cell       Date:  1990-03-23       Impact factor: 41.582

3.  Expression of the gene for ribosomal protein L1 in Xenopus embryos: alteration of gene dosage by microinjection.

Authors:  P Pierandrei-Amaldi; I Bozzoni; B Cardinali
Journal:  Genes Dev       Date:  1988-01       Impact factor: 11.361

4.  Depletion of U14 small nuclear RNA (snR128) disrupts production of 18S rRNA in Saccharomyces cerevisiae.

Authors:  H D Li; J Zagorski; M J Fournier
Journal:  Mol Cell Biol       Date:  1990-03       Impact factor: 4.272

5.  Expression of two Xenopus laevis ribosomal protein genes in injected frog oocytes. A specific splicing block interferes with the L1 RNA maturation.

Authors:  I Bozzoni; P Fragapane; F Annesi; P Pierandrei-Amaldi; F Amaldi; E Beccari
Journal:  J Mol Biol       Date:  1984-12-25       Impact factor: 5.469

6.  Oligoribonucleotide synthesis using T7 RNA polymerase and synthetic DNA templates.

Authors:  J F Milligan; D R Groebe; G W Witherell; O C Uhlenbeck
Journal:  Nucleic Acids Res       Date:  1987-11-11       Impact factor: 16.971

7.  A nuclear extract of Xenopus laevis oocytes that accurately transcribes 5S RNA genes.

Authors:  E H Birkenmeier; D D Brown; E Jordan
Journal:  Cell       Date:  1978-11       Impact factor: 41.582

8.  In vitro assembly of U1 snRNPs.

Authors:  J Hamm; M Kazmaier; I W Mattaj
Journal:  EMBO J       Date:  1987-11       Impact factor: 11.598

9.  The accumulation of mature RNA for the Xenopus laevis ribosomal protein L1 is controlled at the level of splicing and turnover of the precursor RNA.

Authors:  E Caffarelli; P Fragapane; C Gehring; I Bozzoni
Journal:  EMBO J       Date:  1987-11       Impact factor: 11.598

10.  U3, U8 and U13 comprise a new class of mammalian snRNPs localized in the cell nucleolus.

Authors:  K Tyc; J A Steitz
Journal:  EMBO J       Date:  1989-10       Impact factor: 11.598

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  71 in total

1.  The Rev protein is able to transport to the cytoplasm small nucleolar RNAs containing a Rev binding element.

Authors:  S B Buonomo; A Michienzi; F G De Angelis; I Bozzoni
Journal:  RNA       Date:  1999-08       Impact factor: 4.942

2.  Splicing-independent processing of plant box C/D and box H/ACA small nucleolar RNAs.

Authors:  D J Leader; G P Clark; J Watters; A F Beven; P J Shaw; J W Brown
Journal:  Plant Mol Biol       Date:  1999-04       Impact factor: 4.076

3.  Role of the box C/D motif in localization of small nucleolar RNAs to coiled bodies and nucleoli.

Authors:  A Narayanan; W Speckmann; R Terns; M P Terns
Journal:  Mol Biol Cell       Date:  1999-07       Impact factor: 4.138

4.  p62, a novel Xenopus laevis component of box C/D snoRNPs.

Authors:  D Filippini; I Bozzoni; E Caffarelli
Journal:  RNA       Date:  2000-03       Impact factor: 4.942

5.  Multiple conserved segments of E1 small nucleolar RNA are involved in the formation of a ribonucleoprotein particle in frog oocytes.

Authors:  D D Ruhl; M E Pusateri; G L Eliceiri
Journal:  Biochem J       Date:  2000-06-15       Impact factor: 3.857

6.  Nop58p is a common component of the box C+D snoRNPs that is required for snoRNA stability.

Authors:  D L Lafontaine; D Tollervey
Journal:  RNA       Date:  1999-03       Impact factor: 4.942

7.  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

8.  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

Review 9.  The 3' end formation in small RNAs.

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

Review 10.  Small nucleolar RNAs: versatile trans-acting molecules of ancient evolutionary origin.

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