# Yeast as a Model for Human Disease

**Authors:** Bartłomiej Zieniuk, Katarzyna Wierzchowska, Karina Jasińska, Joanna Kobus, Aleksandra Piotrowicz, Şuheda Uğur, Agata Fabiszewska

PMC · DOI: 10.3390/ijms27041632 · International Journal of Molecular Sciences · 2026-02-07

## TL;DR

Yeast species are used as models to study human diseases due to their genetic simplicity and shared biological pathways with humans.

## Contribution

The paper reviews the use of various yeast species in modeling human diseases and highlights their role in biomedical research and drug discovery.

## Key findings

- Yeast models have been used to study neurodegenerative diseases like Alzheimer’s and Huntington’s.
- Humanized yeast models allow for the expression and analysis of human genes and proteins.
- Yeast is increasingly important in cancer research and personalized medicine.

## Abstract

Yeasts, especially the conventional species Saccharomyces cerevisiae and Schizosaccharomyces pombe, as well as some unconventional species such as Pichia pastoris, Kluyveromyces marxianus and Yarrowia lipolytica, have become fundamental model organisms for understanding the molecular mechanisms underlying human diseases. Their eukaryotic cell organization, genetic simplicity, and strong conservation of essential biological pathways make them indispensable in biomedical research. This review provides a comprehensive overview of the role of different yeast species in modeling human disorders, highlighting historical milestones and groundbreaking discoveries that have shaped current knowledge. The article discusses the applications of yeast models in studying neurodegenerative diseases such as Alzheimer’s and Huntington’s, as well as metabolic diseases, infectious diseases and mitochondrial disorders, and their growing importance in cancer research and drug discovery. Special attention is given to humanized yeast models, which enable the expression and functional analysis of human genes and the heterologous synthesis of human proteins within yeast cells. Finally, the paper addresses the limitations and challenges of yeast as a model system while outlining future directions and emphasizing the organism’s continued relevance in personalized medicine and functional genomics.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)
- **Species:** Saccharomyces cerevisiae (taxon 4932), Schizosaccharomyces pombe (taxon 4896), Kluyveromyces marxianus (taxon 4911), Yarrowia lipolytica (taxon 4952)

