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Systematic analysis of Ca(2+) homeostasis in Saccharomyces cerevisiae based on chemical-genetic interaction profiles
We investigated the global landscape of Ca(2+) homeostasis in budding yeast based on high-dimensional chemical-genetic interaction profiles. The morphological responses of 62 Ca(2+)-sensitive (cls) mutants were quantitatively analyzed with the image processing program CalMorph after exposure to a hi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687040/ https://www.ncbi.nlm.nih.gov/pubmed/28566553 http://dx.doi.org/10.1091/mbc.E17-04-0216 |
Sumario: | We investigated the global landscape of Ca(2+) homeostasis in budding yeast based on high-dimensional chemical-genetic interaction profiles. The morphological responses of 62 Ca(2+)-sensitive (cls) mutants were quantitatively analyzed with the image processing program CalMorph after exposure to a high concentration of Ca(2+). After a generalized linear model was applied, an analysis of covariance model was used to detect significant Ca(2+)–cls interactions. We found that high-dimensional, morphological Ca(2+)–cls interactions were mixed with positive (86%) and negative (14%) chemical-genetic interactions, whereas one-dimensional fitness Ca(2+)–cls interactions were all negative in principle. Clustering analysis with the interaction profiles revealed nine distinct gene groups, six of which were functionally associated. In addition, characterization of Ca(2+)–cls interactions revealed that morphology-based negative interactions are unique signatures of sensitized cellular processes and pathways. Principal component analysis was used to discriminate between suppression and enhancement of the Ca(2+)-sensitive phenotypes triggered by inactivation of calcineurin, a Ca(2+)-dependent phosphatase. Finally, similarity of the interaction profiles was used to reveal a connected network among the Ca(2+) homeostasis units acting in different cellular compartments. Our analyses of high-dimensional chemical-genetic interaction profiles provide novel insights into the intracellular network of yeast Ca(2+) homeostasis. |
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