Title | Interchangeable RNA polymerase I and II enhancers. |
Publication Type | Journal Article |
Year of Publication | 1990 |
Authors | Lorch Y, Lue NF, Kornberg RD |
Journal | Proc Natl Acad Sci U S A |
Volume | 87 |
Issue | 21 |
Pagination | 8202-6 |
Date Published | 1990 Nov |
ISSN | 0027-8424 |
Keywords | Base Sequence, Enhancer Elements, Genetic, Escherichia coli, Genetic Vectors, Molecular Sequence Data, Oligonucleotide Probes, Plasmids, Restriction Mapping, RNA Polymerase I, RNA Polymerase II, Saccharomyces cerevisiae |
Abstract | The RNA polymerase I (pol I) enhancer of Saccharomyces cerevisiae contains at least three elements commonly associated with RNA polymerase II (pol II) enhancers, binding sites for the transcriptional activators general regulatory factor 2 and autonomously replicating sequence-binding factor I, and a thymidine-rich element. When the particular form of the thymidine-rich element found in the pol I enhancer was placed in front of a pol II promoter, transcription was stimulated 43-fold, comparable to the effect of a powerful pol II activator such as Gal4. Conversely, when two copies of a thymidine-rich element from a pol II enhancer were placed upstream of a pol I promoter, transcription was stimulated 38-fold. This functional reciprocity of pol I and II enhancers may reflect similarities in the mechanisms of transcriptional activation. The pol I enhancer also contains an element that appears to be pol I-specific and prevent the activation of pol II. |
DOI | 10.1073/pnas.87.21.8202 |
Alternate Journal | Proc Natl Acad Sci U S A |
PubMed ID | 2236033 |
PubMed Central ID | PMC54923 |
Grant List | GM36659 / GM / NIGMS NIH HHS / United States |
Submitted by jom4013 on December 3, 2020 - 4:18pm