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Journal ArticleDOI

The COUP transcription factor binds to an upstream promoter element of the rat insulin II gene.

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TLDR
Band-shifting and DNase I-footprinting assays have been used to study the trans-acting factor(s) binding to an important promoter element of the rat insulin II gene, and the binding sequences of the COUP transcription factor in the ovalbumin and the insulin promoters have only limited similarities.
Abstract
Band-shifting and DNase I-footprinting assays have been used to study the trans-acting factor(s) binding to an important promoter element (-53 to -46 relative to the transcription start) of the rat insulin II gene. A binding activity which footprints a region between -60 and -40 was found in both HIT, a hamster insulinoma cell line, and HeLa cells. A mutation within this region which drastically decreases promoter activity in vivo also greatly reduces binding activity in vitro. This binding activity was purified from HeLa cells and identified by competition and renaturation analyses as being the same as the COUP (chicken ovalbumin upstream promoter) transcription factor, a DNA-binding protein required for efficient transcription of the ovalbumin gene in vitro. Interestingly, the binding sequences of the COUP transcription factor in the ovalbumin and the insulin promoters have only limited similarities.

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Citations
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Orphan nuclear receptors: from gene to function.

TL;DR: I. Nuclear Receptors: General Concepts and Orphans in Search of a Home.
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Tissue-specific regulation of the insulin gene by a novel basic helix-loop-helix transcription factor.

TL;DR: A modified yeast two-hybrid system was utilized to clone a novel bHLH factor, BETA2 (beta-cell E-box trans-activator 2), from a hamster insulin tumor (HIT) cell cDNA library, and northern analysis demonstrates that high-level expression of the BETA 2 gene is restricted to pancreatic alpha- and beta-cell lines.
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Identification of the DNA binding site for NGFI-B by genetic selection in yeast.

TL;DR: An in vivo selection system for isolating targets of DNA binding proteins in yeast was developed and used to identify the DNA binding site for the NGFI-B protein, a member of the steroid-thyroid hormone receptor superfamily.
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The steroid receptor superfamily: more excitement predicted for the future.

TL;DR: This superfamily of regulatory molecules was shown to include also the receptors for thyroid hormone (T3) vitamin D3 and retinoic acid and perhaps more surprising was the inclusion of oncogenes such as v-erb A in this family.
Journal ArticleDOI

COUP transcription factor is a member of the steroid receptor superfamily.

TL;DR: It is concluded that this superfamily of gene regulators contains proteins which bind and activate distal promoter elements of eukaryotic genes, and COUP-TF is the first member of this family that has been shown to function in a cell–free transcription system.
References
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Journal ArticleDOI

Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells.

TL;DR: A series of recombinant genomes which directed expression of the enzyme chloramphenicol acetyltransferase (CAT) in mammalian cells provided a uniquely convenient system for monitoring the expression of foreign DNAs in tissue culture cells.
Journal ArticleDOI

Genetic regulatory mechanisms in the synthesis of proteins.

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Multiple nuclear factors interact with the immunoglobulin enhancer sequences.

TL;DR: In this paper, an electrophoretic mobility shift assay with end-labeled DNA fragments was used to characterize proteins that bind to the immunoglobulin (Ig) heavy chain and the kappa light chain enhancers.
Journal ArticleDOI

Regulation of inducible and tissue-specific gene expression

TL;DR: A number of cases of inducible and tissue-specific gene expression involve the activation of preexisting transcription factors, rather than the synthesis of new proteins, which may involve covalent modification of the protein or an allosteric change in its structure.
Journal ArticleDOI

Heritable formation of pancreatic β -cell tumours in transgenic mice expressing recombinant insulin/simian virus 40 oncogenes

TL;DR: Following the transfer into fertilized mouse eggs of recombinant genes composed of the upstream region of the rat insulin II gene linked to sequences coding for the large-T antigen of simian virus 40, large- T antigen is detected exclusively in the β-Cells of the endocrine pancreas of transgenic mice.
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