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Humanized yeast to model human biology, disease and evolution.
- Source :
-
Disease models & mechanisms [Dis Model Mech] 2022 Jun 01; Vol. 15 (6). Date of Electronic Publication: 2022 Jun 06. - Publication Year :
- 2022
-
Abstract
- For decades, budding yeast, a single-cellular eukaryote, has provided remarkable insights into human biology. Yeast and humans share several thousand genes despite morphological and cellular differences and over a billion years of separate evolution. These genes encode critical cellular processes, the failure of which in humans results in disease. Although recent developments in genome engineering of mammalian cells permit genetic assays in human cell lines, there is still a need to develop biological reagents to study human disease variants in a high-throughput manner. Many protein-coding human genes can successfully substitute for their yeast equivalents and sustain yeast growth, thus opening up doors for developing direct assays of human gene function in a tractable system referred to as 'humanized yeast'. Humanized yeast permits the discovery of new human biology by measuring human protein activity in a simplified organismal context. This Review summarizes recent developments showing how humanized yeast can directly assay human gene function and explore variant effects at scale. Thus, by extending the 'awesome power of yeast genetics' to study human biology, humanizing yeast reinforces the high relevance of evolutionarily distant model organisms to explore human gene evolution, function and disease.<br />Competing Interests: Competing interests The authors declare no competing or financial interests.<br /> (© 2022. Published by The Company of Biologists Ltd.)
- Subjects :
- Humans
Phenotype
Proteins
Models, Biological
Yeasts genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1754-8411
- Volume :
- 15
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Disease models & mechanisms
- Publication Type :
- Academic Journal
- Accession number :
- 35661208
- Full Text :
- https://doi.org/10.1242/dmm.049309