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CYB2基因表达的调控:由Hap1p、Hap2/3/4/5p和Adr1p转录因子进行转录协同调控。

Regulation of the CYB2 gene expression: transcriptional co-ordination by the Hap1p, Hap2/3/4/5p and Adr1p transcription factors.

作者信息

Ramil E, Agrimonti C, Shechter E, Gervais M, Guiard B

机构信息

Centre de Génétique Moléculaire, Laboratoire propre du CNRS associé à l'Université Pierre et Marie Curie, 91198 Gif sur Yvette, France.

出版信息

Mol Microbiol. 2000 Sep;37(5):1116-32. doi: 10.1046/j.1365-2958.2000.02065.x.

Abstract

Expression of the Saccharomyces cerevisiae nuclear gene CYB2 encoding the mitochondrial enzyme L-(+)-lactate-cytochrome c oxidoreductase (EC 1.2.2.3) is subject to several strict metabolic controls at the transcriptional level: repression due to glucose fermentation, derepression by ethanol, induction by lactate and inhibition under anaerobic conditions or in response to deficiency of haem biosynthesis. In this respect, the data obtained from the transcriptional analysis of the CYB2 gene contribute to a better understanding of the control of mitochondrial biogenesis. In this study, we show that Hap1p is the main transcriptional activator involved in the control of CYB2 transcription. We found that Hap1p activity, known to be oxygen dependent, is effected by DNA-protein interaction with two binding sites present in the CYB2 promoter. Control is moreover dependent on carbon sources. This regulation by the carbon substrates is subordinate to the activity of the complex Hap2/3/4/5p, which counteracts the negative effect of the URS1 element. Finally, our results suggest that the Adr1p transcriptional activator is also required in CYB2 transcription control. This work provides new data which allows a better understanding of the molecular mechanisms implicated in the co-regulation at the transcriptional level of the genes encoding proteins involved in various aspects of oxidative metabolism.

摘要

酿酒酵母核基因CYB2编码线粒体酶L-(+)-乳酸-细胞色素c氧化还原酶(EC 1.2.2.3),其表达在转录水平受到多种严格的代谢调控:因葡萄糖发酵而受到抑制,因乙醇而解除抑制,因乳酸而诱导表达,以及在厌氧条件下或因血红素生物合成缺陷而受到抑制。在这方面,从CYB2基因转录分析获得的数据有助于更好地理解线粒体生物发生的调控。在本研究中,我们表明Hap1p是参与CYB2转录调控的主要转录激活因子。我们发现,已知Hap1p的活性依赖于氧气,它通过与CYB2启动子中存在的两个结合位点进行DNA-蛋白质相互作用来发挥作用。此外,调控还依赖于碳源。碳底物的这种调控从属于复合物Hap2/3/4/5p的活性,该复合物可抵消URS1元件的负面影响。最后,我们的结果表明Adr1p转录激活因子在CYB2转录调控中也是必需的。这项工作提供了新的数据,有助于更好地理解在转录水平共同调控参与氧化代谢各个方面的蛋白质编码基因所涉及的分子机制。

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