(11,15,32,39). Most significantly, investigations into its regulation have been driven by the fact that altered INO1 expression is a hallmark of general defects in transcription (35). This study is significant because it reports novel findings regarding new regulators of INO1 transcription.The mechanism for the derepression of INO1 transcription has been extensively studied. Derepression requires the basic helixloop-helix (bHLH) transcription factors Ino2p and Ino4p that bind as a heterodimer to two cis-regulatory (UAS INO ) elements in the INO1 promoter (Fig. 1) (2, 6, 55, 67, 73). The Ino2p activation domain then recruits the Snf1p histone kinase to the INO1 promoter, which phosphorylates Ser10 of histone H3 (62). Phosphorylated histone H3 serves as a docking site for the SAGA acetyltransferase, which acetylates Lys14 on histone H3, but also recruits the TATA-binding protein (TBP) (Fig. 1)