Abstract
The yeasts S. cerevisiae and Schizosaccharomyces pombe are non-pathogenic, prevalently haploid unicellular fungi that grow and form colonies on defined media. Both organisms have been for decades favoured objects of investigation, first by classical genetics and more recently by molecular techniques. Knowledge accumulated, specially over the last few years, has revealed that both yeasts, not only clarify mechanisms of genetic transmission (gene expression, mitosis and meiosis) and signal transduction common to higher eukaryotes but, unexpectedly, also illuminate many processes crucial to the development of multicellular organisms such as cell differentiation and cell-cell interactions. Many elements (proteins, cis acting elements) of the control circuits of the cell are conserved from yeast to mammals; remarkably, in many cases, yeast control elements can be replaced with elements of heterologous control circuits. It is thus possible to isolate genes from higher eukaryotes by complementation and to scrutinize their function by the powerful genetics now available in both yeasts.
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References
Arndt K and Fink G (1986) GCN4 protein, a positive transcription factor in yeast, binds general control promoters at all 5’ TGACTC 3’ sequences. Proc. Natl. Acad. Sci. USA 83: 8516–8520.
Becker DM, Fikes JD and Guarente L (1991) A cDNA encoding a human CAAT-binding protein cloned by functional complementation in yeast. Proc. Natl. Acad. Sci. USA 88: 1968.
Broek D, Toda T, Michaeli T, Levin L, Birchmeier C, Zoller M, Powers S and Wigler M (1987) The S. cerevisiae CDC25 gene product regulates the RAS/adenylate cyclase pathway. Cell 48: 789–799.
Buratowski S, Hahn S, Sharp PA and Guarente L (1988) Function of a yeast TATA element-binding protein in a mammalian transcription system. Nature 334: 37–42.
Chen W and Struhl K (1985) Yeast mRNA initiation sites are determined primarily by specific sequences, not by the distance from the TATA element. EMBO J. 4: 3273–3280.
Ciaramella M, Sacco M and Pulitzer JF (1988) Foreign transcriptional enhancers in yeast. I. Interactions of papovavirus transcriptional enhancers and a quiescent pseudopromoter on supercoiled plasmids. Nucl. Acids Res. 16: 8847–8868.
DeFeo Jones D, Scolnick EM, Koller R and Dhar R (1983) ras-related gene sequences identified and isolated from Saccharomyces cerevisiae. Nature 306: 707–709.
Dunphy WG and Kumagai A (1991) The cdc25 protein contains an intrinsic phosphatase activity. Cell 67: 189–196.
Geiser JR, van Tuinen D, Brockerhoff SE, Neff MM and Davis TN (1991) Can calmodulin function without binding calcium? Cell 65: 949–959.
Gould KL, Moreno S, Tonks NK and Nurse P (1990) Complementation of the mitotic activator, p80cdc25, by a human protein-tyrosine phosphatase. Science 250: 1573–1576.
Hahn S and Guarente L (1988) Yeast HAP2 and HAP3: transcriptional activators in a heteromeric complex. Science 240: 317–321
Hall A (1990) The cellular functions of small GTP-binding proteins. Science 249: 635–640.
Hope I and Struhl K (1985) GCN4 protein, synthesized in vitro, binds HIS3 regulatory sequences: implications for general control of amino acid biosynthetic genes in yeast. Cell 43: 177–188.
Hughes DA, Fukui Y, Yamamoto M (1990) Homologous activators of ras in fission and budding yeast. Nature 344 6264: 355–357.
Kataoka T, Powers S, Cameron S, Fasano O, Goldfarb M, Broach J and Wigler M (1985) Functional homology of mammalian and yeast RAS genes. Cell 40:19–26.
Lee MG and Nurse P (1988) Complementation used to clone a human homologue of the fission yeast cell cycle control gene cdc2. Nature 327: 31–35.
Leopold P and O’Farrell PH (1991) An evolutionarily conserved cyclin homolog from Drosophila rescues yeast deficient in G1 cyclins. Cell 66: 1207–1216.
Nagawa F and Fink GR (1985) The relationship between the “TATA” sequence and transcription initiation sites at the HIS4 gene of Saccharomyces cerevisiae. Proc. Natl. Acad. Sci. USA, 82: 8557–8561.
Powers S, O’Neill K and Wigler M (1989) Dominant yeast and mammalian RAS mutants that interfere with the CDC25-dependent activation of wild-type RAS in Saccharomyces cerevisiae. Mol. Cell. Biol. 9: 390–395.
Pringle JR and Hartwell LH (1982) The Saccharomyces cerevisiae life cycle. In The Molecular Biology of the Yeast S. Cerevisiae Cold Spring Harbor Lab. (J.N. Strathern et al. Eds) p. 97-142.
Pugh BF and Tjian R (1992) Diverse transcriptional functions of the multisubunit eukaryotic TFIID complex. J. Biol. Chem. 267: 679.
Struhl K (1987a) The DNA-binding domains of the jun oncoprotein and the yeast GCN4 transcriptional activator protein are functionally homologous. Cell 50: 841–846.
Struhl K (1987b) Promoters, activator proteins, and the mechanism of transcriptional initiation in yeast. Cell 49:295–297.
Toda T, Uno I, Ishikawa T, Powers S, Kataoka T, Broek D, Cameron S, Broach J, Matsumoto K and Wigler M (1985) In yeast, RAS proteins are controlling elements of adenylate cyclase. Cell 40: 27–36.
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© 1993 Springer-Verlag Berlin Heidelberg
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Pulitzer, J.F., Pollice, A. (1993). Gene regulatory circuits in Saccharomyces cerevisiae as a tool for the identification of heterologous eukaryotic regulatory elements. In: Maresca, B., Kobayashi, G.S., Yamaguchi, H. (eds) Molecular Biology and its Application to Medical Mycology. NATO ASI Series, vol 69. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-84625-0_10
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DOI: https://doi.org/10.1007/978-3-642-84625-0_10
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