Yeast-based assays for the functional characterization of cancer-associated variants of human DNA repair genes

Microb Cell. 2020 May 18;7(7):162-174. doi: 10.15698/mic2020.07.721.

Abstract

Technological advances are continuously revealing new genetic variants that are often difficult to interpret. As one of the most genetically tractable model organisms, yeast can have a central role in determining the consequences of human genetic variation. DNA repair gene mutations are associated with many types of cancers, therefore the evaluation of the functional impact of these mutations is crucial for risk assessment and for determining therapeutic strategies. Owing to the evolutionary conservation of DNA repair pathways between human cells and the yeast Saccharomyces cerevisiae, several functional assays have been developed. Here, we describe assays for variants of human genes belonging to the major DNA repair pathways divided in functional assays for human genes with yeast orthologues and human genes lacking a yeast orthologue. Human genes with orthologues can be studied by introducing the correspondent human mutations directly in the yeast gene or expressing the human gene carrying the mutations; while the only possible approach for human genes without a yeast orthologue is the heterologous expression. The common principle of these approaches is that the mutated gene determines a phenotypic alteration that can vary according to the gene studied and the domain of the protein. Here, we show how the versatility of yeast can help in classifying cancer-associated variants.

Keywords: Saccharomyces cerevisiae; cancer-associated variants; functional assays; human DNA repair genes; humanized yeast strains.

Publication types

  • Review

Grants and funding

The authors wish to thank all the members of the laboratory for suggestions and comments. Special thanks to Marcella Simili and Michael Minks for critical reading and language editing. The work in the lab is supported by the grant 127/16 funded by the “Fondazione Pisa” assigned to AG.