Evidence map›Paper›PMID 10022901›Full record

ArticleMolecular and cellular biology1999

Pseudouridine mapping in the Saccharomyces cerevisiae spliceosomal U small nuclear RNAs (snRNAs) reveals that pseudouridine synthase pus1p exhibits a dual substrate specificity for U2 snRNA and tRNA.

S Massenet, Y Motorin, D L Lafontaine, E C Hurt, H Grosjean, C Branlant

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

93 citing papers in PubMed, 143 citations in OpenAlex.

  1. Article
  2. Pseudouridylation landscape across 42bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The epitranscriptome of small non-coding RNAs.Non-coding RNA research · 2021
    Review
  12. Spliceosomal snRNA Epitranscriptomics.Frontiers in genetics · 2021
    Review
  13. Review
  14. Article
  15. Article
  16. Structural and functional modularity of the U2 snRNP in pre-mRNA splicing.Critical reviews in biochemistry and molecular biology · 2019
    Review
  17. Glycolytic flux inThe Biochemical journal · 2019
    Article
  18. Article
  19. Review
  20. Review

33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 3 countries.

S MassenetLaboratoire de Maturation des ARN et Enzymologie Moléculaire, UMR7567 CNRS-UHP, Faculté des Sciences, 54506 Vandoeuvre-les-Nancy Cédex, France.
Y Motorin
D L Lafontaine
E C Hurt
H Grosjean
C Branlant
Université de Lorraine · FRCentre National de la Recherche Scientifique · FRHeidelberg University · DELaboratoire d'Enzymologie et Biochimie Structurales · FRUniversity of Edinburgh · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudouridine (Psi) residues were localized in the Saccharomyces cerevisiae spliceosomal U small nuclear RNAs (UsnRNAs) by using the chemical mapping method. In contrast to vertebrate UsnRNAs, S. cerevisiae UsnRNAs contain only a few Psi residues, which are located in segments involved in intermolecular RNA-RNA or RNA-protein interactions. At these positions, UsnRNAs are universally modified. When yeast mutants disrupted for one of the several pseudouridine synthase genes (PUS1, PUS2, PUS3, and PUS4) or depleted in rRNA-pseudouridine synthase Cbf5p were tested for UsnRNA Psi content, only the loss of the Pus1p activity was found to affect Psi formation in spliceosomal UsnRNAs. Indeed, Psi44 formation in U2 snRNA was abolished. By using purified Pus1p enzyme and in vitro-produced U2 snRNA, Pus1p is shown here to catalyze Psi44 formation in the S. cerevisiae U2 snRNA. Thus, Pus1p is the first UsnRNA pseudouridine synthase characterized so far which exhibits a dual substrate specificity, acting on both tRNAs and U2 snRNA. As depletion of rRNA-pseudouridine synthase Cbf5p had no effect on UsnRNA Psi content, formation of Psi residues in S. cerevisiae UsnRNAs is not dependent on the Cbf5p-snoRNA guided mechanism.

Indexed as

PseudouridineRNA, FungalRNA, Small NuclearRNA, TransferSaccharomyces cerevisiae ProteinsBase SequenceCatalysisChromosome MappingFungal ProteinsHydro-LyasesIntramolecular TransferasesMolecular Sequence DataNucleic Acid ConformationRibonucleoprotein, U2 Small NuclearRNA PrecursorsRNA SplicingDEG1 protein, S cerevisiaeFungal ProteinsHydro-LyasesIntramolecular TransferasesPseudouridinepseudouridylate synthetaseRibonucleoprotein, U2 Small NuclearRNA, FungalRNA PrecursorsRNA, Small NuclearRNA, TransferSaccharomyces cerevisiae ProteinstRNA-pseudouridine synthase I

Identifiers

PMID10022901
PMCPMC84007
OpenAlexW2113738713

What OpenQuestion holds

Texttitle and abstract
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.