Evidence map›Paper›PMID 38643274›Full record

ArticleCell death & disease2024

Zebrafish polg2 knock-out recapitulates human POLG-disorders; implications for drug treatment.

Raquel Brañas Casas, Alessandro Zuppardo, Giovanni Risato, Alberto Dinarello, Rudy Celeghin, Camilla Fontana, Eleonora Grelloni, Alexandru Ionut Gilea, Carlo Viscomi, Andrea Rasola and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. 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

16 authors at 3 institutions in 3 countries.

Raquel Brañas CasasDepartment of Biology, University of Padova, Padova, 35131, Italy.ORCID 0000-0002-0908-4330
Alessandro ZuppardoDepartment of Biomedical Sciences, University of Padova, Padova, 35131, Italy.
Giovanni RisatoDepartment of Biology, University of Padova, Padova, 35131, Italy.ORCID 0000-0003-0651-7409
Alberto DinarelloDepartment of Biology, University of Padova, Padova, 35131, Italy.
Rudy CeleghinDepartment of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padova, Padova, 35128, Italy.
Camilla FontanaDepartment of Biology, University of Padova, Padova, 35131, Italy.
Eleonora GrelloniDepartment of Biology, University of Padova, Padova, 35131, Italy.
Alexandru Ionut GileaDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, 43124, Italy.
Carlo ViscomiDepartment of Biomedical Sciences, University of Padova, Padova, 35131, Italy.ORCID 0000-0001-6050-0566
Andrea RasolaDepartment of Biomedical Sciences, University of Padova, Padova, 35131, Italy.ORCID 0000-0003-4522-3008
Luisa Dalla ValleDepartment of Biology, University of Padova, Padova, 35131, Italy.ORCID 0000-0001-8097-6369
Tiziana LodiDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, 43124, Italy.ORCID 0000-0002-7294-8971
Enrico BaruffiniDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, 43124, Italy.ORCID 0000-0002-8280-7849
Nicola FacchinelloNeuroscience Institute, Italian Research Council (CNR), 35131, Padova, Italy. nicola.facchinello@cnr.it.
Francesco ArgentonDepartment of Biology, University of Padova, Padova, 35131, Italy. francesco.argenton@unipd.it.ORCID 0000-0002-0803-8236
Natascia TisoDepartment of Biology, University of Padova, Padova, 35131, Italy. natascia.tiso@unipd.it.ORCID 0000-0002-5444-9853
University of Padua · ITUniversity of Parma · ITNeuroscience Institute · IT

Funding

AFM-Téléthon (French Muscular Dystrophy Association) 18572AFM-Téléthon (French Muscular Dystrophy Association) 23706Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) IG-2017-19928Fondazione Telethon (Telethon Foundation) GGP19287Fondazione Telethon (Telethon Foundation) GGP19287AFondazione Telethon (Telethon Foundation) GGP20013Ministero dell'Istruzione, dell'Università e della Ricerca (Ministry of Education, University and Research) PNRR M4C2 CN00000041
6 · The paper itself

Abstract

The human mitochondrial DNA polymerase gamma is a holoenzyme, involved in mitochondrial DNA (mtDNA) replication and maintenance, composed of a catalytic subunit (POLG) and a dimeric accessory subunit (POLG2) conferring processivity. Mutations in POLG or POLG2 cause POLG-related diseases in humans, leading to a subset of Mendelian-inherited mitochondrial disorders characterized by mtDNA depletion (MDD) or accumulation of multiple deletions, presenting multi-organ defects and often leading to premature death at a young age. Considering the paucity of POLG2 models, we have generated a stable zebrafish polg2 mutant line (polg2

Indexed as

DNA-Directed DNA PolymeraseMitochondrial DiseasesAnimalsDNA, MitochondrialDNA Polymerase gammaHumansMitochondriaMutationZebrafishDNA-Directed DNA PolymeraseDNA, MitochondrialDNA Polymerase gammaPOLG protein, human

Identifiers

PMID38643274
PMCPMC11032366
OpenAlexW4394976777

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.