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Snf1 and Cat8 are required for binding of Rds2 to the FBP1 but not the PCK1 promoter. ChIP analysis of Rds2 at the PCK1 and FBP1 promoters was performed by QPCR analysis using various strains, as indicated. Open bar, wild-type strain; black bar, Δcat8 strain; hatched bar, Δsnf1 strain. Enrichment ratios were obtained by normalizing signals to input DNA and to an untagged strain. Standard deviations are shown as vertical lines with perpendicular ends.
