Evidence map›Paper›PMID 29287109›Full record

ArticlePLoS pathogens2017

Biogenesis of the mitochondrial DNA inheritance machinery in the mitochondrial outer membrane of Trypanosoma brucei.

Sandro Käser, Mathilde Willemin, Felix Schnarwiler, Bernd Schimanski, Daniel Poveda-Huertes, Silke Oeljeklaus, Beat Haenni, Benoît Zuber, Bettina Warscheid, Chris Meisinger and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

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  10. CRISPR-Cas9-Mediated Knock-In Approach to Insert the GFPMethods in molecular biology (Clifton, N.J.) · 2023
    Article
  11. Single p197 molecules of the mitochondrial genome segregation system ofProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Article
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  18. Review
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  20. Molecular model of the mitochondrial genome segregation machinery inProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
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 2 institutions in 2 countries.

Sandro KäserDepartment of Chemistry and Biochemistry, University of Bern, Bern, Switzerland.
Mathilde WilleminDepartment of Chemistry and Biochemistry, University of Bern, Bern, Switzerland.ORCID 0000-0001-6290-5444
Felix SchnarwilerDepartment of Chemistry and Biochemistry, University of Bern, Bern, Switzerland.
Bernd SchimanskiDepartment of Chemistry and Biochemistry, University of Bern, Bern, Switzerland.
Daniel Poveda-HuertesInstitute of Biochemistry and Molecular Biology, ZBMZ, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Silke OeljeklausDepartment of Biochemistry and Functional Proteomics, Faculty of Biology, University of Freiburg, Freiburg, Germany.
Beat HaenniInstitute of Anatomy, University of Bern, Bern, Switzerland.
Benoît ZuberInstitute of Anatomy, University of Bern, Bern, Switzerland.ORCID 0000-0001-7725-5579
Bettina WarscheidDepartment of Biochemistry and Functional Proteomics, Faculty of Biology, University of Freiburg, Freiburg, Germany.
Chris MeisingerInstitute of Biochemistry and Molecular Biology, ZBMZ, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
André SchneiderDepartment of Chemistry and Biochemistry, University of Bern, Bern, Switzerland.ORCID 0000-0001-5421-0909
University of Bern · CHUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria cannot form de novo but require mechanisms that mediate their inheritance to daughter cells. The parasitic protozoan Trypanosoma brucei has a single mitochondrion with a single-unit genome that is physically connected across the two mitochondrial membranes with the basal body of the flagellum. This connection, termed the tripartite attachment complex (TAC), is essential for the segregation of the replicated mitochondrial genomes prior to cytokinesis. Here we identify a protein complex consisting of three integral mitochondrial outer membrane proteins-TAC60, TAC42 and TAC40-which are essential subunits of the TAC. TAC60 contains separable mitochondrial import and TAC-sorting signals and its biogenesis depends on the main outer membrane protein translocase. TAC40 is a member of the mitochondrial porin family, whereas TAC42 represents a novel class of mitochondrial outer membrane β-barrel proteins. Consequently TAC40 and TAC42 contain C-terminal β-signals. Thus in trypanosomes the highly conserved β-barrel protein assembly machinery plays a major role in the biogenesis of its unique mitochondrial genome segregation system.

Indexed as

AnimalsDNA, KinetoplastDNA, MitochondrialGenome, MitochondrialGenome, ProtozoanHumansMitochondrial DynamicsMitochondrial MembranesMultiprotein ComplexesProtein Sorting SignalsProtozoan ProteinsTrypanosoma brucei bruceiDNA, KinetoplastDNA, MitochondrialMultiprotein ComplexesProtein Sorting SignalsProtozoan Proteins

Identifiers

PMID29287109
PMCPMC5764417
OpenAlexW2779684596

What OpenQuestion holds

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LicenceCC BY
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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.