Home LiteratureArticle Details
PMID: 6396505 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Upstream region required for regulated expression of the glucose-repressible SUC2 gene of Saccharomyces cerevisiae.

Molecular and cellular biology ·Vol. 4 ·No. 12 ·1984-12-00 ·Pages 2750-7

Sarokin L, Carlson M

Abstract

The SUC2 gene produces two mRNAs with different 5' ends that encode two forms of invertase. The 1.9-kilobase mRNA encoding secreted invertase is regulated by glucose repression (carbon catabolite repression), and the 1.8-kilobase mRNA encoding intracellular invertase is produced constitutively at low levels. To identify 5' noncoding sequences essential for regulated expression of SUC2, we constructed in vitro a series of deletions and inserted them into the yeast genome at the chromosomal SUC2 locus. Analysis of the effects of each deletion on SUC2 gene expression identified an upstream region required for derepression of secreted invertase synthesis. The 3' boundary of this region is near -418. The 5' boundary does not appear to be sharply defined, but lies ca. 100 base pairs upstream. A deletion extending from -418 to -140 allowed high-level derepression, indicating that no essential sequences lie between the upstream region and the TATA box at -133 and that the upstream region can be moved 279 base pairs closer to the transcriptional start site. Interactions between the deletions and several unlinked mutations affecting the regulation of SUC2 gene expression were examined. Sequences between -1,900 and -86 are dispensable for expression of the 1.8-kilobase mRNA.

MeSH Terms
Base Sequence Chromosome Deletion Gene Expression Regulation/drug effects Glucose/pharmacology Glycoside Hydrolases/metabolism Mutation Nucleic Acid Conformation Plasmids Saccharomyces cerevisiae/genetics beta-Fructofuranosidase
Chemicals
Glycoside Hydrolases beta-Fructofuranosidase Glucose
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sarokin L
Carlson M
References (20)
20 references, click to expand
  1. Determination of enzymatic activity in polyacrylamide gels. I. Enzymes catalyzing the conversion of nonreducing substrates to reducing products.
    Anal Biochem. 1969 Mar;27(3):545-54 PMID: 4304181
  2. Beta-D-fructofuranoside fructohydrolase from yeast.
    Methods Enzymol. 1975;42:504-11 PMID: 237205
  3. Detection of specific sequences among DNA fragments separated by gel electrophoresis.
    J Mol Biol. 1975 Nov 5;98(3):503-17 PMID: 1195397
  4. Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.
    J Mol Biol. 1977 Jun 15;113(1):237-51 PMID: 881736
  5. Transformation of yeast.
    Proc Natl Acad Sci U S A. 1978 Apr;75(4):1929-33 PMID: 347451
  6. Preparative and analytical purification of DNA from agarose.
    Proc Natl Acad Sci U S A. 1979 Feb;76(2):615-9 PMID: 284385
  7. 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
  8. Sterile host yeasts (SHY): a eukaryotic system of biological containment for recombinant DNA experiments.
    Gene. 1979 Dec;8(1):17-24 PMID: 395030
  9. Rapid DNA isolations for enzymatic and hybridization analysis.
    Methods Enzymol. 1980;65(1):404-11 PMID: 6246361
  10. Sequencing end-labeled DNA with base-specific chemical cleavages.
    Methods Enzymol. 1980;65(1):499-560 PMID: 6246368
  11. Presecretory and cytoplasmic invertase polypeptides encoded by distinct mRNAs derived from the same structural gene differ by a signal sequence.
    Proc Natl Acad Sci U S A. 1982 Feb;79(3):781-5 PMID: 7038684
  12. Two differentially regulated mRNAs with different 5' ends encode secreted with intracellular forms of yeast invertase.
    Cell. 1982 Jan;28(1):145-54 PMID: 7039847
  13. Mutants of yeast defective in sucrose utilization.
    Genetics. 1981 May;98(1):25-40 PMID: 7040163
  14. Characterization of a regulatory region upstream of the ADR2 locus of S. cerevisiae.
    Nature. 1982 Dec 23;300(5894):724-8 PMID: 6757760
  15. Nucleotide sequence of the yeast SUC2 gene for invertase.
    Nucleic Acids Res. 1983 Mar 25;11(6):1943-54 PMID: 6300785
  16. The secreted form of invertase in Saccharomyces cerevisiae is synthesized from mRNA encoding a signal sequence.
    Mol Cell Biol. 1983 Mar;3(3):439-47 PMID: 6341817
  17. Eviction and transplacement of mutant genes in yeast.
    Methods Enzymol. 1983;101:211-28 PMID: 6310325
  18. Distinctly regulated tandem upstream activation sites mediate catabolite repression of the CYC1 gene of S. cerevisiae.
    Cell. 1984 Feb;36(2):503-11 PMID: 6319028
  19. Cloning and genetic mapping of SNF1, a gene required for expression of glucose-repressible genes in Saccharomyces cerevisiae.
    Mol Cell Biol. 1984 Jan;4(1):49-53 PMID: 6366512
  20. A suppressor of SNF1 mutations causes constitutive high-level invertase synthesis in yeast.
    Genetics. 1984 May;107(1):19-32 PMID: 6373495
Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1984-12-00
Pages
2750-7
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC369285
Subset
IM
Grants
NIGMS NIH HHS · GM07088 · United States
NIGMS NIH HHS · GM32065 · United States
Databases
GENBANK
K03294
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: [email protected]