Evidence map›Paper›PMID 32804083›Full record

ArticleeLife2020

Mitochondrial fatty acid synthesis coordinates oxidative metabolism in mammalian mitochondria.

Sara M Nowinski, Ashley Solmonson, Scott F Rusin, J Alan Maschek, Claire L Bensard, Sarah Fogarty, Mi-Young Jeong, Sandra Lettlova, Jordan A Berg, Jeffrey T Morgan and 9 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

79 citing papers in PubMed, 139 citations in OpenAlex.

  1. Article
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  15. Targeted Metabolomic Methods forJournal of proteome research · 2025
    Article
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19 more citing papers are in PubMed but not listed here.

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

19 authors at 4 institutions in 1 country.

Sara M NowinskiDepartment of Biochemistry, Salt Lake City, United States.ORCID 0000-0002-4744-6101
Ashley SolmonsonChildren's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0001-8863-4558
Scott F RusinDepartment of Cell Biology, Harvard University School of Medicine, Boston, United States.
J Alan MaschekDiabetes & Metabolism Research Center, Salt Lake City, United States.
Claire L BensardDepartment of Biochemistry, Salt Lake City, United States.
Sarah FogartyDepartment of Biochemistry, Salt Lake City, United States.
Mi-Young JeongDepartment of Biochemistry, Salt Lake City, United States.
Sandra LettlovaDepartment of Biochemistry, Salt Lake City, United States.
Jordan A BergDepartment of Biochemistry, Salt Lake City, United States.
Jeffrey T MorganDepartment of Biochemistry, Salt Lake City, United States.
Yeyun OuyangDepartment of Biochemistry, Salt Lake City, United States.
Bradley C NaylorMetabolomics, Proteomics and Mass Spectrometry Core Research Facilities University of Utah, Salt Lake City, United States.
Joao A PauloDepartment of Cell Biology, Harvard University School of Medicine, Boston, United States.
Katsuhiko FunaiDiabetes & Metabolism Research Center, Salt Lake City, United States.
James E CoxDepartment of Biochemistry, Salt Lake City, United States.
Steven P GygiDepartment of Cell Biology, Harvard University School of Medicine, Boston, United States.
Dennis R WingeDepartment of Biochemistry, Salt Lake City, United States.ORCID 0000-0003-1160-1189
Ralph J DeBerardinisChildren's Medical Center Research Institute, University of Texas Southwestern Medical Center, Dallas, United States.
Jared RutterDepartment of Biochemistry, Salt Lake City, United States.ORCID 0000-0002-2710-9765
Harvard University · USHoward Hughes Medical Institute · USUniversity of Utah · USChildren's Medical Center · US

Funding

TRAINING IN CARDIOVASCULAR RESEARCHT32HL007576 · NHLBI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Stavros George Drakos, Robin M Shaw · 1985 to 2026
$10.6M
New Sample Multiplexing Technologies to Identify Chemical Probes and Illuminate Ubiquitin BiologyR01GM067945 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GYGI, STEVEN P · 2003 to 2024
$10.5M
Metabolic Regulators of Tumor Growth and ProgressionR35CA220449 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI RALPH J DEBERARDINIS · 2017 to 2026
$9.4M
Proteomics CoreU54DK110858 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Anna E Beaudin, JAMES Eric COX · 2016 to 2026
$8.6M
PE methylation in skeletal muscle energy efficiencyR01DK107397 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI FUNAI, KATSUHIKO · 2017 to 2025
$3.8M
Mitochondrial Biochemistry: From Mechanisms to DiseaseR35GM131854 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 2019 to 2026
$3.3M
Succinate Dehydrogenase: Biogenesis and Role in DiseaseR01GM110755 · NIGMS · UNIVERSITY OF UTAH · PI WINGE, DENNIS R. · 2014 to 2021
$2.3M
Advancing Multiplexed Isobaric Tag-based Strategies for Proteome ProfilingR01GM132129 · NIGMS · HARVARD MEDICAL SCHOOL · PI PAULO, JOAO A · 2019 to 2023
$1.7M
An Interdisciplinary Approach to Stress-Induced Mitochondrial Quality ControlR01GM115129 · NIGMS · UNIVERSITY OF UTAH · PI HILL, CHRISTOPHER P., RUTTER, JARED P · 2015 to 2018
$1.5M
Msp1/ATAD1: mitochondrial and peroxisomal protein sortingR01GM115174 · NIGMS · UNIVERSITY OF UTAH · PI RUTTER, JARED P · 2015 to 2018
$1.0M
Agilent 6550 QTOF system for U of UtahS10OD016232 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2013 to 2013
$578k
Q-ToF Mass Spectrometer for the University of Utah MS and Proteomics CoreS10OD018210 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2015 to 2015
$530k
Howard Hughes Medical InstituteNCI NIH HHS R35 CA220449NCI NIH HHS R35CA22044901NHLBI NIH HHS T32 HL007576NIA NIH HHS R21 AG063077NICHD NIH HHS F32 HD096786NIDDK NIH HHS R01 DK107397NIDDK NIH HHS T32DK11096601NIDDK NIH HHS U54 DK110858NIGMS NIH HHS GM97645NIGMS NIH HHS R01 GM067945NIGMS NIH HHS R01 GM110755NIGMS NIH HHS R01 GM115129NIGMS NIH HHS R01 GM115174NIGMS NIH HHS R01 GM132129NIGMS NIH HHS R35 GM131854NIH HHS S10 OD016232NIH HHS S10 OD018210NIH HHS S10 OD021505
6 · The paper itself

Abstract

Cells harbor two systems for fatty acid synthesis, one in the cytoplasm (catalyzed by fatty acid synthase, FASN) and one in the mitochondria (mtFAS). In contrast to FASN, mtFAS is poorly characterized, especially in higher eukaryotes, with the major product(s), metabolic roles, and cellular function(s) being essentially unknown. Here we show that hypomorphic mtFAS mutant mouse skeletal myoblast cell lines display a severe loss of electron transport chain (ETC) complexes and exhibit compensatory metabolic activities including reductive carboxylation. This effect on ETC complexes appears to be independent of protein lipoylation, the best characterized function of mtFAS, as mutants lacking lipoylation have an intact ETC. Finally, mtFAS impairment blocks the differentiation of skeletal myoblasts in vitro. Together, these data suggest that ETC activity in mammals is profoundly controlled by mtFAS function, thereby connecting anabolic fatty acid synthesis with the oxidation of carbon fuels.

Indexed as

AnimalsCell DifferentiationCell LineElectron Transport Chain Complex ProteinsFatty AcidsHEK293 CellsHumansLipoylationMiceMitochondriaMyoblastsOxidation-ReductionElectron Transport Chain Complex ProteinsFatty Acidsbiochemistrychemical biologyelectron transport chainfatty acid synthesismetabolismmitochondriamousemyoblastTCA cycle

Identifiers

PMID32804083
PMCPMC7470841
OpenAlexW3049404831

What OpenQuestion holds

Textmetadata
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.