Evidence map›Paper›PMID 11252721›Full record

ArticleEMBO reports2001

Fission yeast Prp4p kinase regulates pre-mRNA splicing by phosphorylating a non-SR-splicing factor.

W Schwelnus, K Richert, F Opitz, T Gross, Y Habara, T Tani, N F Käufer

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

W SchwelnusInstitute of Genetics, Technical University of Braunschweig, Germany.
K Richert
F Opitz
T Gross
Y Habara
T Tani
N F Käufer
Technische Universität Braunschweig · DEKyushu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We provide evidence that Prp4p kinase activity is required for pre-mRNA splicing in vivo and show that loss of activity impairs G1-S and G2-M progression in the cell cycle. Prp4p interacts genetically with the non-SR (serine/arginine) splicing factors Prp1p and Prp5p. Bacterially produced Prp1p is phosphorylated by Prp4p in vitro. Prp4p and Prp1p also interact in the yeast two-hybrid system. In vivo labelling studies using a strain with a mutant allele of the prp4 gene in the genetic background indicate a change in phosphorylation of the Prp1p protein. These results are consistent with the notion that Prp4p kinase is involved in the control of the formation of active spliceosomes, targeting non-SR splicing factors.

Indexed as

RNA SplicingSaccharomyces cerevisiae ProteinsSchizosaccharomyces pombe ProteinsAllelesDEAD-box RNA HelicasesFungal ProteinsG1 PhaseG2 PhaseMutagenesisMutationPhenotypePhosphorylationPlasmidsProtein BindingProtein Serine-Threonine KinasesRibonucleoprotein, U4-U6 Small NuclearDEAD-box RNA HelicasesFungal ProteinsProtein Serine-Threonine KinasesPRP1 protein, S pombeprp4 protein, S pombePRP5 protein, S cerevisiaeRibonucleoprotein, U4-U6 Small NuclearRNA HelicasesRNA, MessengerRNA Splicing FactorsSaccharomyces cerevisiae ProteinsSchizosaccharomyces pombe Proteins

Identifiers

PMID11252721
PMCPMC1083806
OpenAlexW2105856433

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.