Mulder W, Scholten I H, Grivell L A
Section for Molecular Biology, Biocentrum Amsterdam, University of Amsterdam, The Netherlands.
Mol Microbiol. 1995 Sep;17(5):813-24. doi: 10.1111/j.1365-2958.1995.mmi_17050813.x.
In Saccharomyces cerevisiae transcription of QCR8, encoding subunit VIII of the mitochondrial ubiquinol cytochrome c oxidoreductase, is subject to glucose repression, whereas in the distantly related yeast Kluyveromyces lactis it is not. The homologous promoter regions lack overall DNA-sequence identity, but do share binding sites for the transcription factors Abf1p, Cpf1p and Hap2/3/4p. For S. cerevisiae it has been established that these factors are involved in growth and carbon source control of nuclear genes encoding mitochondrial proteins. Here we present experimental evidence that K. lactis counterparts of Abf1p and Cpf1p bind independently to the KIQCR8 promoter. The presence of the KIHap2/3/4p binding site enhances binding of KIAbf1p, strongly suggesting that the KIHap2/3/4p complex stabilizes binding of KIAbf1p. In reciprocal exchanges of the QCR8 genes between S. cerevisiae and K. lactis, overall regulation of transcription was found to be species specific. In contrast to S. cerevisiae, additional elements and factors in K. lactis, distinct from Abf1p, Cpf1p and Hap2/3/4p, are able to activate transcription of the QCR8 gene during both fermentative and non-fermentative growth, as well as to induce transcription during growth on non-fermentable carbon sources. In both yeasts, Abf1p is involved in transcriptional activation under both fermentative and non-fermentative growth conditions. Hap2/3/4p plays a minor activational role during fermentative growth, but is mainly responsible for transcriptional induction under non-fermentative growth conditions. Under these latter conditions Abf1p and Hap2/3/4p activate transcription synergistically.
在酿酒酵母中,编码线粒体泛醇细胞色素c氧化还原酶亚基VIII的QCR8的转录受到葡萄糖抑制,而在远缘相关的乳酸克鲁维酵母中则不受抑制。同源启动子区域缺乏整体DNA序列同一性,但确实共享转录因子Abf1p、Cpf1p和Hap2/3/4p的结合位点。对于酿酒酵母,已经确定这些因子参与编码线粒体蛋白的核基因的生长和碳源控制。在这里,我们提供实验证据表明,Abf1p和Cpf1p的乳酸克鲁维酵母对应物独立结合到KIQCR8启动子上。KIHap2/3/4p结合位点的存在增强了KIAbf1p的结合,强烈表明KIHap2/3/4p复合物稳定了KIAbf1p的结合。在酿酒酵母和乳酸克鲁维酵母之间对QCR8基因进行相互交换时,发现转录的整体调控具有物种特异性。与酿酒酵母不同,乳酸克鲁维酵母中除Abf1p、Cpf1p和Hap2/3/4p之外的其他元件和因子,能够在发酵和非发酵生长过程中激活QCR8基因的转录,以及在不可发酵碳源上生长期间诱导转录。在两种酵母中,Abf1p在发酵和非发酵生长条件下均参与转录激活。Hap2/3/4p在发酵生长期间起次要的激活作用,但主要负责非发酵生长条件下的转录诱导。在后一种条件下,Abf1p和Hap2/3/4p协同激活转录。