Nucleotide Sequence of the 5' Flanking Region Responsible for the Enhancement of the Expression of Yeast Enolase 1 Gene1
- 1 September 1985
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Biochemistry
- Vol. 98 (3) , 859-862
- https://doi.org/10.1093/oxfordjournals.jbchem.a135345
Abstract
Several plasmids carrying different length of the 5' flanking region of yeast (Saccharomyces cerevisiae) enolase 1 gene (ENO1) which is fused in frame to the Escherichia coli lacZ gene were constructed by recombination in vitro. Promoter activity of ENO1 was assayed by measuring β-galactosidase activity of the fused gene product. Comparison of the promoter activity of these plasmids suggests that the sequences required for a strong promoter activity lie within the DNA segment −724 to −353 base pairs (bp) upstream from the start of ENO1 coding sequence. The nucleotide sequence of this region was determined.This publication has 3 references indexed in Scilit:
- A GAL10-CYC1 hybrid yeast promoter identifies the GAL4 regulatory region as an upstream site.Proceedings of the National Academy of Sciences, 1982
- Isolation of yeast histone genes H2A and H2BCell, 1979
- Isolation and identification of yeast messenger ribonucleic acids coding for enolase, glyceraldehyde-3-phosphate dehydrogenase, and phosphoglycerate kinaseBiochemistry, 1978