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Mutational analysis of the minimal binding site of complex C1 on dps1. (A) Wild-type dps1 and mutants were used as competitors at a 200-fold molar excess in EMSAs. Dashes indicate identity with the wild-type sequence. Only the mutated bases are indicated. (B) EMSA experiment with labeled DNA probe from +1 to +90 in the absence (lane 1) or presence (lanes 2–12) of nuclear extract from rice shoots. Competitors used are indicated at the top of the gel.
