Evidence map›Paper›PMID 15565172›Full record

ArticleThe EMBO journal2004

Proteomic analysis identifies a new complex required for nuclear pre-mRNA retention and splicing.

Andrzej Dziembowski, Ana-Paula Ventura, Berthold Rutz, Friederike Caspary, Céline Faux, Frédéric Halgand, Olivier Laprévote, Bertrand Séraphin

Abstract read
In one paragraph

Article in The EMBO journal, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing 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

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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

102 citing papers in PubMed.

  1. Review
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  3. Exploring Disordered Regions of Human Spliceosome Proteins.The journal of physical chemistry letters · 2026
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42 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

8 authors.

Andrzej DziembowskiCentre de Génétique Moléculaire, Avenue de la Terrasse, Gif sur Yvette, France.
Ana-Paula Ventura
Berthold Rutz
Friederike Caspary
Céline Faux
Frédéric Halgand
Olivier Laprévote
Bertrand Séraphin

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using the proteomic tandem affinity purification (TAP) method, we have purified the Saccharomyces cerevisie U2 snRNP-associated splicing factors SF3a and SF3b. While SF3a purification revealed only the expected subunits Prp9p, Prp11p and Prp21p, yeast SF3b was found to contain only six subunits, including previously known components (Rse1p, Hsh155p, Cus1p, Hsh49p), the recently identified Rds3p factor and a new small essential protein (Ysf3p) encoded by an unpredicted split ORF in the yeast genome. Surprisingly, Snu17p, the proposed yeast orthologue of the seventh human SF3b subunit, p14, was not found in the yeast complex. TAP purification revealed that Snu17p, together with Bud13p and a newly identified factor, Pml1p/Ylr016c, form a novel trimeric complex. Subunits of this complex were not essential for viability. However, they are required for efficient splicing in vitro and in vivo. Furthermore, inactivation of this complex causes pre-mRNA leakage from the nucleus. The corresponding complex was named pre-mRNA REtention and Splicing (RES). The presence of RES subunit homologues in numerous eukaryotes suggests that its function is evolutionarily conserved.

Indexed as

RNA SplicingAmino Acid SequenceCell NucleusHumansMacromolecular SubstancesMolecular Sequence DataPhylogenyProtein SubunitsProteomeRibonucleoprotein, U2 Small NuclearRNA PrecursorsSaccharomyces cerevisiae ProteinsSequence AlignmentMacromolecular SubstancesProtein SubunitsProteomeRibonucleoprotein, U2 Small NuclearRNA PrecursorsSaccharomyces cerevisiae Proteins

Identifiers

PMID15565172
PMCPMC535094

What OpenQuestion holds

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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.