GenesMolecular BiologyPeer-reviewed journal article
A primer genetic toolkit for exploring mitochondrial biology and disease using zebrafish
Ankit SabharwaliD, Jarryd M. CampbelliD, Tanya L. Schwab, Zachary WareJoncasiD, Mark D. WishmaniD, Hirotaka AtaiD, Wiebin Liu, Noriko IchinoiD, Danielle E. Hunter, Jake D. Bergren, Mark D. UrbaniD, Rhianna M. UrbaniD, Shannon R. HolmbergiD, Bibekananda KariD, Alex Richard CookiD, Yonghe DingiD, Xiaolei XuiD, Karl J. ClarkiD, Stephen Carl EkkeriD
Abstract
Mitochondria are a dynamic eukaryotic innovation that play diverse roles in biology and disease. The mitochondrial genome is remarkably conserved in all vertebrates, encoding the same 37 gene set and overall genomic structure ranging from 16,596 base pairs (bp) in the teleost zebrafish (Danio rerio) to 16,569 bp in humans. Mitochondrial disorders are amongst the most prevalent inherited diseases affecting roughly 1 in every 5000 individuals. Currently, few effective treatments exist for those with mitochondrial ailments, representing a major unmet patient need. Mitochondrial dysfunction is also implicated to be a common component of a wide variety of other human illnesses ranging from neurodegenerative disorders like Huntingtons disease and Parkinsons disease to autoimmune illnesses such as multiple sclerosis and rheumatoid arthritis. The electron transport chain (ETC) component of mitochondria is critical for mitochondrial biology and defects can lead to many mitochondrial disease symptoms. Here we present a publicly available collection of genetic mutants created in highly conserved, nuclear-encoded mitochondrial genes in Danio rerio. The zebrafish system represents a potentially powerful new opportunity for the study of mitochondrial biology and disease due to the large number of orthologous genes shared with humans and the many advanced features of this model system from genetics to imaging. This collection includes 22 mutant lines in 18 different genes created by locus-specific gene editing to induce frameshift or splice acceptor mutations leading to predicted protein truncation during translation. Also included are 6 lines created by the random insertion of the gene-breaking transposon (GBT) protein trap cassette. All of these targeted mutant alleles truncate conserved domains of genes critical to the proper function of the ETC or genes that have been implicated in human mitochondrial disease. This collection is designed to accelerate the use of zebrafish to study of many different aspects of mitochondrial function with the goal of widening our understanding of their role in biology and human disease.
- Citations
- 15
- FWCI
- 1.20
- Field percentile
- top 26%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Systematic Engineering of Loss-of-Function Alleles in the Zebrafish Mitochondrial Proteome
Ankit Sabharwal, Md Roushan Ali, … Stephen Carl Ekker·bioRxiv·Sep 17, 2026
- Transcriptome analysis of atad3-null zebrafish embryos elucidates possible disease mechanisms
Shlomit Ezer, Nathan Ronin, … Tamar Harel·Orphanet Journal of Rare DiseasesPeer-reviewed·Apr 15, 2025
- Engineering targeted deletions in the mitochondrial genome
Jarryd M. Campbell, Ester Perales‐Clemente, … Stephen Carl Ekker·bioRxiv·Mar 22, 2018
- Profiling subcellular localization of nuclear-encoded mitochondrial gene products in zebrafish
Barbara Uszczyńska-Ratajczak, Sreedevi Sugunan, … Agnieszka Chacińska·Life Science AlliancePeer-reviewed·Oct 25, 2022
- Strategies for the modulation of mitochondrial metabolism and activity in the treatment of neurodegenerative diseases: A systematic review and meta-analysis.
Piedad Valverde-Guillén, Pedro Seoane, … Manuel Bernal-Quirós·bioRxiv·Mar 11, 2026
- A Genetic Model Therapy Proposes a Critical Role for Liver Dysfunction in Mitochondrial Biology and Disease
Ankit Sabharwal, Mark D. Wishman, … Stephen Carl Ekker·eLifePeer-reviewed·Nov 21, 2022