Evidence map›Paper›PMID 37400497›Full record

ArticleNature cell biology2023

Arf1 coordinates fatty acid metabolism and mitochondrial homeostasis.

Ludovic Enkler, Viktoria Szentgyörgyi, Mirjam Pennauer, Cristina Prescianotto-Baschong, Isabelle Riezman, Aneta Wiesyk, Reut Ester Avraham, Martin Spiess, Einat Zalckvar, Roza Kucharczyk and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Nature cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
11.7field-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

46 citing papers in PubMed, 64 citations in OpenAlex.

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  18. RUNX2 cooperates with SREBP1 to rewire cancer metabolism and promote aggressiveness.Journal of experimental & clinical cancer research : CR · 2025
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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 at 4 institutions in 3 countries.

Ludovic EnklerBiozentrum, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0003-0505-2427
Viktoria SzentgyörgyiBiozentrum, University of Basel, Basel, Switzerland.
Mirjam PennauerBiozentrum, University of Basel, Basel, Switzerland.
Cristina Prescianotto-BaschongBiozentrum, University of Basel, Basel, Switzerland.
Isabelle RiezmanDepartment of Biochemistry, NCCR Chemical Biology, University of Geneva, Geneva, Switzerland.
Aneta WiesykInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Reut Ester AvrahamDepartment of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
Martin SpiessBiozentrum, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0001-7139-0550
Einat ZalckvarDepartment of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
Roza KucharczykInstitute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.
Howard RiezmanDepartment of Biochemistry, NCCR Chemical Biology, University of Geneva, Geneva, Switzerland.ORCID http://orcid.org/0000-0003-4680-9422
Anne SpangBiozentrum, University of Basel, Basel, Switzerland. anne.spang@unibas.ch.ORCID http://orcid.org/0000-0002-2387-6203
University of Basel · CHInstitute of Biochemistry and Biophysics, Polish Academy of Sciences · PLUniversity of Geneva · CHWeizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid mobilization through fatty acid β-oxidation is a central process essential for energy production during nutrient shortage. In yeast, this catabolic process starts in the peroxisome from where β-oxidation products enter mitochondria and fuel the tricarboxylic acid cycle. Little is known about the physical and metabolic cooperation between these organelles. Here we found that expression of fatty acid transporters and of the rate-limiting enzyme involved in β-oxidation is decreased in cells expressing a hyperactive mutant of the small GTPase Arf1, leading to an accumulation of fatty acids in lipid droplets. Consequently, mitochondria became fragmented and ATP synthesis decreased. Genetic and pharmacological depletion of fatty acids phenocopied the arf1 mutant mitochondrial phenotype. Although β-oxidation occurs in both mitochondria and peroxisomes in mammals, Arf1's role in fatty acid metabolism is conserved. Together, our results indicate that Arf1 integrates metabolism into energy production by regulating fatty acid storage and utilization, and presumably organelle contact sites.

Indexed as

MitochondriaPeroxisomesAnimalsFatty AcidsHomeostasisLipid MetabolismMammalsOxidation-ReductionFatty Acids

Identifiers

PMID37400497
PMCPMC10415182
OpenAlexW4382989553

What OpenQuestion holds

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LicenceCC BY
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.