Evidence map›Paper›PMID 35091090›Full record

ArticleMolecular & cellular proteomics : MCP2022

Proteomics Uncovers Novel Components of an Interactive Protein Network Supporting RNA Export in Trypanosomes.

Alexandre Haruo Inoue, Patricia Ferreira Domingues, Mariana Serpeloni, Priscila Mazzocchi Hiraiwa, Newton Medeiros Vidal, Erin R Butterfield, Ricardo Canavate Del Pino, Adriana Ludwig, Cordula Boehm, Mark C Field and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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  6. Proteomic data of theData in brief · 2024
    Article
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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

11 authors at 4 institutions in 4 countries.

Alexandre Haruo InoueInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Patricia Ferreira DominguesInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Mariana SerpeloniInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Priscila Mazzocchi HiraiwaInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Newton Medeiros VidalNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA.
Erin R ButterfieldSchool of Life Sciences, University of Dundee, Dundee, Scotland, UK.
Ricardo Canavate Del PinoSchool of Life Sciences, University of Dundee, Dundee, Scotland, UK.
Adriana LudwigInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil.
Cordula BoehmSchool of Life Sciences, University of Dundee, Dundee, Scotland, UK.
Mark C FieldSchool of Life Sciences, University of Dundee, Dundee, Scotland, UK; Biology Centre, University of South Bohemia, České Budějovice, Czech Republic. Electronic address: mfield@mac.com.
Andréa Rodrigues ÁvilaInstituto Carlos Chagas, FIOCRUZ, Curitiba, Paraná, Brazil. Electronic address: andrea.avila@fiocruz.br.
Fundação Carlos Chagas · BRUniversity of Dundee · GBNational Institutes of Health · USSewanee: The University of the South · US

Funding

Medical Research Council MR/N010558/1Wellcome TrustWellcome Trust 204697/Z/16/Z
6 · The paper itself

Abstract

In trypanosomatids, transcription is polycistronic and all mRNAs are processed by trans-splicing, with export mediated by noncanonical mechanisms. Although mRNA export is central to gene regulation and expression, few orthologs of proteins involved in mRNA export in higher eukaryotes are detectable in trypanosome genomes, necessitating direct identification of protein components. We previously described conserved mRNA export pathway components in Trypanosoma cruzi, including orthologs of Sub2, a component of the TREX complex, and eIF4AIII (previously Hel45), a core component of the exon junction complex (EJC). Here, we searched for protein interactors of both proteins using cryomilling and mass spectrometry. Significant overlap between TcSub2 and TceIF4AIII-interacting protein cohorts suggests that both proteins associate with similar machinery. We identified several interactions with conserved core components of the EJC and multiple additional complexes, together with proteins specific to trypanosomatids. Additional immunoisolations of kinetoplastid-specific proteins both validated and extended the superinteractome, which is capable of supporting RNA processing from splicing through to nuclear export and cytoplasmic events. We also suggest that only proteomics is powerful enough to uncover the high connectivity between multiple aspects of mRNA metabolism and to uncover kinetoplastid-specific components that create a unique amalgam to support trypanosome mRNA maturation.

Indexed as

ProteomicsTrypanosoma cruziActive Transport, Cell NucleusRNARNA SplicingRNA TransportRNAevolutiongene expressionmRNA exportproteomicstrypanosomes

Identifiers

PMID35091090
PMCPMC8938319
OpenAlexW4210796953

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.