## Full-text entities

- **Genes:** HER2 (glutamyl-tRNA(Gln) amidotransferase subunit HER2) [NCBI Gene 855338] {aka GEP6, QRS1, RRG6}, ASA1 (Asa1p) [NCBI Gene 856200], HIF1 (Hif1p) [NCBI Gene 850638], PDR1 (drug-responsive transcription factor PDR1) [NCBI Gene 852871] {aka AMY1, ANT1, BOR2, CYH3, NRA2, SMR2}, YAP3 (Yap3p) [NCBI Gene 856377], COX1 (cytochrome c oxidase subunit 1) [NCBI Gene 854598] {aka OXI3}, PDR5 (ATP-binding cassette multidrug transporter PDR5) [NCBI Gene 854324] {aka LEM1, STS1, YDR1}, VPS13 (membrane morphogenesis protein VPS13) [NCBI Gene 850619] {aka SOI1, VPT2, YME3}, ACT1 (actin) [NCBI Gene 850504] {aka ABY1, END7}, CLN3 (cyclin CLN3) [NCBI Gene 851191] {aka DAF1, FUN10, WHI1}, ATM (Serine/Threonine-kinase ATM-like protein) [NCBI Gene 823975] {aka ARABIDOPSIS THALIANA ATAXIA-TELANGIECTASIA MUTATED, ATATM, PIG1, ataxia-telangiectasia mutated, pcd in male gametogenesis 1}, TTI1 (Tti1p) [NCBI Gene 853834], TEL1 (DNA-binding protein kinase TEL1) [NCBI Gene 852190], RAD51 (recombinase RAD51) [NCBI Gene 856831] {aka MUT5}, UBI4 (ubiquitin) [NCBI Gene 850620] {aka SCD2, UB14}, PDR3 (drug-responsive transcription factor PDR3) [NCBI Gene 852278] {aka AMY2, TPE2}, RIM11 (serine/threonine protein kinase RIM11) [NCBI Gene 855170] {aka GSK3, MDS1}, MKC7 (aspartyl protease) [NCBI Gene 851722] {aka YPS2}, TOR2 (phosphatidylinositol kinase-related protein kinase TOR2) [NCBI Gene 853632] {aka DRR2}, ATP6 (F1F0 ATP synthase subunit a) [NCBI Gene 854601] {aka OLI2, OLI4, PHO1}, URE2 (glutathione peroxidase) [NCBI Gene 855492], YHC3 (amino acid transporter YHC3) [NCBI Gene 853387] {aka BTN1}, SNQ2 (ATP-binding cassette transporter SNQ2) [NCBI Gene 851574], RAD55 (putative DNA-dependent ATPase RAD55) [NCBI Gene 851648], RAD52 (recombinase RAD52) [NCBI Gene 854976], ALG3 (dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichol alpha-1,3-mannosyltransferase) [NCBI Gene 852196] {aka RHK1}, MHR1 (mitochondrial 54S ribosomal protein mL67 MHR1) [NCBI Gene 851890] {aka XTC1, mL67}, PHO85 (cyclin-dependent serine/threonine-protein kinase PHO85) [NCBI Gene 856076] {aka LDB15}, OCH1 (initiation-specific alpha-1,6-mannosyltransferase) [NCBI Gene 852845] {aka LDB12, NGD29}, SUP35 (translation termination factor GTPase eRF3) [NCBI Gene 851752] {aka GST1, PNM2, SAL3, SUF12, SUP2, SUP36}
- **Diseases:** neurological disorders (MESH:D009461), genetic disorders (MESH:D030342), Metabolic Disorders (MESH:D008659), MD (MESH:C535955), immunodeficiency disorder (MESH:D000081207), Friedreich's Ataxia (MESH:D005621), hypoxia (MESH:D000860), Respiratory-deficient (MESH:D012131), centronuclear myopathies (MESH:D020914), Niemann-Pick disease (MESH:D009542), prion-like disorders (MESH:D017096), obesity (MESH:D009765), complex I-linked disorders (MESH:C537475), difficulties in learning (MESH:D007859), WAS (MESH:D014923), AD (MESH:D000544), neurotoxic (MESH:D020258), HD (MESH:D006816), diabetes (MESH:D003920), Cancer (MESH:D009369), chromosomal abnormalities (MESH:D002869), Lysosomal Storage Disorders (MESH:D016464), Neurodegenerative (MESH:D019636), injury to (MESH:D014947), inflammation (MESH:D007249), hereditary cancer syndromes (MESH:D009386), PD (MESH:D010300), multidrug (MESH:D018088), muscle stiffness (MESH:D019042), TDP-43 (MESH:D057177), Mitochondrial diseases (MESH:D028361), immune dysregulation (OMIM:614878), Hereditary Spastic Paraplegia (MESH:D015419), FTD (MESH:D057180), MELAS- (MESH:D017241), Neuromuscular Disease Proteinopathies (MESH:D009468), Leigh syndrome (MESH:D007888), intestinal (MESH:D007410), CIN (MESH:D043171), Lipid (MESH:D011017), Cognitive decline (MESH:D003072), Haploinsufficiency (MESH:C565160), aneuploidy (MESH:D000782), MERRF-like syndromes (MESH:D017243), memory impairment (MESH:D008569), Infectious Disease (MESH:D003141), Charcot-Marie-Tooth disease (MESH:D002607), neuronal injury (MESH:D009410), IBD (MESH:D015212), BRCA-deficient cancers (MESH:D001943), dementia (MESH:D003704), amyloid (MESH:C000718787), delayed movements (MESH:D020820), 17 (OMIM:615607), infection (MESH:D007239), thrombocytopenia (MESH:D013921), Neurodegenerative tauopathies (MESH:D024801), cytotoxic (MESH:D064420), proteinopathies (MESH:D057165), SL (OMIM:146820)
- **Chemicals:** alkanes (MESH:D000473), alkaloids (MESH:D000470), noscapine (MESH:D009665), cholesterol (MESH:D002784), leucine (MESH:D007930), methotrexate (MESH:D008727), bortezomib (MESH:D000069286), paclitaxel (MESH:D017239), nitrogen (MESH:D009584), beta-1,3-glucans (MESH:C033363), trastuzumab (MESH:D000068878), carbon (MESH:D002244), rapamycin (MESH:D020123), polyacrylamide (MESH:C016679), gold (MESH:D006046), oxygen (MESH:D010100), NADH (MESH:D009243), cyanide (MESH:D003486), glucose (MESH:D005947), SCFAs (MESH:D005232), beta-glucans (MESH:D047071), ROS (MESH:D017382), polyQ (MESH:C097188), ATP (MESH:D000255), LPS (MESH:D008070), Lipid (MESH:D008055), tungsten (MESH:D014414), Dimebon (MESH:C010119), ergosterol (MESH:D004875), amino acids (MESH:D000596), arginine (MESH:D001120), H2O2 (MESH:D006861), cisplatin (MESH:D002945), alpha-mannan (-), caffeine (MESH:D002110), glycerol (MESH:D005990)
- **Species:** Kluyveromyces marxianus (species) [taxon 4911], Komagataella pastoris (species) [taxon 4922], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Ogataea angusta (species) [taxon 870730], Nakaseomyces glabratus (species) [taxon 5478], Mus musculus (house mouse, species) [taxon 10090], Yarrowia lipolytica (species) [taxon 4952], Caenorhabditis elegans (species) [taxon 6239], S. boulardii [taxon 252598], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Schizosaccharomyces pombe (fission yeast, species) [taxon 4896], Candida albicans (species) [taxon 5476], Escherichia coli (E. coli, species) [taxon 562], Lathyrus oleraceus (garden pea, species) [taxon 3888], gut metagenome (species) [taxon 749906], Drosophila melanogaster (fruit fly, species) [taxon 7227], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Kluyveromyces lactis (species) [taxon 28985], Lachancea cidri (species) [taxon 29831], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Hepacivirus P (species) [taxon 2202225], Danio rerio (leopard danio, species) [taxon 7955]
- **Mutations:** P301L
- **Cell lines:** CHO — Cricetulus griseus (Chinese hamster), Spontaneously immortalized cell line (CVCL_0213)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941056/full.md

## References

226 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941056/full.md

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Source: https://tomesphere.com/paper/PMC12941056