Evidence map›Paper›PMID 17403781›Full record

ArticleGenes & development2007

Rearrangement of competing U2 RNA helices within the spliceosome promotes multiple steps in splicing.

Rhonda J Perriman, Manuel Ares

Abstract read
In one paragraph

Article in Genes & development, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
–field-weighted citation impact
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

78 citing papers in PubMed.

  1. The cellular landscape of druggable RNA-binding proteins.Nature reviews. Drug discovery · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Evolutionary conservation of RNA sequence and structure.Wiley interdisciplinary reviews. RNA · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Alternate RNA Structures.Cold Spring Harbor perspectives in biology · 2020
    Review
  17. Article
  18. Structural and functional modularity of the U2 snRNP in pre-mRNA splicing.Critical reviews in biochemistry and molecular biology · 2019
    Review
  19. Article
  20. Structural Basis of Nuclear pre-mRNA Splicing: Lessons from Yeast.Cold Spring Harbor perspectives in biology · 2019
    Review

18 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

2 authors.

Rhonda J PerrimanCenter for Molecular Biology of RNA Department of Molecular, Cell, and Developmental Biology, University of California at Santa Cruz, Santa Cruz, California 95064, USA. perriman@biology.ucsc.edu
Manuel Ares

Funding

STRUCTURE/FUNCTION OF YEAST SMALL NUCLEAR RNPSR01GM040478 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI ARES, MANUEL · 1988 to 2021
$10.8M
NIGMS NIH HHS GM 040478NIGMS NIH HHS R01 GM040478
6 · The paper itself

Abstract

Nuclear pre-messenger RNA (pre-mRNA) splicing requires multiple spliceosomal small nuclear RNA (snRNA) and pre-mRNA rearrangements. Here we reveal a new snRNA conformational switch in which successive roles for two competing U2 helices, stem IIa and stem IIc, promote distinct splicing steps. When stem IIa is stabilized by loss of stem IIc, rapid ATP-independent and Cus2p-insensitive prespliceosome formation occurs. In contrast, hyperstabilized stem IIc improves the first splicing step on aberrant branchpoint pre-mRNAs and rescues temperature-sensitive U6-U57C, a U6 mutation that also suppresses first-step splicing defects of branchpoint mutations. A second, later role for stem IIa is revealed by its suppression of a cold-sensitive allele of the second-step splicing factor PRP16. Our data expose a spliceosomal progression cycle of U2 stem IIa formation, disruption by stem IIc, and then reformation of stem IIa before the second catalytic step. We propose that the competing stem IIa and stem IIc helices are key spliceosomal RNA elements that optimize juxtaposition of the proper reactive sites during splicing.

Indexed as

RNA SplicingAdenosine TriphosphatasesBinding SitesCatalysisDEAD-box RNA HelicasesModels, BiologicalMutationNucleic Acid ConformationPhenotypeRNA-Binding ProteinsRNA HelicasesRNA PrecursorsRNA, Small NuclearRNA Splicing FactorsSaccharomyces cerevisiae ProteinsSpliceosomesAdenosine TriphosphatasesCUS2 protein, S cerevisiaeDEAD-box RNA HelicasesPRP16 protein, S cerevisiaePRP5 protein, S cerevisiaeRNA-Binding ProteinsRNA HelicasesRNA PrecursorsRNA, Small NuclearRNA Splicing FactorsSaccharomyces cerevisiae ProteinsTrans-ActivatorsU2 small nuclear RNA

Identifiers

PMID17403781
PMCPMC1838532

What OpenQuestion holds

Textmetadata
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.