Evidence map›Paper›PMID 35220898›Full record

ArticleAutophagy2022

Autophagy deficiency abolishes liver mitochondrial DNA segregation.

Katiane Tostes, Angélica C Dos Santos, Lindomar O Alves, Luiz R G Bechara, Rachel Marascalchi, Carolina H Macabelli, Mateus P Grejo, William T Festuccia, Roberta A Gottlieb, Julio C B Ferreira and 1 more

Open access · greenAbstract read
In one paragraph

Article in Autophagy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 20 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

11 authors at 3 institutions in 2 countries.

Katiane TostesDepartamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, Brazil.ORCID 0000-0002-8312-9269
Angélica C Dos SantosDepartamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, Brazil.ORCID 0000-0001-8156-4059
Lindomar O AlvesDepartamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, Brazil.ORCID 0000-0001-6450-0555
Luiz R G BecharaDepartment of Anatomy, Institute of Biomedical Sciences, University of Sao Paulo, São Paulo, Brazil.ORCID 0000-0002-1642-1008
Rachel MarascalchiDepartamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, Brazil.ORCID 0000-0003-2114-8226
Carolina H MacabelliDepartamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, Brazil.ORCID 0000-0001-5865-9156
Mateus P GrejoDepartamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, Brazil.ORCID 0000-0001-8558-0515
William T FestucciaDepartment of Physiology and Biophysics, Institute of Biomedical Sciences, University of Sao Paulo, São Paulo, Brazil.ORCID 0000-0003-4769-0806
Roberta A GottliebDepartment of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, CA, USA.ORCID 0000-0002-1432-006X
Julio C B FerreiraDepartment of Anatomy, Institute of Biomedical Sciences, University of Sao Paulo, São Paulo, Brazil.ORCID 0000-0003-2694-239X
Marcos R ChiarattiDepartamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, Brazil.ORCID 0000-0001-8805-9469
Universidade Federal de São Carlos · BRUniversidade de São Paulo · BRCedars-Sinai Medical Center · US

Funding

Regulation of the Dynamic Proteome after Ischemic InjuryR01HL144509 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI GOTTLIEB, ROBERTA A., VAN EYK, JENNIFER E · 2019 to 2022
$2.9M
Mitochondrial Turnover in the Human HeartR01HL132075 · NHLBI · CEDARS-SINAI MEDICAL CENTER · PI GOTTLIEB, ROBERTA A., VAN EYK, JENNIFER E · 2017 to 2020
$2.1M
NHLBI NIH HHS R01 HL132075NHLBI NIH HHS R01 HL144509
6 · The paper itself

Abstract

Mutations in the mitochondrial genome (mtDNA) are ubiquitous in humans and can lead to a broad spectrum of disorders. However, due to the presence of multiple mtDNA molecules in the cell, co-existence of mutant and wild-type mtDNAs (termed heteroplasmy) can mask disease phenotype unless a threshold of mutant molecules is reached. Importantly, the mutant mtDNA level can change across lifespan as mtDNA segregates in an allele- and cell-specific fashion, potentially leading to disease. Segregation of mtDNA is mainly evident in hepatic cells, resulting in an age-dependent increase of mtDNA variants, including non-synonymous potentially deleterious mutations. Here we modeled mtDNA segregation using a well-established heteroplasmic mouse line with mtDNA of NZB/BINJ and C57BL/6N origin on a C57BL/6N nuclear background. This mouse line showed a pronounced age-dependent NZB mtDNA accumulation in the liver, thus leading to enhanced respiration capacity per mtDNA molecule. Remarkably, liver-specific

Indexed as

MitophagyNADP TranshydrogenasesAdenosine TriphosphateAdultAnimalsApolipoproteinsApolipoproteins BAutophagyCarbon DioxideCarbonyl Cyanide p-TrifluoromethoxyphenylhydrazoneCytochromes bDNA-Binding ProteinsDNA, MitochondrialElectron Transport Complex IIIElectron Transport Complex IVHumansAdenosine TriphosphateApolipoproteinsApolipoproteins BCarbon DioxideCarbonyl Cyanide p-TrifluoromethoxyphenylhydrazoneCytochromes bDNA-Binding ProteinsDNA, MitochondrialElectron Transport Complex IIIElectron Transport Complex IVIronMicrotubule-Associated ProteinsMitochondrial ProteinsNABP2 protein, humanNADNADP TranshydrogenasesPeptidylprolyl IsomerasePPAR alphaProtein KinasesProto-Oncogene Proteins c-bcl-2Ribosomal ProteinsSequestosome-1 ProteinSuccinate DehydrogenaseSulfurTranscription FactorsUbiquinoneUbiquitin-Protein LigasesUbiquitinsAtg7heteroplasmymitochondriamitophagyNZBparkin

Identifiers

PMID35220898
PMCPMC9542960
OpenAlexW4214602952

What OpenQuestion holds

Textmetadata
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.