Constitutive and inducible Saccharomyces cerevisiae promoters: evidence for two distinct molecular mechanisms
- PMID: 3540601
- PMCID: PMC367147
- DOI: 10.1128/mcb.6.11.3847-3853.1986
Constitutive and inducible Saccharomyces cerevisiae promoters: evidence for two distinct molecular mechanisms
Abstract
his3 and pet56 are adjacent Saccharomyces cerevisiae genes that are transcribed in opposite directions from initiation sites that are separated by 200 base pairs. Under normal growth conditions, in which his3 and pet56 are transcribed at similar basal levels, a poly(dA-dT) sequence located between the genes serves as the upstream promoter element for both. In contrast, his3 but not pet56 transcription is induced during conditions of amino acid starvation, even though the critical regulatory site is located upstream of both respective TATA regions. Moreover, only one of the two normal his3 initiation sites is subject to induction. From genetic and biochemical evidence, I suggest that the his3-pet56 intergenic region contains constitutive and inducible promoters with different properties. In particular, two classes of TATA elements, constitutive (Tc) and regulatory (Tr), can be distinguished by their ability to respond to upstream regulatory elements, by their effects on the selection of initiation sites, and by their physical structure in nuclear chromatin. Constitutive and inducible his3 transcription is mediated by distinct promoters representing each class, whereas pet56 transcription is mediated by a constitutive promoter. Molecular mechanisms for these different kinds of S. cerevisiae promoters are proposed.
Similar articles
-
Naturally occurring poly(dA-dT) sequences are upstream promoter elements for constitutive transcription in yeast.Proc Natl Acad Sci U S A. 1985 Dec;82(24):8419-23. doi: 10.1073/pnas.82.24.8419. Proc Natl Acad Sci U S A. 1985. PMID: 3909145 Free PMC article.
-
Genetic properties and chromatin structure of the yeast gal regulatory element: an enhancer-like sequence.Proc Natl Acad Sci U S A. 1984 Dec;81(24):7865-9. doi: 10.1073/pnas.81.24.7865. Proc Natl Acad Sci U S A. 1984. PMID: 6096864 Free PMC article.
-
Poly(dA).poly(dT) rich sequences are not sufficient to exclude nucleosome formation in a constitutive yeast promoter.Nucleic Acids Res. 1990 Jun 25;18(12):3495-502. doi: 10.1093/nar/18.12.3495. Nucleic Acids Res. 1990. PMID: 2194162 Free PMC article.
-
Mechanism of differential utilization of the his3 TR and TC TATA elements.Mol Cell Biol. 1995 Dec;15(12):7059-66. doi: 10.1128/MCB.15.12.7059. Mol Cell Biol. 1995. PMID: 8524273 Free PMC article.
-
Analysis of Saccharomyces cerevisiae his3 transcription in vitro: biochemical support for multiple mechanisms of transcription.Mol Cell Biol. 1990 Jun;10(6):2832-9. doi: 10.1128/mcb.10.6.2832-2839.1990. Mol Cell Biol. 1990. PMID: 2188101 Free PMC article.
Cited by
-
Yeast and human TATA-binding proteins have nearly identical DNA sequence requirements for transcription in vitro.Mol Cell Biol. 1990 Aug;10(8):3859-67. doi: 10.1128/mcb.10.8.3859-3867.1990. Mol Cell Biol. 1990. PMID: 2196437 Free PMC article.
-
cis- and trans-acting regulatory elements of the yeast URA3 promoter.Mol Cell Biol. 1990 Oct;10(10):5257-70. doi: 10.1128/mcb.10.10.5257-5270.1990. Mol Cell Biol. 1990. PMID: 2204810 Free PMC article.
-
Saturation mutagenesis of a yeast his3 "TATA element": genetic evidence for a specific TATA-binding protein.Proc Natl Acad Sci U S A. 1988 Apr;85(8):2691-5. doi: 10.1073/pnas.85.8.2691. Proc Natl Acad Sci U S A. 1988. PMID: 3282236 Free PMC article.
-
Demonstration of a divergent transcript from the bidirectional heavy chain immunoglobulin promoter VH441 in B-cells.Nucleic Acids Res. 1991 Oct 11;19(19):5339-44. doi: 10.1093/nar/19.19.5339. Nucleic Acids Res. 1991. PMID: 1923817 Free PMC article.
-
Yeast coactivator MBF1 mediates GCN4-dependent transcriptional activation.Mol Cell Biol. 1998 Sep;18(9):4971-6. doi: 10.1128/MCB.18.9.4971. Mol Cell Biol. 1998. PMID: 9710580 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases