Breus Oksana, Panasyuk Ganna, Gout Ivan T, Filonenko Valeriy, Nemazanyy Ivan
Department of Cell Signalling, Institute of Molecular Biology and Genetics National Academy of Sciences of Ukraine, Kyiv, Ukraine.
Biochem Biophys Res Commun. 2009 Aug 7;385(4):581-5. doi: 10.1016/j.bbrc.2009.05.102. Epub 2009 May 29.
The complex interplay between cellular signaling and metabolism in eukaryotic cells just start to emerge. Coenzyme A (CoA) and its derivatives play a key role in cell metabolism and also participate in regulatory processes. CoA synthase (CoASy) is a mitochondria-associated enzyme which mediates two final stages of de novo CoA biosynthesis. Here, we report that CoASy is involved in signaling events in the cell and forms a functional complex with p85alphaPI3K in vivo. Importantly, observed interaction of endogenous CoASy and p85alphaPI3K is regulated in a growth factor dependent manner. Surprisingly, both catalytic p110alpha and regulatory p85alpha subunits of PI3K were detected in mitochondrial fraction where mitochondria-localized p85alphaPI3K was found in complex with CoASy. Unexpectedly, significant changes of PI3K signaling pathway activity were observed in experiments with siRNA-mediated CoASy knockdown pointing on the role of CoA biosynthetic pathway in signal transduction.
真核细胞中细胞信号传导与代谢之间复杂的相互作用才刚刚开始显现。辅酶A(CoA)及其衍生物在细胞代谢中起关键作用,并且也参与调节过程。辅酶A合酶(CoASy)是一种与线粒体相关的酶,它介导从头合成CoA的两个最终阶段。在此,我们报道CoASy参与细胞中的信号事件,并在体内与p85αPI3K形成功能复合物。重要的是,观察到内源性CoASy与p85αPI3K的相互作用以生长因子依赖性方式受到调节。令人惊讶的是,在与CoASy结合的线粒体定位的p85αPI3K所在的线粒体部分中检测到了PI3K的催化性p110α和调节性p85α亚基。出乎意料的是,在用siRNA介导的CoASy敲低实验中观察到PI3K信号通路活性发生了显著变化,这表明CoA生物合成途径在信号转导中的作用。