Table 1.

Summary of oligonucleotides for gel shifts and mutagenesis

OligonucleotideSequence
FPA (−3994 to −3967) GCTGGAACCCGGGGCGGGCGGGCTCAGG 
FPA-GC-g mt GCTGGAACCCGGGGCtGtCGGGCTCAGG  
FPB (−3957 to −3933) AGGCGGGGGAGGGGGCGGCGACCCG 
FPB-GC-f mt AGGCGGGGGAtGGttCGGCGACCCG  
FPC (−3876 to −3845) CATGCCGGGGTCCCGGGGAGGGCGGGGGTCGG 
FPD (−3816 to −3787) GGGTGGGGAAGGGGTGGGGGGGAGGGGCCC  
FPD-GT-d mt GGGTGGGGAAGGGtTGGGGGGGAGGGGCCC 
−3766/−3725 GGGGCTGGGCGGGCGGGTGCTCTGCCACGAGACATTGGCCG 
USF-1 mt GGGGCTGGGCGGGCGGGTGCTCTGCCAtcAGACATTGGCCG 
−3724/−3682 CGCCGGCCTCCGCCCCCGCCTCTCCGCCAATCACCGCCCGCCT 
NF-Y mt CGCCGGCCTCCGCCCCCGCCTCTCCGCtAtTCACCGCCCGCCT 
OligonucleotideSequence
FPA (−3994 to −3967) GCTGGAACCCGGGGCGGGCGGGCTCAGG 
FPA-GC-g mt GCTGGAACCCGGGGCtGtCGGGCTCAGG  
FPB (−3957 to −3933) AGGCGGGGGAGGGGGCGGCGACCCG 
FPB-GC-f mt AGGCGGGGGAtGGttCGGCGACCCG  
FPC (−3876 to −3845) CATGCCGGGGTCCCGGGGAGGGCGGGGGTCGG 
FPD (−3816 to −3787) GGGTGGGGAAGGGGTGGGGGGGAGGGGCCC  
FPD-GT-d mt GGGTGGGGAAGGGtTGGGGGGGAGGGGCCC 
−3766/−3725 GGGGCTGGGCGGGCGGGTGCTCTGCCACGAGACATTGGCCG 
USF-1 mt GGGGCTGGGCGGGCGGGTGCTCTGCCAtcAGACATTGGCCG 
−3724/−3682 CGCCGGCCTCCGCCCCCGCCTCTCCGCCAATCACCGCCCGCCT 
NF-Y mt CGCCGGCCTCCGCCCCCGCCTCTCCGCtAtTCACCGCCCGCCT 

DNA sequences for wild-type double-stranded oligonucleotides were used as probes or competitive oligonucleotides in gel shift assays. Single-stranded mutant oligonucleotides were used in the preparation of mutant reporter gene constructs for transient transfection experiments. The consensus sequences of the GC/GT-box, E-box, and CAAT-box elements are underlined. Lowercase letters indicate the bases mutated.

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