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PMID: 1985916 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Sequence-specific transcriptional antirepression of the Drosophila Krüppel gene by the GAGA factor.

The Journal of biological chemistry ·Vol. 266 ·No. 1 ·1991-01-05 ·Pages 574-82

Kerrigan LA, Croston GE, Lira LM, Kadonaga JT

Abstract

We have analyzed the proximal promoter of the Drosophila Krüppel (Kr) gene. A 44-base pair fragment containing the RNA start sites contains significant promoter activity, and this minimal promoter is flanked both upstream and downstream by binding sites for the GAGA factor. The GAGA factor is the predominant sequence-specific DNA binding factor that interacts with the Kr promoter region, and the purified protein activates Kr transcription in vitro. However, strong transcriptional activation of Kr as well as of Ultrabithorax, another GAGA factor-responsive gene, requires the presence of a DNA binding transcriptional repressor. The GAGA factor is able to relieve this repression in a binding site-dependent manner, and, thus, these data suggest that the GAGA factor functions as an antirepressor, rather than an activator, of the Kr gene.

Related Genes
Kr
MeSH Terms
Animals Base Sequence Binding Sites DNA/genetics,isolation & purification DNA-Binding Proteins/metabolism Drosophila/genetics Genes Molecular Sequence Data Oligonucleotide Probes Promoter Regions, Genetic Templates, Genetic Transcription, Genetic
Chemicals
DNA-Binding Proteins Oligonucleotide Probes DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kerrigan L A
Department of Biology, University of California at San Diego, La Jolla 92093.
Croston G E
Lira L M
Kadonaga J T
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1991-01-05
Pages
574-82
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM 41249 · United States
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