Evidence map›Paper›PMID 25616281›Full record

ArticleEukaryotic cell2015

The ADP/ATP carrier and its relationship to oxidative phosphorylation in ancestral protist trypanosoma brucei.

Anna Gnipová, Karolína Šubrtová, Brian Panicucci, Anton Horváth, Julius Lukeš, Alena Zíková

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 25 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

6 authors at 4 institutions in 3 countries.

Anna GnipováBiology Center, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic Department of Biochemistry, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia.
Karolína ŠubrtováBiology Center, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic Faculty of Science, University of South Bohemia, České Budějovice, Czech Republic.
Brian PanicucciBiology Center, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic.
Anton HorváthDepartment of Biochemistry, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia.
Julius LukešBiology Center, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic Faculty of Science, University of South Bohemia, České Budějovice, Czech Republic Canadian Institute for Advanced Research, Toronto, Ontario, Canada.
Alena ZíkováBiology Center, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic Faculty of Science, University of South Bohemia, České Budějovice, Czech Republic azikova@paru.cas.cz.
Czech Academy of Sciences · CZCanadian Institute for Advanced Research · CAComenius University Bratislava · SKInstitute of Parasitology · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The highly conserved ADP/ATP carrier (AAC) is a key energetic link between the mitochondrial (mt) and cytosolic compartments of all aerobic eukaryotic cells, as it exchanges the ATP generated inside the organelle for the cytosolic ADP. Trypanosoma brucei, a parasitic protist of medical and veterinary importance, possesses a single functional AAC protein (TbAAC) that is related to the human and yeast ADP/ATP carriers. However, unlike previous studies performed with these model organisms, this study showed that TbAAC is most likely not a stable component of either the respiratory supercomplex III+IV or the ATP synthasome but rather functions as a physically separate entity in this highly diverged eukaryote. Therefore, TbAAC RNA interference (RNAi) ablation in the insect stage of T. brucei does not impair the activity or arrangement of the respiratory chain complexes. Nevertheless, RNAi silencing of TbAAC caused a severe growth defect that coincides with a significant reduction of mt ATP synthesis by both substrate and oxidative phosphorylation. Furthermore, TbAAC downregulation resulted in a decreased level of cytosolic ATP, a higher mt membrane potential, an elevated amount of reactive oxygen species, and a reduced consumption of oxygen in the mitochondria. Interestingly, while TbAAC has previously been demonstrated to serve as the sole ADP/ATP carrier for ADP influx into the mitochondria, our data suggest that a second carrier for ATP influx may be present and active in the T. brucei mitochondrion. Overall, this study provides more insight into the delicate balance of the functional relationship between TbAAC and the oxidative phosphorylation (OXPHOS) pathway in an early diverged eukaryote.

Indexed as

Evolution, MolecularOxidative PhosphorylationMitochondrial ADP, ATP TranslocasesProtozoan ProteinsTrypanosoma brucei bruceiMitochondrial ADP, ATP TranslocasesProtozoan Proteins

Identifiers

PMID25616281
PMCPMC4346568
OpenAlexW2009237120

What OpenQuestion holds

Textmetadata
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Registered trials

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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.