Abstract

Protein–protein interactions play pivotal roles in various aspects of the structural and functional organization of the cell, and their complete description is indispensable to thorough understanding of the cell. As an approach toward this goal, here we report a comprehensive system to examine two-hybrid interactions in all of the possible combinations between proteins of Saccharomyces cerevisiae . We cloned all of the yeast ORFs individually as a DNA-binding domain fusion (“bait”) in a MAT a strain and as an activation domain fusion (“prey”) in a MAT α strain, and subsequently divided them into pools, each containing 96 clones. These bait and prey clone pools were systematically mated with each other, and the transformants were subjected to strict selection for the activation of three reporter genes followed by sequence tagging. Our initial examination of ≈4 × 10 6 different combinations, constituting ≈10% of the total to be tested, has revealed 183 independent two-hybrid interactions, more than half of which are entirely novel. Notably, the obtained binary data allow us to extract more complex interaction networks, including the one that may explain a currently unsolved mechanism for the connection between distinct steps of vesicular transport. The approach described here thus will provide many leads for integration of various cellular functions and serve as a major driving force in the completion of the protein–protein interaction map.

Keywords

Saccharomyces cerevisiaeBiologyORFSBudding yeastProtein–protein interactionYeastComputational biologyTandem affinity purificationFusion proteinGeneticsProtein domainProtein-fragment complementation assayTwo-hybrid screeningGeneCell biologyPeptide sequenceBiochemistryPhenotypeComplementationOpen reading frameRecombinant DNA

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Publication Info

Year
2000
Type
article
Volume
97
Issue
3
Pages
1143-1147
Citations
807
Access
Closed

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Takashi Ito, Kosuke Tashiro, Shigeru Muta et al. (2000). Toward a protein–protein interaction map of the budding yeast: A comprehensive system to examine two-hybrid interactions in all possible combinations between the yeast proteins. Proceedings of the National Academy of Sciences , 97 (3) , 1143-1147. https://doi.org/10.1073/pnas.97.3.1143

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DOI
10.1073/pnas.97.3.1143