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Copyright © 2006 by the Genetics Society of America A Role for Sterol Levels in Oxygen Sensing in Saccharomyces cerevisiae Department of Molecular and Cellular Biology, Division of Genetics, Genomics, and Development, University of California, Berkeley, California 94701-3202 1Present address: Department of Medicine, Division of Cardiology, University of California, Los Angeles, CA 90095. 2Corresponding author: Department of Molecular and Cellular Biology, Division of Genetics, Genomics, and Development, 522 Barker Hall, University of California, Berkeley, CA 94701-3202. E-mail: jrine/at/berkeley.edu Communicating editor: M. Johnston Received April 26, 2006; Accepted June 4, 2006. This article has been cited by other articles in PMC.Abstract Upc2p and Ecm22p are a pair of transcription factors responsible for the basal and induced expression of genes encoding enzymes of ergosterol biosynthesis in yeast (ERG genes). Upc2p plays a second role as a regulator of hypoxically expressed genes. Both sterols and heme depend upon molecular oxygen for their synthesis, and thus the levels of both have the potential to act as indicators of the oxygen environment of cells. Hap1p is a heme-dependent transcription factor that both Upc2 and Ecm22p depend upon for basal level expression of ERG genes. However, induction of both ERG genes and the hypoxically expressed DAN/TIR genes by Upc2p and Ecm22p occurred in response to sterol depletion rather than to heme depletion. Indeed, upon sterol depletion, Upc2p no longer required Hap1p to activate ERG genes. Mot3p, a broadly acting repressor/activator protein, was previously shown to repress ERG gene expression, but the mechanism was unclear. We established that Mot3p bound directly to Ecm22p and repressed Ecm22p- but not Upc2p-mediated gene induction. |
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