Literature DB >> 9334335

Alternative 3'-end processing of U5 snRNA by RNase III.

G Chanfreau1, S A Elela, M Ares, C Guthrie.   

Abstract

The cellular components required to form the 3' ends of small nuclear RNAs are unknown. U5 snRNA from Saccharomyces cerevisiae is found in two forms that differ in length at their 3' ends (U5L and U5S). When added to a yeast cell free extract, synthetic pre-U5 RNA bearing downstream genomic sequences is processed efficiently and accurately to generate both mature forms of U5. The two forms of U5 are produced in vitro by alternative 3'-end processing. A temperature-sensitive mutation in the RNT1 gene encoding RNase III blocks accumulation of U5L in vivo. In vitro, alternative cleavage of the U5 precursor by RNase III determines the choice between the two multistep pathways that lead to U5L and U5S, one of which (U5L) is strictly dependent on RNase III. These results identify RNase III as a trans-acting factor involved in 3'-end formation of snRNA and show how RNase III might regulate alternative RNA processing pathways.

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Year:  1997        PMID: 9334335      PMCID: PMC316607          DOI: 10.1101/gad.11.20.2741

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  41 in total

1.  A gene from S. pombe with homology to E. coli RNAse III blocks conjugation and sporulation when overexpressed in wild type cells.

Authors:  H P Xu; M Riggs; L Rodgers; M Wigler
Journal:  Nucleic Acids Res       Date:  1990-09-11       Impact factor: 16.971

2.  Identification of functional U1 snRNA-pre-mRNA complexes committed to spliceosome assembly and splicing.

Authors:  B Seraphin; M Rosbash
Journal:  Cell       Date:  1989-10-20       Impact factor: 41.582

3.  Multiple roles for U6 snRNA in the splicing pathway.

Authors:  H D Madhani; R Bordonné; C Guthrie
Journal:  Genes Dev       Date:  1990-12       Impact factor: 11.361

4.  An RNA conformational change between the two chemical steps of group II self-splicing.

Authors:  G Chanfreau; A Jacquier
Journal:  EMBO J       Date:  1996-07-01       Impact factor: 11.598

5.  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

6.  Nucleocytoplasmic transport and processing of small nuclear RNA precursors.

Authors:  H E Neuman de Vegvar; J E Dahlberg
Journal:  Mol Cell Biol       Date:  1990-07       Impact factor: 4.272

Review 7.  Spliceosomal snRNAs.

Authors:  C Guthrie; B Patterson
Journal:  Annu Rev Genet       Date:  1988       Impact factor: 16.830

8.  Unexpected flexibility in an evolutionarily conserved protein-RNA interaction: genetic analysis of the Sm binding site.

Authors:  M H Jones; C Guthrie
Journal:  EMBO J       Date:  1990-08       Impact factor: 11.598

9.  A mutation in a single gene of Schizosaccharomyces pombe affects the expression of several snRNAs and causes defects in RNA processing.

Authors:  J Potashkin; D Frendewey
Journal:  EMBO J       Date:  1990-02       Impact factor: 11.598

10.  S. pombe pac1+, whose overexpression inhibits sexual development, encodes a ribonuclease III-like RNase.

Authors:  Y Iino; A Sugimoto; M Yamamoto
Journal:  EMBO J       Date:  1991-01       Impact factor: 11.598

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  61 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.  Reassembly and protection of small nuclear ribonucleoprotein particles by heat shock proteins in yeast cells.

Authors:  A P Bracken; U Bond
Journal:  RNA       Date:  1999-12       Impact factor: 4.942

3.  Three conserved members of the RNase D family have unique and overlapping functions in the processing of 5S, 5.8S, U4, U5, RNase MRP and RNase P RNAs in yeast.

Authors:  A van Hoof; P Lennertz; R Parker
Journal:  EMBO J       Date:  2000-03-15       Impact factor: 11.598

4.  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

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.  Solution structure of conserved AGNN tetraloops: insights into Rnt1p RNA processing.

Authors:  I Lebars; B Lamontagne; S Yoshizawa; S Aboul-Elela; D Fourmy
Journal:  EMBO J       Date:  2001-12-17       Impact factor: 11.598

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

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

9.  Transcription of the human U2 snRNA genes continues beyond the 3' box in vivo.

Authors:  P Cuello; D C Boyd; M J Dye; N J Proudfoot; S Murphy
Journal:  EMBO J       Date:  1999-05-17       Impact factor: 11.598

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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