Sekito Takayuki, Liu Zhengchang, Thornton Janet, Butow Ronald A
Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9148, USA.
Mol Biol Cell. 2002 Mar;13(3):795-804. doi: 10.1091/mbc.01-09-0473.
An important function of the RTG signaling pathway is maintenance of intracellular glutamate supplies in yeast cells with dysfunctional mitochondria. Herein, we report that MKS1 is a negative regulator of the RTG pathway, acting between Rtg2p, a proximal sensor of mitochondrial function, and the bHLH transcription factors Rtg1p and Rtg3p. In mks1 Delta cells, RTG target gene expression is constitutive, bypassing the requirement for Rtg2p, and is no longer repressible by glutamate. We show further that Mks1p is a phosphoprotein whose phosphorylation pattern parallels that of Rtg3p in response to activation of the RTG pathway, and that Mks1p is in a complex with Rtg2p. MKS1 was previously implicated in the formation of [URE3], an inactive prion form of a negative regulator of the nitrogen catabolite repression pathway, Ure2p. rtg Delta mutations induce [URE3] and can do so independently of MKS1. We find that glutamate suppresses [URE3] formation, suggesting that the Mks1p effect on the formation of [URE3] can occur indirectly via regulation of the RTG pathway.
在酵母细胞中,线粒体功能失调时,RTG信号通路的一个重要功能是维持细胞内谷氨酸的供应。在此,我们报告MKS1是RTG通路的负调控因子,作用于线粒体功能的近端传感器Rtg2p与bHLH转录因子Rtg1p和Rtg3p之间。在mks1Δ细胞中,RTG靶基因的表达是组成型的,绕过了对Rtg2p的需求,并且不再受谷氨酸抑制。我们进一步表明,Mks1p是一种磷蛋白,其磷酸化模式与RTG通路激活时Rtg3p的磷酸化模式相似,并且Mks1p与Rtg2p形成复合物。MKS1以前被认为与[URE3]的形成有关,[URE3]是氮分解代谢物阻遏途径的负调控因子Ure2p的一种无活性的朊病毒形式。rtgΔ突变会诱导[URE3]的形成,并且可以独立于MKS1进行。我们发现谷氨酸会抑制[URE3]的形成,这表明Mks1p对[URE3]形成的影响可能通过调节RTG通路间接发生。