Abstract
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. The feasibility of the technique was verified by selecting DNA fragments that contained binding sites for GCN4, a well-characterized yeast transcriptional activator. The DNA binding domain of NGFI-B, expressed as part of a LexA-NGFI-B-GAL4 chimeric activator, was then used to isolate a rat genomic DNA fragment that contained an NGFI-B binding site. The NGFI-B response element (NBRE) is similar to but functionally distinct from elements recognized by the estrogen and thyroid hormone receptors and the hormone receptor-like proteins COUP-TF, CF1, and H-2RIIBP. Cotransfection experiments in mammalian cells demonstrated that NGFI-B can activate transcription from the NBRE with or without its putative ligand binding domain.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Bacterial Proteins / metabolism
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Base Sequence
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Binding Sites
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Cloning, Molecular
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DNA, Fungal / metabolism*
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / metabolism*
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DNA-Binding Proteins / pharmacology
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Fungal Proteins / metabolism
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Molecular Sequence Data
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Nuclear Receptor Subfamily 4, Group A, Member 1
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Plasmids
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Protein Kinases*
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Rats
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Receptors, Cytoplasmic and Nuclear
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Receptors, Steroid
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Repressor Proteins
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Saccharomyces cerevisiae / genetics*
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Saccharomyces cerevisiae Proteins*
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Serine Endopeptidases*
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Transcription Factors / genetics
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Transcription Factors / metabolism*
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Transcription Factors / pharmacology
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Transcription, Genetic
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Transfection
Substances
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Bacterial Proteins
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DNA, Fungal
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DNA-Binding Proteins
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Fungal Proteins
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GAL4 protein, S cerevisiae
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LexA protein, Bacteria
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Nr4a1 protein, rat
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Nuclear Receptor Subfamily 4, Group A, Member 1
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Receptors, Cytoplasmic and Nuclear
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Receptors, Steroid
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Repressor Proteins
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Saccharomyces cerevisiae Proteins
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Transcription Factors
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Protein Kinases
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Serine Endopeptidases