Evidence map›Paper›PMID 15542855›Full record

ArticleMolecular and cellular biology2004

Yeast shuttling SR proteins Npl3p, Gbp2p, and Hrb1p are part of the translating mRNPs, and Npl3p can function as a translational repressor.

Merle Windgassen, Dorothée Sturm, Iván J Cajigas, Carlos I González, Matthias Seedorf, Holger Bastians, Heike Krebber

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

66 citing papers in PubMed, 120 citations in OpenAlex.

  1. UGA4 and YBR062C Regulate Oxidative Stress Tolerance Under Heavy Metal Toxicity.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  9. The RGG motif proteins: Interactions, functions, and regulations.Wiley interdisciplinary reviews. RNA · 2023
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  13. The Great Escape: mRNA Export through the Nuclear Pore Complex.International journal of molecular sciences · 2021
    Review
  14. Review
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  18. Review
  19. Article
  20. Article

6 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

7 authors at 3 institutions in 2 countries.

Merle WindgassenInstitut für Molekularbiologie und Tumorforschung der Philipps-Universität Marburg, Emil-Mannkopff-Str. 2, 35037 Marburg, Germany.
Dorothée Sturm
Iván J Cajigas
Carlos I González
Matthias Seedorf
Holger Bastians
Heike Krebber
Philipps University of Marburg · DEUniversity of Puerto Rico at Río Piedras · PRHeidelberg University · DE

Funding

POST-TRANSCRIPTIONAL CONTROL OF THE HEART AND LUNGSK01HL004355 · NHLBI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI GONZALEZ, CARLOS I · 2000 to 2004
$603k
NHLBI NIH HHS K01 HL004355NHLBI NIH HHS K01 HL-04355-02NIGMS NIH HHS GM008102-3052
6 · The paper itself

Abstract

A major challenge in current molecular biology is to understand how sequential steps in gene expression are coupled. Recently, much attention has been focused on the linkage of transcription, processing, and mRNA export. Here we describe the cytoplasmic rearrangement for shuttling mRNA binding proteins in Saccharomyces cerevisiae during translation. While the bulk of Hrp1p, Nab2p, or Mex67p is not associated with polysome containing mRNAs, significant amounts of the serine/arginine (SR)-type shuttling mRNA binding proteins Npl3p, Gbp2p, and Hrb1p remain associated with the mRNA-protein complex during translation. Interestingly, a prolonged association of Npl3p with polysome containing mRNAs results in translational defects, indicating that Npl3p can function as a negative translational regulator. Consistent with this idea, a mutation in NPL3 that slows down translation suppresses growth defects caused by the presence of translation inhibitors or a mutation in eIF5A. Moreover, using sucrose density gradient analysis, we provide evidence that the import receptor Mtr10p, but not the SR protein kinase Sky1p, is involved in the timely regulated release of Npl3p from polysome-associated mRNAs. Together, these data shed light onto the transformation of an exporting to a translating mRNP.

Indexed as

Protein BiosynthesisBiological TransportBlotting, NorthernCentrifugation, Density GradientCodon, NonsenseCycloheximideCytoplasmGene DeletionGreen Fluorescent ProteinsHeterogeneous-Nuclear RibonucleoproteinsMicroscopy, FluorescenceMutationNuclear ProteinsNucleic Acid HybridizationNucleocytoplasmic Transport ProteinsPlasmidsCodon, NonsenseCycloheximideGbp2 protein, S cerevisiaeGreen Fluorescent ProteinsHeterogeneous-Nuclear RibonucleoproteinsHrb1 protein, S cerevisiaeMTR10 protein, S cerevisiaeNPL3 protein, S cerevisiaeNuclear ProteinsNucleocytoplasmic Transport ProteinsPoly APoly(A)-Binding ProteinsProtein Serine-Threonine KinasesProtein Synthesis InhibitorsRNARNA-Binding ProteinsRNA, MessengerRNA, RibosomalSaccharomyces cerevisiae ProteinsSKY1 protein, S cerevisiaeSucrose

Identifiers

PMID15542855
PMCPMC529038
OpenAlexW2097116113

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.