Evidence map›Paper›PMID 19061648›Full record

ArticleMolecular cell2008

A genetic interaction map of RNA-processing factors reveals links between Sem1/Dss1-containing complexes and mRNA export and splicing.

Gwendolyn M Wilmes, Megan Bergkessel, Sourav Bandyopadhyay, Michael Shales, Hannes Braberg, Gerard Cagney, Sean R Collins, Gregg B Whitworth, Tracy L Kress, Jonathan S Weissman and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 176 papers.

0numbers the graph read from it
0cells of the map it votes in
176citing papers in PubMed
12.4field-weighted citation impact, top 1% 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

176 citing papers in PubMed, 259 citations in OpenAlex.

  1. Article
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  7. Review
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  9. Article
  10. Structures and mRNP remodeling mechanism of the TREX-2 complex.Structure (London, England : 1993) · 2025
    Article
  11. Point Mutations in the M Domain of PCID2 Impair Its Function in mRNA Export in Drosophila melanogaster.Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections · 2024
    Article
  12. Review
  13. Article
  14. PCID2 Subunit of theCurrent issues in molecular biology · 2023
    Article
  15. Article
  16. CRISPR/Cas9-Targeted Disruption of Two Highly HomologousInternational journal of molecular sciences · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Article

116 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

13 authors at 4 institutions in 2 countries.

Gwendolyn M WilmesDepartment of Biochemistry and Biophysics, University of California, San Francisco, 600 16th Street, Genentech Hall, San Francisco, CA 94143-2200, USA.
Megan Bergkessel
Sourav Bandyopadhyay
Michael Shales
Hannes Braberg
Gerard Cagney
Sean R Collins
Gregg B Whitworth
Tracy L Kress
Jonathan S Weissman
Trey Ideker
Christine Guthrie
Nevan J Krogan
University of California, San Francisco · USQB3 · USLa Jolla Bioengineering Institute · USUniversity of California San Diego · US

Funding

BIOSYNTHESIS OF RNASR01GM021119 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GUTHRIE, CHRISTINE · 1985 to 2015
$12.9M
BIOSYNTHESIS OF RNASR37GM021119 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI GUTHRIE, CHRISTINE · 1990 to 1999
–
Howard Hughes Medical InstituteNIGMS NIH HHS GM21119NIGMS NIH HHS R01 GM021119NIGMS NIH HHS R37 GM021119
6 · The paper itself

Abstract

We used a quantitative, high-density genetic interaction map, or E-MAP (Epistatic MiniArray Profile), to interrogate the relationships within and between RNA-processing pathways. Due to their complexity and the essential roles of many of the components, these pathways have been difficult to functionally dissect. Here, we report the results for 107,155 individual interactions involving 552 mutations, 166 of which are hypomorphic alleles of essential genes. Our data enabled the discovery of links between components of the mRNA export and splicing machineries and Sem1/Dss1, a component of the 19S proteasome. In particular, we demonstrate that Sem1 has a proteasome-independent role in mRNA export as a functional component of the Sac3-Thp1 complex. Sem1 also interacts with Csn12, a component of the COP9 signalosome. Finally, we show that Csn12 plays a role in pre-mRNA splicing, which is independent of other signalosome components. Thus, Sem1 is involved in three separate and functionally distinct complexes.

Indexed as

Protein Interaction MappingRNA Processing, Post-TranscriptionalRNA SplicingRNA TransportCOP9 Signalosome ComplexExoribonucleasesModels, BiologicalMultiprotein ComplexesPeptide HydrolasesProteasome Endopeptidase ComplexRNA, MessengerSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCOP9 Signalosome ComplexDSS1 protein, S cerevisiaeExoribonucleasesMultiprotein ComplexesPeptide HydrolasesProteasome Endopeptidase ComplexRNA, MessengerSaccharomyces cerevisiae ProteinsSEM1 protein, S cerevisiae

Identifiers

PMID19061648
PMCPMC2644724
OpenAlexW2015881243

What OpenQuestion holds

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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.