Mazzoni Cristina, Iacchini Simone, Serafini Agnese, Falcone Claudio
Pasteur Institute-Cenci Bolognetti Foundation, Department of Cell and Developmental Biology, University of Rome La Sapienza, Rome, Italy.
FEMS Yeast Res. 2006 May;6(3):421-7. doi: 10.1111/j.1567-1364.2005.00013.x.
KlADH3 and KlADH4 are Kluyveromyces lactis genes encoding the two mitochondrial alcohol dehydrogenase activities located within mitochondria. In this yeast, ethanol induces the transcription of KlADH4 and, conversely, represses that of KlADH3. In this study, we describe the effects of the aar900 mutation on such regulation. This mutation, firstly isolated in a strain devoid of alcohol dehydrogenase genes except KlADH4, conferred to cells resistance to allyl alcohol because of the absence of the KlAdh4p activity. When the mutation was transferred by crosses to an isogenic strain containing all the alcohol dehydrogenase genes, we found that the KlADH3 gene was highly expressed even in the presence of ethanol. In addition, we observed that the absence of KlAdh4p resulted from a post-transcriptional control in that KlADH4 was transcriptionally induced by ethanol. We also found that KlPDC1, another ethanol-repressible gene, was not transcribed in the mutant in the presence of this carbon source, indicating that the escape of KlADH3 from ethanol repression was a peculiar feature of this gene. Genetic analysis showed a Mendelian segregation of the mutation that was mapped in a region of chromosome III close to the ade1 locus. Interestingly, the aar900 mutants had a pleiotropic phenotype and showed increased resistance to monovalent cations and benomyl, suggesting that the mutation could also affect genes other than the alcohol dehydrogenase ones. Strains carrying the aar900 mutation could represent useful tools to unravel the peculiar regulation of KlADH3 and KlADH4 by ethanol.
KlADH3和KlADH4是乳酸克鲁维酵母基因,编码位于线粒体内的两种线粒体乙醇脱氢酶活性。在这种酵母中,乙醇诱导KlADH4的转录,相反,抑制KlADH3的转录。在本研究中,我们描述了aar900突变对这种调控的影响。该突变最初是在一个除KlADH4外没有乙醇脱氢酶基因的菌株中分离得到的,由于缺乏KlAdh4p活性,赋予细胞对烯丙醇的抗性。当通过杂交将该突变转移到含有所有乙醇脱氢酶基因的同基因菌株中时,我们发现即使在有乙醇存在的情况下,KlADH3基因也高度表达。此外,我们观察到KlAdh4p的缺失是由转录后调控导致的,因为KlADH4在转录水平上被乙醇诱导。我们还发现,另一个受乙醇抑制的基因KlPDC1,在有这种碳源存在的情况下,在突变体中不转录,这表明KlADH3逃避乙醇抑制是该基因的一个特殊特征。遗传分析表明该突变呈现孟德尔分离,定位在第三条染色体上靠近ade1位点的区域。有趣的是,aar900突变体具有多效性表型,对单价阳离子和苯菌灵的抗性增加,这表明该突变也可能影响除乙醇脱氢酶基因以外的其他基因。携带aar900突变的菌株可能是揭示乙醇对KlADH3和KlADH4特殊调控的有用工具。