A protein interaction map for cell polarity development

Author:

Drees Becky L.1,Sundin Bryan2,Brazeau Elizabeth1,Caviston Juliane P.3,Chen Guang-Chao4,Guo Wei5,Kozminski Keith G.6,Lau Michelle W.6,Moskow John J.7,Tong Amy8,Schenkman Laura R.9,McKenzie Amos9,Brennwald Patrick10,Longtine Mark11,Bi Erfei3,Chan Clarence4,Novick Peter12,Boone Charles8,Pringle John R.9,Davis Trisha N.2,Fields Stanley13,Drubin David G.6

Affiliation:

1. Departments of Genetics and Medicine, University of Washington, Seattle, WA 98195

2. Department of Biochemistry, University of Washington, Seattle, WA 98195

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

4. Section of Molecular Genetics and Microbiology, Institute for Cellular and Molecular Biology, University of Texas, Austin, TX 78712

5. Biology Department, University of Pennsylvania, Philadelphia, PA 19104

6. Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720

7. Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710

8. Banting and Best Department of Medical Research, University of Toronto, Toronto, Ontario M5G 1L6, Canada

9. Department of Biology, University of North Carolina, Chapel Hill, NC 27599

10. Department of Cell Biology and Genetics, Cornell University, New York, NY 10021

11. Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, OK 74078

12. Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06520

13. Howard Hughes Medical Institute and Departments of Genetics and Medicine, University of Washington, Seattle, WA 98195

Abstract

Many genes required for cell polarity development in budding yeast have been identified and arranged into a functional hierarchy. Core elements of the hierarchy are widely conserved, underlying cell polarity development in diverse eukaryotes. To enumerate more fully the protein–protein interactions that mediate cell polarity development, and to uncover novel mechanisms that coordinate the numerous events involved, we carried out a large-scale two-hybrid experiment. 68 Gal4 DNA binding domain fusions of yeast proteins associated with the actin cytoskeleton, septins, the secretory apparatus, and Rho-type GTPases were used to screen an array of yeast transformants that express ∼90% of the predicted Saccharomyces cerevisiae open reading frames as Gal4 activation domain fusions. 191 protein–protein interactions were detected, of which 128 had not been described previously. 44 interactions implicated 20 previously uncharacterized proteins in cell polarity development. Further insights into possible roles of 13 of these proteins were revealed by their multiple two-hybrid interactions and by subcellular localization. Included in the interaction network were associations of Cdc42 and Rho1 pathways with proteins involved in exocytosis, septin organization, actin assembly, microtubule organization, autophagy, cytokinesis, and cell wall synthesis. Other interactions suggested direct connections between Rho1- and Cdc42-regulated pathways; the secretory apparatus and regulators of polarity establishment; actin assembly and the morphogenesis checkpoint; and the exocytic and endocytic machinery. In total, a network of interactions that provide an integrated response of signaling proteins, the cytoskeleton, and organelles to the spatial cues that direct polarity development was revealed.

Publisher

Rockefeller University Press

Subject

Cell Biology

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