Abstract
Rtg1p is a basic helix-loop-helix transcription factor in the yeast Saccharomyces cerevisiae that is required for basal and regulated expression of CIT2, the gene encoding a peroxisomal isoform of citrate synthase. In respiratory incompetent ρ° petite cells, CIT2 transcription is elevated as much as 30-fold compared with respiratory competent ρ+ cells. Here we provide evidence that Rtg1p interacts directly with a CIT2 upstream activation site (UAS(r)) and that the ρ°/ρ+ regulation is not due to a change in the levels of Rtg1p. A fusion protein consisting of the DNA binding domain of Gal4p fused to the NH2 terminus of the full-length wild-type Rtg1p was able to transactivate an integrated Latz reporter under control of the Gal4p-responsive GAL1 UAS(G) in a ρ°/ρ+dependent manner. Other Gal4p fusions to deletions or mutations of Rtg1p indicate that the helix-loop- helix domain is essential for transactivation. Regulated expression of CIT2 also requires the RTG2 gene product. The Gal4-Rtg1p fusion was unable to transactivate the Latz reporter gene in a strain deleted for RTG2, suggesting that the RTG2 product does not act independently of Rtg1p in the ρ°/ρ+ transcriptional response.
Original language | English (US) |
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Pages (from-to) | 29476-29482 |
Number of pages | 7 |
Journal | Journal of Biological Chemistry |
Volume | 270 |
Issue number | 49 |
DOIs | |
State | Published - 1995 |
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Cell Biology