# Evolutionary engineering and molecular characterization of an antimycin A-resistant Saccharomyces cerevisiae strain: the key role of pleiotropic drug resistance (PDR1)

**Authors:** Alican Topaloğlu, Can Holyavkin, Ömer Esen, Ogün Morkoç, Karl Persson, Cecilia Geijer, Zeynep Petek Çakar

PMC · DOI: 10.1093/femsyr/foaf062 · FEMS Yeast Research · 2025-10-17

## TL;DR

Scientists evolved a yeast strain resistant to an antifungal drug and found a key gene involved in this resistance.

## Contribution

First evolutionary engineering of an antimycin A-resistant yeast strain and identification of PDR1's role in resistance.

## Key findings

- A Pdr1p.M732R mutation alone confers antimycin A resistance in S. cerevisiae.
- Transcriptomic changes in PDR, transport, trafficking, and autophagy pathways were observed in the resistant strain.
- Evolved resistance was achieved without prior mutagenesis through gradual stress exposure.

## Abstract

Antimycin A, an antifungal agent that inhibits mitochondrial respiration, provides a useful model for studying resistance mechanisms. Antifungal resistance is an escalating clinical concern with limited treatment options available. To understand the molecular mechanisms of antimycin A resistance, a genetically stable, antimycin A-resistant Saccharomyces cerevisiae strain was successfully developed for the first time through an evolutionary engineering strategy, based on long-term systematic application of gradually increasing antimycin A stress in repetitive batch cultures without prior chemical mutagenesis. Comparative whole genome resequencing analysis of the evolved strain ant905-9 revealed two missense mutations in PDR1 and PRP8 genes involved in pleiotropic drug resistance and RNA splicing, respectively. Using CRISPR/Cas9 genome editing tools, the identified mutations were introduced individually and together into the reference strain, and it was confirmed that the Pdr1p.M732R mutation alone confers antimycin A-resistance in S. cerevisiae. Comparative transcriptomic analysis of the reverse-engineered Pdr1p.M732R strain showed alterations in PDR (pleiotropic drug resistance), transmembrane transport, vesicular trafficking, and autophagy pathways. Our results highlight the potential key role of PDR1 in antifungal drug resistance. This study provides new insights into mitochondrial drug resistance and the adaptive potential of yeast under respiratory stress.

Evolutionary engineering of an antimycin A-resistant Saccharomyces cerevisiae strain, comparative omic analyses, and reverse engineering using CRISPR/Cas9 revealed the importance of PDR1 gene in antifungal drug resistance.

## Linked entities

- **Genes:** pdr-1 (E3 ubiquitin-protein ligase parkin;RBR-type E3 ubiquitin transferase;Ubiquitin-like domain-containing protein) [NCBI Gene 176816], DHX16 (DEAH-box helicase 16) [NCBI Gene 8449]
- **Chemicals:** antimycin A (PubChem CID 14957)
- **Species:** Saccharomyces cerevisiae (taxon 4932)

## Full-text entities

- **Genes:** PDR1 (drug-responsive transcription factor PDR1) [NCBI Gene 852871] {aka AMY1, ANT1, BOR2, CYH3, NRA2, SMR2}, PRP8 (U4/U6-U5 snRNP complex subunit PRP8) [NCBI Gene 856570] {aka DBF3, DNA39, RNA8, SLT21, USA2}
- **Chemicals:** Antimycin A (MESH:D000968)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]
- **Mutations:** p.M732R

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12570882/full.md

## References

87 references — full list in the complete paper: https://tomesphere.com/paper/PMC12570882/full.md

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Source: https://tomesphere.com/paper/PMC12570882