# Model organisms in POLG-related disorders: insights from yeast to multicellular systems

**Authors:** Raquel Brañas Casas, Giovanni Risato, Alessandro Zuppardo, Carlo Viscomi, Francesco Argenton, Mara Doimo, Nicola Facchinello, Natascia Tiso

PMC · DOI: 10.1038/s41419-025-08366-6 · Cell Death & Disease · 2025-12-26

## TL;DR

This review explores how model organisms from yeast to zebrafish help understand POLG-related mitochondrial diseases and develop treatments.

## Contribution

The paper systematically reviews the use of multiple model organisms in studying POLG-related disorders and their therapeutic implications.

## Key findings

- Yeast and worm models have provided foundational insights into POLG function and disease mechanisms.
- Zebrafish is emerging as a valuable model for drug screening due to its optical transparency and genetic tools.
- Mouse models have advanced understanding of systemic effects in mammals with POLG mutations.

## Abstract

Mitochondrial genetic diseases are complex disorders that impair cellular energy production, leading to diverse clinical manifestations across multiple organ systems. These diseases arise from mutations in either mitochondrial DNA or nuclear DNA. Among nuclear DNA-related cases, mutations in POLG and POLG2, which encode subunits of mitochondrial DNA polymerase γ, are particularly significant, causing conditions such as Alpers–Huttenlocher syndrome and progressive external ophthalmoplegia. Model organisms have been instrumental in elucidating POLG-related disease mechanisms and advancing therapeutic strategies. Saccharomyces cerevisiae (budding yeast) provided insights into fundamental mitochondrial functions, while Caenorhabditis elegans (roundworm) helped explore POLG’s roles in multicellular organisms. Drosophila melanogaster (fruit fly) has been pivotal in studying neurological aspects, and Mus musculus (mouse) models contributed to understanding systemic effects in mammals. Recently, Danio rerio (zebrafish) has emerged as a promising vertebrate model for drug screening, due to its optical transparency and genetic tractability. Each model system offers unique advantages, collectively bridging the gap between basic research and clinical applications. This review will examine in vivo models used in POLG disorder research, highlighting their contributions to understanding disease mechanisms and therapeutic advancements.

## Linked entities

- **Genes:** POLG (DNA polymerase gamma, catalytic subunit) [NCBI Gene 5428], POLG2 (DNA polymerase gamma 2, accessory subunit) [NCBI Gene 11232]
- **Diseases:** Alpers–Huttenlocher syndrome (MONDO:0008758), progressive external ophthalmoplegia (MONDO:0005181)
- **Species:** Saccharomyces cerevisiae (taxon 4932), Caenorhabditis elegans (taxon 6239), Drosophila melanogaster (taxon 7227), Mus musculus (taxon 10090), Danio rerio (taxon 7955)

## Full-text entities

- **Diseases:** POLG disorder (OMIM:613662), Mitochondrial genetic diseases (MESH:D028361), external ophthalmoplegia (MESH:D009886), Alpers-Huttenlocher syndrome (MESH:D002549)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Mus musculus (house mouse, species) [taxon 10090], Caenorhabditis elegans (species) [taxon 6239], Danio rerio (leopard danio, species) [taxon 7955], Drosophila melanogaster (fruit fly, species) [taxon 7227]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12847702/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12847702/full.md

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Source: https://tomesphere.com/paper/PMC12847702