Understanding the molecular mechanisms of human diseases: the benefits of fission yeasts
The role of model organisms such as yeasts in life science research is crucial. Although the baker's yeast ( ) is the most popular model among yeasts, the contribution of the fission yeasts ( ) to life science is also indisputable. Since both types of yeasts share several thousands of common or...
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Veröffentlicht in: | Microbial cell 2024-01, Vol.11, p.288-311 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The role of model organisms such as yeasts in life science research is crucial. Although the baker's yeast (
) is the most popular model among yeasts, the contribution of the fission yeasts (
) to life science is also indisputable. Since both types of yeasts share several thousands of common orthologous genes with humans, they provide a simple research platform to investigate many fundamental molecular mechanisms and functions, thereby contributing to the understanding of the background of human diseases. In this review, we would like to highlight the many advantages of fission yeasts over budding yeasts. The usefulness of fission yeasts in virus research is shown as an example, presenting the most important research results related to the Human Immunodeficiency Virus Type 1 (HIV-1) Vpr protein. Besides, the potential role of fission yeasts in the study of prion biology is also discussed. Furthermore, we are keen to promote the uprising model yeast
, which is a dimorphic species in the fission yeast genus. We propose the hyphal growth of
as an unusual opportunity as a model to study the invadopodia of human cancer cells since the two seemingly different cell types can be compared along fundamental features. Here we also collect the latest laboratory protocols and bioinformatics tools for the fission yeasts to highlight the many possibilities available to the research community. In addition, we present several limiting factors that everyone should be aware of when working with yeast models. |
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ISSN: | 2311-2638 2311-2638 |
DOI: | 10.15698/mic2024.08.833 |