Evidence map›Paper›PMID 39752519›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Endonuclease G promotes hepatic mitochondrial respiration by selectively increasing mitochondrial tRNA

Xihui Xu, Rozhin Penjweini, Lóránt Székvölgyi, Zsolt Karányi, Anne-Marie Heckel, Devikala Gurusamy, Dóra Varga, Shutong Yang, Alexandra L Brown, Wenqi Cui and 15 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Endonuclease G promotes hepatic mitochondrial respiration by selectively increasing mitochondrial tRNAProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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

25 authors.

Xihui XuLaboratory of Obesity and Aging Research, Cardiovascular Branch, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.
Rozhin PenjweiniLaboratory of Advanced Microscopy and Biophotonics, Biochemistry and Biophysics Center, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.ORCID 0009-0001-6407-5859
Lóránt SzékvölgyiMomentum Genome Architecture and Recombination Research Group, Department of Molecular and Nanopharmaceutics, Faculty of Pharmacy, University of Debrecen, Debrecen 4032, Hungary.ORCID 0000-0002-7529-0319
Zsolt KarányiMomentum Genome Architecture and Recombination Research Group, Department of Molecular and Nanopharmaceutics, Faculty of Pharmacy, University of Debrecen, Debrecen 4032, Hungary.
Anne-Marie HeckelUMR 7156 Génétique Moléculaire, Génomique, Microbiologie, Strasbourg University-CNRS, Strasbourg 67000, France.
Devikala GurusamyLaboratory of Obesity and Aging Research, Cardiovascular Branch, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.
Dóra VargaMomentum Genome Architecture and Recombination Research Group, Department of Molecular and Nanopharmaceutics, Faculty of Pharmacy, University of Debrecen, Debrecen 4032, Hungary.ORCID 0009-0005-8999-1246
Shutong YangLaboratory of Obesity and Aging Research, Cardiovascular Branch, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.
Alexandra L BrownLaboratory of Obesity and Aging Research, Cardiovascular Branch, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.ORCID 0009-0007-2787-4225
Wenqi CuiLiver and Energy Metabolism Section, Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD 20892.
Jinsung ParkLaboratory of Obesity and Aging Research, Cardiovascular Branch, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.ORCID 0000-0002-1422-4780
Dénes NagyMomentum Genome Architecture and Recombination Research Group, Department of Molecular and Nanopharmaceutics, Faculty of Pharmacy, University of Debrecen, Debrecen 4032, Hungary.
Maren C PodszunLiver and Energy Metabolism Section, Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD 20892.
Sarah YangDNA Sequencing and Genomics Core Facility, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.
Komudi SinghBioinformatics Core Facility, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.
Stephen P AshcroftSchool of Sport, Exercise and Rehabilitation Sciences, University of Birmingham, Birmingham B152TT, United Kingdom.
Jeonghan KimDepartment of Biochemistry, College of Medicine, The Catholic University of Korea, Seoul 06591, South Korea.ORCID 0000-0003-1695-9630
Myung K KimLaboratory of Obesity and Aging Research, Cardiovascular Branch, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.
Ivan TarassovUMR 7156 Génétique Moléculaire, Génomique, Microbiologie, Strasbourg University-CNRS, Strasbourg 67000, France.ORCID 0000-0001-8763-6703
Jun ZhuDNA Sequencing and Genomics Core Facility, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.
Andrew PhilpCentre for Healthy Ageing, Centenary Institute, Royal Prince Alfred Hospital, Sydney, NSW 2050, Australia.
Yaron RotmanLiver and Energy Metabolism Section, Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD 20892.ORCID 0000-0002-7549-8216
Jay R KnutsonLaboratory of Advanced Microscopy and Biophotonics, Biochemistry and Biophysics Center, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.ORCID 0000-0001-9990-1738
Nina EntelisUMR 7156 Génétique Moléculaire, Génomique, Microbiologie, Strasbourg University-CNRS, Strasbourg 67000, France.ORCID 0000-0002-7915-5528
Jay H ChungLaboratory of Obesity and Aging Research, Cardiovascular Branch, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892.ORCID 0000-0002-2459-526X

Funding

HHS | NIH (NIH) HL006119-12
6 · The paper itself

Abstract

Mitochondrial endonuclease G (EndoG) contributes to chromosomal degradation when it is released from mitochondria during apoptosis. It is presumed to also have a mitochondrial function because EndoG deficiency causes mitochondrial dysfunction. However, the mechanism by which EndoG regulates mitochondrial function is not known. Fat accumulation in metabolic dysfunction-associated steatotic liver disease (MASLD), which is more common in men, is caused in part by mitochondrial dysfunction. EndoG expression is reduced in MASLD liver, and EndoG deficiency causes MASLD in an obesity-independent manner but only in males. EndoG promotes mitochondrial respiration by resolving mitochondrial tRNA/DNA hybrids formed during mtDNA transcription by recruiting RNA helicase DHX30 to unwind them. EndoG also cleaves off the 3'-end of the H-strand transcript that can prevent mt-tRNA

Indexed as

EndodeoxyribonucleasesMitochondria, LiverAnimalsCell RespirationDEAD-box RNA HelicasesDNA, MitochondrialFatty LiverHumansLiverMaleMiceMice, KnockoutMitochondriaOxygen ConsumptionDEAD-box RNA HelicasesDNA, MitochondrialEndodeoxyribonucleasesendonuclease Gendonuclease GMASLDmitochondriatRNA

Identifiers

PMID39752519
PMCPMC11725929

What OpenQuestion holds

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LicenceCC BY
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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.