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J Biol Chem ; 269(32): 20340-6, 1994 Aug 12.
Article in English | MEDLINE | ID: mdl-8051128

ABSTRACT

NF-Y is a highly conserved heteromeric CCAAT-binding transcription factor involved in the function of several promoters. The NF-YA subunit contains a domain of high homology to yeast HAP2, which we show to be necessary and sufficient to mediate interactions with the NF-YB subunit and with DNA. Using protein affinity columns derivatized with amino acid substitution mutants, we further dissect this region into two functionally separable subdomains. The subunit association function resides in a 21-amino acid stretch, which is almost perfectly conserved among different species, while interaction with DNA resides in another short segment. We also show that DNA-binding mutants act as dominant repressors of NF-Y-DNA complex formation and of NF-Y-dependent transcription.


Subject(s)
DNA-Binding Proteins/genetics , Genes, Dominant , Transcription Factors/genetics , Amino Acid Sequence , Base Sequence , CCAAT-Enhancer-Binding Proteins , DNA/metabolism , DNA-Binding Proteins/metabolism , Molecular Sequence Data , Mutation , Nuclear Proteins/metabolism , Oligodeoxyribonucleotides , Sequence Alignment , Structure-Activity Relationship , Transcription Factors/metabolism
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