Systematic analysis of Ca2+homeostasis inSaccharomyces cerevisiaebased on chemical-genetic interaction profiles

Author:

Ghanegolmohammadi Farzan1,Yoshida Mitsunori1,Ohnuki Shinsuke1,Sukegawa Yuko12,Okada Hiroki13,Obara Keisuke4,Kihara Akio4,Suzuki Kuninori15,Kojima Tetsuya1,Yachie Nozomu67,Hirata Dai89,Ohya Yoshikazu1

Affiliation:

1. Department of Integrated Biosciences, University of Tokyo, Kashiwa 277-8562, Japan

2. AIST-UTokyo Advanced Operand-Measurement Technology Open Innovation Laboratory, Kashiwa 277-0882, Japan

3. Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104-6058

4. Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan

5. Bioimaging Center, Graduate School of Frontier Sciences, University of Tokyo, Kashiwa 277-8562, Japan

6. Synthetic Biology Division, Research Center for Advanced Science and Technology, University of Tokyo, Tokyo 153-8904, Japan

7. PRESTO, Japan Science and Technology Agency, Tokyo 102-0076, Japan

8. Research and Development Department, Asahi Sake Brewing Co., Nagaoka 949-5494, Japan

9. Department of Molecular Biotechnology, Graduate School of Advanced Sciences of Matter, Hiroshima University, Higashi-Hiroshima 739-8530, Japan

Abstract

We investigated the global landscape of Ca2+homeostasis in budding yeast based on high-dimensional chemical-genetic interaction profiles. The morphological responses of 62 Ca2+-sensitive (cls) mutants were quantitatively analyzed with the image processing program CalMorph after exposure to a high concentration of Ca2+. After a generalized linear model was applied, an analysis of covariance model was used to detect significant Ca2+–cls interactions. We found that high-dimensional, morphological Ca2+–cls interactions were mixed with positive (86%) and negative (14%) chemical-genetic interactions, whereas one-dimensional fitness Ca2+–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 Ca2+–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 Ca2+-sensitive phenotypes triggered by inactivation of calcineurin, a Ca2+-dependent phosphatase. Finally, similarity of the interaction profiles was used to reveal a connected network among the Ca2+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 Ca2+homeostasis.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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