Dejean Laurent, Beauvoit Bertrand, Bunoust Odile, Guérin Bernard, Rigoulet Michel
Institut de Biochimie et Génétique Cellulaires, UMR 5095 CNRS/Université Victor Segalen, 1 rue Camille Saint-Saëns, Bordeaux cedex 33077, France.
Biochem Biophys Res Commun. 2002 May 24;293(5):1383-8. doi: 10.1016/S0006-291X(02)00391-1.
We investigated the effects of genetic and physiological modulations of the cAMP-protein kinase A pathway on mitochondrial biogenesis of yeast cells grown on lactate. Yeast mutants with over-activated Ras/adenylate cyclase pathway (i.e., Ras2(val19), ira1Delta(ira2)Delta) or with a constitutive downstream activation of protein kinases A (i.e., bcyDelta) showed an increase in the mitochondrial enzyme content. In contrast, loss of Ras activity (i.e., Ras2 mutant) resulted in a slight decrease. The treatment by cAMP of a responsive mutant increased the oxidative phosphorylation capacity of cells and increased the transcript level of nuclear genes encoding for mitochondrial proteins. In contrast, the transcript level of mitochondrial DNA genes was unchanged. It is concluded that the Ras/cAMP/protein kinase A pathway is part of the regulatory circuit controlling biogenesis of the oxidative phosphorylation complexes in yeast cells.
我们研究了环磷酸腺苷-蛋白激酶A途径的基因和生理调节对在乳酸上生长的酵母细胞线粒体生物合成的影响。具有过度激活的Ras/腺苷酸环化酶途径的酵母突变体(即Ras2(val19)、ira1Delta(ira2)Delta)或具有蛋白激酶A组成型下游激活的突变体(即bcyDelta)显示线粒体酶含量增加。相反,Ras活性丧失(即Ras2突变体)导致略有下降。用环磷酸腺苷处理反应性突变体增加了细胞的氧化磷酸化能力,并增加了编码线粒体蛋白的核基因的转录水平。相反,线粒体DNA基因的转录水平没有变化。结论是,Ras/环磷酸腺苷/蛋白激酶A途径是控制酵母细胞氧化磷酸化复合物生物合成的调节回路的一部分。