Evidence map›Paper›PMID 35683014›Full record

ArticleInternational journal of molecular sciences2022

The Consequences of Mitochondrial T10432C Mutation in Cika Cattle: A "Potential" Model for Leber's Hereditary Optic Neuropathy.

Dinko Novosel, Vladimir Brajković, Mojca Simčič, Minja Zorc, Tanja Svara, Karmen Branovic Cakanic, Andreja Jungić, Betka Logar, Vlatka Cubric-Curik, Peter Dovc and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Piperine alleviates retinal ischemic injury by mediating the APE1 signaling.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    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

11 authors at 4 institutions in 2 countries.

Dinko NovoselDepartment of Pathology, Croatian Veterinary Institute, 10000 Zagreb, Croatia.ORCID 0000-0003-2602-8696
Vladimir BrajkovićDepartment of Animal Science, Faculty of Agriculture, University of Zagreb, 10000 Zagreb, Croatia.
Mojca SimčičDepartment of Animal Science, Biotechnical Faculty, University of Ljubljana, 1000 Ljubljana, Slovenia.
Minja ZorcDepartment of Animal Science, Biotechnical Faculty, University of Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0003-3330-7909
Tanja SvaraInstitute of Pathology, Wild Animals, Fish and Bees, Veterinary Faculty, University of Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0001-5469-9273
Karmen Branovic CakanicDepartment of Pathology, Croatian Veterinary Institute, 10000 Zagreb, Croatia.
Andreja JungićDepartment of Virology, Croatian Veterinary Institute, 10000 Zagreb, Croatia.
Betka LogarAgricultural Institute of Slovenia, 1000 Ljubljana, Slovenia.
Vlatka Cubric-CurikDepartment of Animal Science, Faculty of Agriculture, University of Zagreb, 10000 Zagreb, Croatia.
Peter DovcDepartment of Animal Science, Biotechnical Faculty, University of Ljubljana, 1000 Ljubljana, Slovenia.ORCID 0000-0002-7418-0054
Ino CurikDepartment of Animal Science, Faculty of Agriculture, University of Zagreb, 10000 Zagreb, Croatia.ORCID 0000-0001-7090-1654
University of Ljubljana · SIUniversity of Zagreb · HRCroatian Veterinary Institute · HRAgricultural institute of Slovenia · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While mitogenome mutations leading to pathological manifestations are rare, more than 200 such mutations have been described in humans. In contrast, pathogenic mitogenome mutations are rare in domestic animals and have not been described at all in cattle. In the small local Slovenian cattle breed Cika, we identified (next-generation sequencing) two cows with the T10432C mitogenome mutation in the ND4L gene, which corresponds to the human T10663C mutation known to cause Leber's hereditary optic neuropathy (LHON). Pedigree analysis revealed that the cows in which the mutation was identified belong to two different maternal lineages with 217 individual cows born between 1997 and 2020. The identified mutation and its maternal inheritance were confirmed by Sanger sequencing across multiple generations, whereas no single analysis revealed evidence of heteroplasmy. A closer clinical examination of one cow with the T10432C mutation revealed exophthalmos, whereas histopathological examination revealed retinal ablations, subretinal oedema, and haemorrhage. The results of these analyses confirm the presence of mitochondrial mutation T10432C with homoplasmic maternal inheritance as well as clinical and histopathological signs similar to LHON in humans. Live animals with the mutation could be used as a suitable animal model that can improve our understanding of the pathogenesis of LHON and other mitochondriopathies.

Indexed as

Optic Atrophy, Hereditary, LeberAnimalsCattleDNA, MitochondrialFamilyFemaleMutationPedigreeDNA, Mitochondrialanimal modelcattledetrimental mutationsLHONmitogenomeretinal ablation

Identifiers

PMID35683014
PMCPMC9181260
OpenAlexW4281871990

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.