Skip to main content
Log in

Transformation and recombination in rad mutants of Saccharomyces cerevisiae

  • Published:
Molecular and General Genetics MGG Aims and scope Submit manuscript

Summary

Disruption/deletion mutations in genes of the RAD52 epistasis group of Saccharomyces cerevisiae were examined for their effects on recombination between single-and double-stranded circular DNA substrates and chromosomal genes in a transformation assay. In rad50 mutants there was a small reduction in recombination with single-stranded DNA at the leu2-3, 112 allele; in addition there was an almost complete elimination of recombination at trpl-1 for both single- and double-stranded DNA. Reintroduction of a wild-type RAD50 gene on a replicating plasmid carrying CEN4 restored recombinational competence at trpl-1, indicating that rad50 is defective in gene replacement of this allele. In rad52 mutants a reduction of 30%-50% in recombination involving either single- or double-stranded circular DNA was observed in each experiment when compared to the wild type. This reduction of recombination in rad52 mutants was similar for recombination at the ura352 mutant locus where only integration events have been observed, and at the trpl-1 mutant locus, where recombination occurs predominantly by gene replacement. Neither the rad54 nor the rad57 mutations had a significant effect on recombination with single- or double-stranded DNA substrates.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Adzuma K, Ogawa T, Ogawa H (1984) Primary structure of the RAD52 gene in Saccharomyces cerevisiae. Mol Cell Biol 4:2735–2744

    Google Scholar 

  • Alani E, Subbiah S, Kleckner N (1989) The yeast RAD50 gene encodes a predicted 153 kD protein containing a purine nucleotide-binding domain and two large heptad-repeat regions. Genetics 122:47–57

    Google Scholar 

  • Andreadis A, Hsu Y-P, Kohlhaw GB, Schimmel P (1982) Nucleotide sequences of yeast LEU2 gene shows 5′-noncoding region has sequences cognate to leucine. Cell 31:319–325

    Google Scholar 

  • Boeke JD, Lacroute F, Fink GR (1984) A positive selection for mutants lacking orotidine-5′-phosphate decarboxylase activity in yeast: 5-fluoro-orotic acid resistance. Mol Gen Genet 197:345–346

    CAS  PubMed  Google Scholar 

  • Botstein D, Falco SC, Stewart S, Brennan M, Scherer S, Stinchomb DT, Struhl K (1979) Sterile host yeasts (SHY): a eukaryotic system of biological containment for recombinant DNA experiments. Gene 8:17–24

    Article  CAS  PubMed  Google Scholar 

  • Broach JR, Strathern JA, Hicks JB (1979) Transformation in yeast: development of a hybrid cloning vector and isolation of the CAN1 gene. Gene 8:121–133

    Google Scholar 

  • Calderon IL, Coutopoulou CR, Mortimer RK (1983) Isolation and characterization of yeast DNA repair genes. II. Isolation of plasmids that complement the mutations rad50-1, rad51-1, rad54-3, and rad55-3. Curr Genet 7:93–100

    Google Scholar 

  • Embretson JE, Livingston DM (1984) A plasmid model to study genetic recombination in yeast. Gene 29:293–302

    Google Scholar 

  • Game JC (1983) Radiation-sensitive mutants and DNA repair in yeast. In: Spencer JET, Spencer DM, Smith ARW (eds) Yeast genetics, fundamental and applied aspects. Springer-Verlag, New York, p 109–137

    Google Scholar 

  • Game JC, Mortimer RK (1974) A genetic study of X-ray sensitive mutants in yeast. Mutat Res 24:281–292

    Google Scholar 

  • Game JC, Zamb TS, Braun R, Resnick M, Roth R (1980) The role of radiation (rad) genes in meiotic recombination in yeast. Genetics 94:51–68

    Google Scholar 

  • Hawthorne DC, Leupold U (1974) Suppressors in yeast. Curr Topics Microbiol Immunol 64:1–47

    Google Scholar 

  • Hinnen A, Hicks JB, Fink GR (1978) Transformation of yeast. Proc Natl Acad Sci USA 74:1929–1933

    Google Scholar 

  • Holliday R, Halliwell RE, Evans MW, Rowell V (1976) Genetic characterization of rec-1, a mutant of Ustilago maydis defective in repair and recombination. Genet Res 27:413–453

    Google Scholar 

  • Jackson JA, Fink GR (1981) Gene conversion between duplicated genetic elements in yeast. Nature 292:306–311

    Google Scholar 

  • Kmiec E, Holloman W (1982) Homologous pairing of DNA molecules promoted by a protein from Ustilago. Cell 29:367–374

    Google Scholar 

  • Kunz B, Haynes R (1981) Phenomenology and genetic control of mitotic recombination in yeast. Annual Rev Genet 15:57–89

    Google Scholar 

  • Malone RE (1983) Multiple mutant analysis of recombination in yeast. Mol Gen Genet 189:405–415

    Google Scholar 

  • Malone R, Esposito RE (1980) The RAD52 gene is required for homothallic interconversion of mating types and spontaneous mitotic recombination in yeast. Proc Natl Acad Sci USA 77:503–507

    Google Scholar 

  • Malone RE, Esposito RE (1981) Recombinationless meiosis in Saccharomyces cerevisiae. Mol Cell Biol 1:891–901

