Davies Brandon S J, Rine Jasper
Department of Molecular and Cellular Biology, Division of Genetics, Genomics, and Development, University of California, Berkeley, California 94701-3202, USA.
Genetics. 2006 Sep;174(1):191-201. doi: 10.1534/genetics.106.059964. Epub 2006 Jun 18.
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.
Upc2p和Ecm22p是一对转录因子,负责酵母中编码麦角固醇生物合成酶的基因(ERG基因)的基础表达和诱导表达。Upc2p还作为低氧表达基因的调节因子发挥第二种作用。固醇和血红素的合成均依赖分子氧,因此二者的水平都有可能作为细胞氧环境的指标。Hap1p是一种依赖血红素的转录因子,Upc2和Ecm22p在ERG基因的基础水平表达上都依赖于它。然而,Upc2p和Ecm22p对ERG基因和低氧表达的DAN/TIR基因的诱导是对固醇耗竭而非血红素耗竭的反应。实际上,在固醇耗竭时,Upc2p不再需要Hap1p来激活ERG基因。Mot3p是一种广泛作用的阻遏物/激活蛋白,先前已证明它能抑制ERG基因表达,但其机制尚不清楚。我们确定Mot3p直接与Ecm22p结合,并抑制Ecm22p介导的基因诱导,但不抑制Upc2p介导的基因诱导。