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A schematic representation of the ICP0 promoter/reporter gene constructs used to generate reporter mutants. Binding sites for factors shown to influence ICP0 promoter function in transient transfection assays in tissue culture cells are indicated. Question marks denote potential TAATGRAT sequences, Octa protein binding sites (Oct), or factor binding sequences similar to those shown to be functional in a more proximal promoter region in vitro.
