Evidence map›Paper›PMID 40795994›Full record

ArticleOpen biology2025

Selective loss of ATP carriers in favour of SLC25A43 orthologues in metamonad mitochondria adapted to anaerobiosis.

Natalia Janowicz, Vít Dohnálek, Justyna Zítek, Priscila Peña-Diaz, Eva Pyrihová, Martin S King, Michaela Husová, Vojtěch Žárský, Edmund Kunji, Alena Zikova and 2 more

Abstract read
In one paragraph

Article in Open biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

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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

2 citing papers in PubMed.

  1. 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

12 authors.

Natalia JanowiczDepartment of Parasitology, BIOCEV, Charles University Faculty of Science, Prague, Czech Republic.
Vít DohnálekDepartment of Parasitology, BIOCEV, Charles University Faculty of Science, Prague, Czech Republic.ORCID 0000-0003-2928-1793
Justyna ZítekDepartment of Parasitology, BIOCEV, Charles University Faculty of Science, Prague, Czech Republic.
Priscila Peña-DiazDepartment of Parasitology, BIOCEV, Charles University Faculty of Science, Prague, Czech Republic.
Eva PyrihováDepartment of Chemistry, Bioscience Environmental Engineering, University of Stavanger, Stavanger, Norway.
Martin S KingMRC Mitochondrial Biology Unit, Cambridge Biomedical Campus, University of Cambridge, Cambridge, UK.
Michaela HusováInstitute of Parasitology, Biology Centre of the Czech Academy of Sciences, České Budějovice, Czech Republic.ORCID 0009-0006-1276-6793
Vojtěch ŽárskýDepartment of Parasitology, BIOCEV, Charles University Faculty of Science, Prague, Czech Republic.
Edmund KunjiMRC Mitochondrial Biology Unit, Cambridge Biomedical Campus, University of Cambridge, Cambridge, UK.
Alena ZikovaBiology Centre, Academy of Sciences of the Czech Republic, České Budějovice, Czech Republic.
Vladimír HamplDepartment of Parasitology, BIOCEV, Charles University Faculty of Science, Prague, Czech Republic.
Pavel DolezalDepartment of Parasitology, BIOCEV, Charles University Faculty of Science, Prague, Czech Republic.ORCID 0000-0003-1285-9026

Funding

European Regional Development Fund 'Centre for research of pathogenicity and virulence of parasites'European Research CouncilGordon and Betty Moore FoundationGrantová Agentura České RepublikyGrantová Agentura, Univerzita KarlovaMinisterstvo Školství, Mládeže a Tělovýchovy
6 · The paper itself

Abstract

Metamonada is a eukaryotic supergroup of free-living and parasitic anaerobic protists. Their characteristic feature is the presence of highly reduced mitochondria that have lost the ability to produce ATP by oxidative phosphorylation and in some cases even by substrate phosphorylation, with all ATP being imported from the cytosol. Given this striking difference in cellular ATP metabolism when compared to aerobic mitochondria, we studied the presence of mitochondrial carrier proteins (MCPs) mediating the transport of ATP across the inner mitochondrial membrane. Our bioinformatic analyses revealed remarkable reduction of MCP repertoire in Metamonada with striking loss of the major ADP/ATP carrier (AAC). Instead, nearly all species retained carriers orthologous to human SLC25A43 protein, a little-characterized MCP. Heterologous expression of metamonad SLC25A43 carriers confirmed their mitochondrial localization, and functional analysis revealed that SLC25A43 orthologues represent a distinct group of ATP transporters, which we designate as ATP-importing carriers (AIC). Together, our findings suggest that AIC facilitate the ATP import into highly reduced anaerobic mitochondria, compensating for their diminished or absent energy metabolism.

Indexed as

Adenosine TriphosphateMitochondriaMitochondrial ADP, ATP TranslocasesMitochondrial ProteinsAnaerobiosisHumansPhylogenyAdenosine TriphosphateMitochondrial ADP, ATP TranslocasesMitochondrial ProteinsADP/ATP carrierMetamonadamitochondrial carrier proteinmitochondrial evolutionmitochondrion-related organelleSLC25A43

Identifiers

PMID40795994
PMCPMC12343136

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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.