Publication | Closed Access
Cooperative DNA Binding and Sequence-Selective Recognition Conferred by the STAT Amino-Terminal Domain
480
Citations
22
References
1996
Year
Structural BioinformaticsGeneticsSignal RecognitionMolecular BiologyMolecular GeneticsGene Regulatory NetworkSequence MotifTranscriptional RegulationStat BindingGene StructureStat ProteinsDna ReplicationSequence-selective Recognition ConferredGene ExpressionFunctional GenomicsBioinformaticsStructural BiologyTranscription RegulationSignal TransductionNatural SciencesGene RegulationSystems BiologyMedicineStat Amino-terminal DomainCooperative Dna Binding
STAT proteins (signal transducers and activators of transcription) activate distinct target genes despite having similar DNA binding preferences. The transcriptional specificity of STAT proteins was investigated on natural STAT binding sites near the interferon-gamma gene. These sites are arranged in multiple copies and required cooperative interactions for STAT binding. The conserved amino-terminal domain of STAT proteins was required for cooperative DNA binding, although this domain was not essential for dimerization or binding to a single site. Cooperative binding interactions enabled the STAT proteins to recognize variations of the consensus site. These sites can be specific for the different STAT proteins and may function to direct selective transcriptional activation.
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