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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Nature
Article . 1994 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
Nature
Article . 1994
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An HMG-like protein that can switch a transcriptional activator to a repressor

Authors: Joshua M. Brickman; Norbert Lehming; Tom Maniatis; Dimitris Thanos; Mark Ptashne; Jun Ma; Jun Ma;

An HMG-like protein that can switch a transcriptional activator to a repressor

Abstract

One protein can activate some genes and repress others in the same cell. The Drosophila protein Dorsal (which, like the human protein NF-kappa B3, is a member of the Rel family of transcriptional activators) activates the twist gene and represses the zen gene in the ventral region of early embryos. Here we describe a Drosophila HMG1 protein, called DSP1 (dorsal switch protein), that converts Dorsal and NF-kappa B from transcriptional activators to repressors. This effect requires a sequence termed a negative regulatory element (NRE), found adjacent to Dorsal-binding sites in the zen promoter and adjacent to the NF-kappa B-binding site in the human interferon-beta (IFN-beta) enhancer. Previous studies have shown that another type of HMG protein, HMG I(Y), can stimulate NF-kappa B activity. Thus, the HMG-like proteins DSP1 and HMG I(Y) can determine whether a specific regulator functions as an activator or a repressor of transcription.

Related Organizations
Keywords

Base Sequence, Molecular Sequence Data, High Mobility Group Proteins, NF-kappa B, Nuclear Proteins, DNA, Interferon-beta, Phosphoproteins, Recombinant Proteins, Repressor Proteins, Enhancer Elements, Genetic, Animals, Drosophila Proteins, Humans, Drosophila, Amino Acid Sequence, HMGA1a Protein, Promoter Regions, Genetic, HeLa Cells, Protein Binding

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Powered by OpenAIRE graph
citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
227
Top 10%
Top 1%
Top 1%