Home LiteratureArticle Details
PMID: 3923299 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Expression of the RAD1 and RAD3 genes of Saccharomyces cerevisiae is not affected by DNA damage or during the cell division cycle.

Molecular & general genetics : MGG ·Vol. 199 ·No. 1 ·1985-00-00 ·Pages 59-63

Nagpal ML, Higgins DR, Prakash S

Abstract

The RAD1 and RAD3 genes of Saccharomyces cerevisiae are required for excision repair of UV damaged DNA. In addition, the RAD3 gene is essential since rad3 deletions are recessive lethals. We have examined the induction of the RAD1 and RAD3 genes by DNA damage and during the cell division cycle. We have made fusions of the RAD1 and RAD3 genes with the Escherichia coli lacZ gene encoding beta-galactosidase. Beta-galactosidase activity was measured in a Rad+ yeast strain containing the RAD1-lacZ or the RAD3-lacZ fusion, either in a multicopy replicating plasmid or as a single copy integrant resulting from transformation with an integrating plasmid which transforms yeast by homologous recombination in the yeast genome. No induction of beta-galactosidase activity occurred after ultraviolet light (UV) or 4-nitroquinoline-1-oxide (NQO) treatment. Haploid cells of mating type a were synchronized by treatment with alpha factor and beta-galactosidase activity was determined during different cell cycle stages. No change in beta-galactosidase activity was observed in the strain containing the RAD1-lacZ or the RAD3-lacZ fusion integrated in the yeast genome.

MeSH Terms
4-Nitroquinoline-1-oxide/toxicity Cell Cycle DNA Repair DNA, Fungal/genetics,radiation effects DNA, Recombinant Gene Expression Regulation Genes, Fungal Genes, Mating Type, Fungal Saccharomyces cerevisiae/genetics Ultraviolet Rays beta-Galactosidase/genetics
Chemicals
DNA, Fungal DNA, Recombinant 4-Nitroquinoline-1-oxide beta-Galactosidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nagpal M L
Higgins D R
Prakash S
References (24)
24 references, click to expand
  1. Replacement of chromosome segments with altered DNA sequences constructed in vitro.
    Proc Natl Acad Sci U S A. 1979 Oct;76(10):4951-5 PMID: 388424
  2. Expression of the E. coli uvrA gene is inducible.
    Nature. 1981 Feb 26;289(5800):808-10 PMID: 6780917
  3. Repair of interstrand cross-links in DNA of Saccharomyces cerevisiae requires two systems for DNA repair: the RAD3 system and the RAD51 system.
    Mol Gen Genet. 1981;182(2):196-205 PMID: 7026973
  4. Transcription of the uvrD gene of Escherichia coli is controlled by the lexA repressor and by attenuation.
    Nucleic Acids Res. 1983 Dec 20;11(24):8625-40 PMID: 6324092
  5. A DNA repair gene required for the incision of damaged DNA is essential for viability in Saccharomyces cerevisiae.
    Proc Natl Acad Sci U S A. 1983 Aug;80(15):4818-21 PMID: 6308653
  6. In vivo regulation of the uvrA gene: role of the "-10" and "-35" promoter regions.
    Nucleic Acids Res. 1983 Sep 10;11(17):5795-810 PMID: 6310514
  7. Construction and use of gene fusions to lacZ (beta-galactosidase) that are expressed in yeast.
    Methods Enzymol. 1983;101:167-80 PMID: 6310320
  8. Isolation and characterization of the RAD3 gene of Saccharomyces cerevisiae and inviability of rad3 deletion mutants.
    Proc Natl Acad Sci U S A. 1983 Sep;80(18):5680-4 PMID: 16593371
  9. Molecular cloning and characterization of the RAD1 gene of Saccharomyces cerevisiae.
    Gene. 1983 Dec;26(2-3):119-26 PMID: 6368317
  10. Specific Saccharomyces cerevisiae genes are expressed in response to DNA-damaging agents.
    Mol Cell Biol. 1985 Jan;5(1):75-84 PMID: 3920512
  11. The fate of 8-methoxypsoralen photoinduced crosslinks in nuclear and mitochondrial yeast DNA: comparison of wild-type and repair-deficient strains.
    Proc Natl Acad Sci U S A. 1982 Mar;79(6):1722-6 PMID: 6281782
  12. Replication of the nuclear genome in yeast does not require concomitant protein synthesis.
    Biochem Biophys Res Commun. 1973 Jun 8;52(3):731-40 PMID: 4575782
  13. Regulation of CDC9, the Saccharomyces cerevisiae gene that encodes DNA ligase.
    Mol Cell Biol. 1985 Jan;5(1):226-35 PMID: 3885010
  14. Incision and postincision steps of pyrimidine dimer removal in excision-defective mutants of Saccharomyces cerevisiae.
    J Bacteriol. 1981 Nov;148(2):618-23 PMID: 7028721
  15. The Escherichia coli uvrD gene is inducible by DNA damage.
    Mol Gen Genet. 1983;191(3):397-400 PMID: 6355763
  16. The uvrB gene of Escherichia coli has both lexA-repressed and lexA-independent promoters.
    Cell. 1982 Mar;28(3):523-30 PMID: 6280873
  17. Regulation of the Escherichia coli K-12 uvrB operon.
    J Bacteriol. 1982 May;150(2):676-85 PMID: 6802798
  18. In vitro gene fusions that join an enzymatically active beta-galactosidase segment to amino-terminal fragments of exogenous proteins: Escherichia coli plasmid vectors for the detection and cloning of translational initiation signals.
    J Bacteriol. 1980 Aug;143(2):971-80 PMID: 6162838
  19. recA+ gene-dependent regulation of a uvrD::lacZ fusion in Escherichia coli K12.
    Mol Gen Genet. 1983;192(3):391-4 PMID: 6361489
  20. Genetic control of excision of Saccharomyces cerevisiae interstrand DNA cross-links induced by psoralen plus near-UV light.
    Mol Cell Biol. 1982 Aug;2(8):939-48 PMID: 6752694
  21. Specific transcripts are elevated in Saccharomyces cerevisiae in response to DNA damage.
    Mol Cell Biol. 1984 Nov;4(11):2356-63 PMID: 6440006
  22. Molecular mechanisms of pyrimidine dimer excision in Saccharomyces cerevisiae: incision of ultraviolet-irradiated deoxyribonucleic acid in vivo.
    J Bacteriol. 1981 May;146(2):692-704 PMID: 7012136
  23. Yeast promoters and lacZ fusions designed to study expression of cloned genes in yeast.
    Methods Enzymol. 1983;101:181-91 PMID: 6310321
  24. Sterile host yeasts (SHY): a eukaryotic system of biological containment for recombinant DNA experiments.
    Gene. 1979 Dec;8(1):17-24 PMID: 395030
Article Info
Journal
Molecular & general genetics : MGG
Abbr.
Mol Gen Genet
ISSN
0026-8925
Published
1985-00-00
Pages
59-63
Language
English
Region
Germany
NLM ID
0125036
Subset
IM
Grants
NCI NIH HHS · CA 35035 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com