Jelicić Branka, Traven Ana, Filić Vedrana, Sopta Mary
Department of Molecular Biology, Ruder Bosković Institute, Bijenicka 54, 10000 Zagreb, Croatia.
FEMS Microbiol Lett. 2005 Dec 15;253(2):207-13. doi: 10.1016/j.femsle.2005.09.033. Epub 2005 Oct 7.
Mitochondrial dysfunction has been shown to elicit broad effects on nuclear gene expression. We show here that transcription dependent on the prototypical acidic activator Gal4 is responsive to mitochondrial dysfunction. In cells with no mitochondrial DNA, Gal4-dependent gene expression is elevated. A minimal Gal4 activator containing the DNA binding and activation domain is sufficient for this response. Transcription dependent on a fusion of Gal4 to a heterologous DNA binding domain is similarly elevated in a mitochondrial mutant. Analysis of different Gal4-dependent promoters and gel mobility shift assays suggest that the effect of mitochondrial dysfunction on Gal4 activity is related to increased DNA binding to the cognate Gal4 element. Given that fermentation is the only means to obtain energy in respiratory deficient cells, it is possible that higher Gal4 activity in cells with dysfunctional mitochondria works to promote more efficient fermentation of galactose.
线粒体功能障碍已被证明会对核基因表达产生广泛影响。我们在此表明,依赖于典型酸性激活剂Gal4的转录对线粒体功能障碍有反应。在没有线粒体DNA的细胞中,Gal4依赖的基因表达会升高。一个包含DNA结合和激活结构域的最小Gal4激活剂足以产生这种反应。在一个线粒体突变体中,依赖于Gal4与异源DNA结合结构域融合的转录同样会升高。对不同Gal4依赖启动子的分析和凝胶迁移率变动分析表明,线粒体功能障碍对Gal4活性的影响与DNA与同源Gal4元件的结合增加有关。鉴于发酵是呼吸缺陷细胞中获取能量的唯一途径,线粒体功能异常的细胞中较高的Gal4活性可能有助于促进半乳糖更有效的发酵。