Bjurström Erik Y, Lasin Praphapan, Brunnsåker Daniel, Tiukova Ievgeniia A, King Ross D
Department of Life Sciences, Chalmers University of Technology, Göteborg, Västra Götaland, Sweden.
Department of Computer Science and Engineering, Chalmers University of Technology, Göteborg, Västra Götaland, Sweden.
Yeast. 2025 Jun;42(5-7):142-156. doi: 10.1002/yea.4004. Epub 2025 Jun 26.
Tda1p is a protein kinase in Saccharomyces cerevisiae. Here we investigate the function of TDA1 during the diauxic shift using transcriptomics. We compared the gene expression in the deletion mutant tda1∆ and the reference strain (BY4741) during both the aerobic fermentation phase (log phase), and the respiratory phase (post-diauxic shift phase, PDS) in three separate independent experiments. We found: Differential gene expression analysis showed that compared to the reference strain, the tda1∆ mutant exhibited an upregulation of the glucose repressed hexose transporter HXT6 during the log phase, and upregulation of mitochondrial proteins and genes related to mitochondrial translation during the PDS phase. Gene set enrichment analysis showed an enrichment in mitochondrial translation in the PDS phase for the deletion mutant tda1∆, but not for the reference strain. Transcription factor analysis showed that the enrichment of Mig1p repressed genes was not statistically significant in TDA1 deletion mutants for neither log-phase nor PDS-phase. This conflicted with the previously suggested model that argued for an interaction between Tda1p and Mig1p. Instead, transcription factor analysis showed an enrichment of genes regulated by the HAP-complex, which regulates mitochondrial translation, during the PDS-phase in the tda1∆ mutant. The combined evidence from this study indicates that Tda1p does not participate in Mig1p-mediated glucose repression. Instead, we propose that it is involved in the regulation of mitochondrial translation by repressing the expression of HAP complex subunits.
Tda1p是酿酒酵母中的一种蛋白激酶。在此,我们利用转录组学研究了双相转变过程中TDA1的功能。在三个独立的实验中,我们比较了缺失突变体tda1∆和参考菌株(BY4741)在有氧发酵阶段(对数期)和呼吸阶段(双相转变后阶段,PDS)的基因表达。我们发现:差异基因表达分析表明,与参考菌株相比,tda1∆突变体在对数期表现出葡萄糖抑制的己糖转运蛋白HXT6上调,在PDS期线粒体蛋白和与线粒体翻译相关的基因上调。基因集富集分析表明,缺失突变体tda1∆在PDS期线粒体翻译富集,但参考菌株没有。转录因子分析表明,在TDA1缺失突变体的对数期和PDS期,Mig1p抑制基因的富集在统计学上均不显著。这与之前提出的Tda1p和Mig1p之间存在相互作用的模型相矛盾。相反,转录因子分析表明,在tda1∆突变体的PDS期,受调节线粒体翻译的HAP复合体调控的基因富集。这项研究的综合证据表明,Tda1p不参与Mig1p介导的葡萄糖抑制。相反,我们提出它通过抑制HAP复合体亚基的表达参与线粒体翻译的调控。