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Chapter 10: Yeast Two-Hybrid System for Studying Protein–Protein Interactions—References

Brent R. and Ptashne M. 1984. A bacterial repressor protein or a yeast transcriptional terminator can block upstream activation of a yeast gene. Nature 312: 612–615.

Brent R. and Ptashne M. 1985. A eukaryotic transcriptional activator bearing the DNA specificity of a prokaryotic repressor. Cell 43: 729–736.

Chien C.T., Bartel P.L., Sternglanz R., and Fields S. 1991. The two-hybrid system: A method to identify and clone genes for proteins that interact with a protein of interest. Proc. Natl. Acad. Sci. 88: 9578–9582.

Durfee T., Becherer K., Chen P.L., Yeh S.H., Yang Y., Kilburn A.E., Lee W.H., and Elledge S.J. 1993. The retinoblastoma protein associates with the protein phosphatase type 1 catalytic subunit. Genes Dev. 7: 555–569.

Duttweiler H.M. 1996. A highly sensitive and non-lethal beta-galactosidase plate assay for yeast. Trends Genet. 12: 340–341.

Estojak J., Brent R., and Golemis E.A. 1995. Correlation of two-hybrid affinity data with in vitro measurements. Mol. Cell. Biol. 15: 5820–5829.

Fashena S.J., Serebriiskii I.G., and Golemis E.A. 2000. The continued evolution of hybrid screening approaches in yeast: How to outwit different baits with different preys. Gene 250: 1–14.

Fields S. and Song O. 1989. A novel genetic system to detect protein-protein interaction. Nature 340: 245–246.

Finley R. and Brent R. 1994. Interaction mating reveals binary and ternary connections between Drosophila cell cycle regulators. Proc. Natl. Acad. Sci. 91: 12980–12984.

Golemis E.A. and Brent R. 1992. Fused protein domains inhibit DNA binding by LexA. Mol. Cell. Biol. 12: 3006–3014.

Golemis E.A. and Serebriiskii I. 1998. Two-hybrid systems/interaction trap. In Cells: A laboratory manual (ed. D.L. Spector et al.), pp. 69.1–69.40. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.

Golemis E.A., Serebriiskii I., Gyuris J., and Brent R. 1997. Interaction trap/two-hybrid system to identify interacting proteins. In Current protocols in molecular biology (ed. F.M. Ausubel et al.), pp. 20.21.21–20.21.35. Wiley, New York.

Gyuris J., Golemis E.A., Chertkov H., and Brent R. 1993. Cdi1, a human G1 and S phase protein phosphatase that associates with Cdk2. Cell 75: 791–803.

Harlow E. and Lane D. 1988. Antibodies: A laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.

Ma J. and Ptashne M. 1988. Converting a eukaryotic transcriptional inhibitor into an activator. Cell 55: 443–446.

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Sambrook J., Fritsch E.F., and Maniatis T. 1989. Molecular cloning: A laboratory manual, 2nd edition. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.

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Serebriiskii I.G. and Golemis E.A. 2000. Uses of lacZ to study gene function: Evaluation of β-galactosidase assays employed in the yeast two-hybrid system. Anal. Biochem. 285: 1–15.

Serebriiskii I., Khazak V., and Golemis E.A. 1999. A two-hybrid dual bait system to discriminate specificity of protein interactions. J. Biol. Chem. 274: 17080–17087.

Serebriiskii I.G., Toby G.G., and Golemis E.A. 2000a. Streamlined yeast colorimetric reporter assays, using scanners and plate readers. Biotechniques 29: 278–279, 282–274, 286–278.

Serebriiskii I., Estojak J., Berman M., and Golemis E.A. 2000b. Approaches to detecting two-hybrid false positives. Biotechniques 28: 328–336.

Shaywitz D.A., Espenshade P.J., Gimeno R.E., and Kaiser C.A. 1997. COPII subunit interactions in the assembly of the vesicle coat. J. Biol. Chem. 272: 25413–25416.

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West R.W.J., R.R. Yocum, and M. Ptashne. 1984. Saccharomyces cerevisiae GAL1-GAL10 divergent promoter region: Location and function of the upstream activator sequence UAS_G. Mol. Cell. Biol. 4: 2467–2478.

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