    CAS  PubMed  Google Scholar 

  • Malone R, Jordan K, Wardman W (1985) Extragenic revertants of rad50, a yeast mutation causing defects in recombination and repair. Curr Genet 9:453–461

    Google Scholar 

  • Malone RE, Monteleone BA, Edwards C, Carney K, Hoekstra ME (1988) A reexamination of the role of the RAD52 gene in spontaneous mitotic recombination. Curr Genet 14:211–223

    Google Scholar 

  • Messing J (1983) New M13 vectors for cloning. Methods Enzymol 101:20–79

    Article  CAS  PubMed  Google Scholar 

  • Nitiss JL, (1986) Strand breaks and recombination during meiosis in radiation sensitive strains of Saccharomyces cerevisiae. Ph.D. Thesis, Illinois Institute of Technology, Chicago

    Google Scholar 

  • Orr-Weaver T, Szostak J, Rothstein R (1981) Yeast transformation: a model system for the study of recombination. Proc Natl Acad Sci USA 78:6354–6358

    Google Scholar 

  • Prakash L, Taillon-Miller P (1980) Effects of the rad52 gene on sister chromatid recombination in S. cerevisiae. Curr Genet 3:247–250

    Google Scholar 

  • Prakash S, Prakash L, Burke W, Monteleone BA (1980) Effects of the RAD52 gene on recombination in Saccharomyces cerevisiae. Genetics 94:31–50

    Google Scholar 

  • Resnick MA, Martin P (1976) The repair of double-strand breaks in the nuclear DNA of Saccharomyces cerevisiae and its genetic control. Mol Gen Genet 143:119–129

    Google Scholar 

  • Resnick MA, Nitiss J, Edwards C, Malone RE (1986) Meiosis can induce recombination in rad52 mutants of Saccharomyces cerevisiae. Genetics 113:531–550

    Google Scholar 

  • Rose M, Winston F (1984) Identification of a Ty insertion within the coding sequence of the Saccharomyces cerevisiae URA3 gene. Mol Gen Genet 193:557–560

    Google Scholar 

  • Rose M, Grisafi P, Botstein D (1984) Structure and function of the yeast URA3 gene: expression in Escherichia coli. Gene 29:113–124

    Google Scholar 

  • Rothstein RJ (1983) One-step gene disruption in yeast. Methods Enzymol 101:202–211

    Google Scholar 

  • Saeki T, Machida I, Nakai S (1980) Genetic control of diploid recovery after γ-irradiation in the yeast Saccharomyces cerevisiae. Mutat Res 73:251–265

    Google Scholar 

  • Schild D, Calderon IL, Coutopoulou CR, Mortimer RK (1983) Cloning of yeast recombination repair genes and evidence that several are nonessential genes. In: Friedberg EC, Bridges BA (eds) Cellular responses to DNA damage. Liss, New York, pp 417–427

    Google Scholar 

  • Sherman F, Fink GR, Hicks JB (1986) Methods in yeast genetics. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Simon JR, Moore PD (1987) Homologous recombination between single-stranded DNA and chromosomal genes in Saccharomyces cerevisiae. Mol Cell Biol 7:2329–2334

    CAS  PubMed  Google Scholar 

  • Singh H, Baker JJ, Dumas LB (1982) Genetic transformation of Saccharomyces cerevisiae with single-stranded DNA vectors. Gene 20:441–449

    Google Scholar 

  • Southern EH (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 95:503–517

    Google Scholar 

  • Stinchcomb DT, Struhl K, Davis RW (1976) Isolation and characterization of a yeast chromosomal replicator. Nature 282:1035–1039

    Google Scholar 

  • Stinchcomb DT, Thomas M, Kelly J, Selker E, Davis RW (1980) Eukaryotic DNA segments capable of autonomous replication in yeast. Proc Natl Acad Sci USA 77:4559–4563

    Google Scholar 

  • Strike TL (1978) Characterization of mutants of yeast sensitive to X-rays. PhD Thesis, University of California, Davis

    Google Scholar 

  • Sugino A, Nitiss J, Resnick MA (1988) ATP independent DNA strand transfer catalyzed by protein(s) from meiotic cells of the yeast Saccharomyces cerevisiae. Proc Natl Acad Sci USA 85:3683–3687

    Google Scholar 

  • Tschumper G, Carbon J (1980) Sequence of a yeast DNA fragment containing a chromosomal replicator and the TRP1 gene. Gene 10:157–166

    Google Scholar 

  • Yanisch-Perron C, Vieira J, Messing J (1985) Improved M13 vectors and host strains: nucleotide sequences of the Ml3mp18 and pUC19 vectors. Gene 33:103–119

    Article  CAS  PubMed  Google Scholar 

  • Zamb TJ, Petes TD (1981) Unequal sister-strand recombination with yeast ribosomal DNA does not require the RAD52 gene product. Curr Genet 3:125–132

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by G.R. Smith

Rights and permissions

Reprints and permissions

About this article

Cite this article

Simon, J.R., Moore, P.D. Transformation and recombination in rad mutants of Saccharomyces cerevisiae . Molec. Gen. Genet. 223, 241–248 (1990). https://doi.org/10.1007/BF00265060

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00265060

Key words

Navigation