Dirnberger Dietmar, Seuwen Klaus
Novartis Institutes for Biomedical Research, Basel, Switzerland.
PLoS One. 2007 Sep 26;2(9):e954. doi: 10.1371/journal.pone.0000954.
Frizzled receptors have seven membrane-spanning helices and are considered as atypical G protein-coupled receptors (GPCRs). The mating response of the yeast Saccharomyces cerevisiae is mediated by a GPCR signaling system and this model organism has been used extensively in the past to study mammalian GPCR function. We show here that human Frizzled receptors (Fz1 and Fz2) can be properly targeted to the yeast plasma membrane, and that they stimulate the yeast mating pathway in the absence of added Wnt ligands, as evidenced by cell cycle arrest in G1 and reporter gene expression dependent on the mating pathway-activated FUS1 gene. Introducing intracellular portions of Frizzled receptors into the Ste2p backbone resulted in the generation of constitutively active receptor chimeras that retained mating factor responsiveness. Introducing intracellular portions of Ste2p into the Frizzled receptor backbone was found to strongly enhance mating pathway activation as compared to the native Frizzleds, likely by facilitating interaction with the yeast Galpha protein Gpa1p. Furthermore, we show reversibility of the highly penetrant G1-phase arrests exerted by the receptor chimeras by deletion of the mating pathway effector FAR1. Our data demonstrate that Frizzled receptors can functionally replace mating factor receptors in yeast and offer an experimental system to study modulators of Frizzled receptors.
卷曲受体有七个跨膜螺旋,被认为是非典型G蛋白偶联受体(GPCRs)。酿酒酵母的交配反应由一个GPCR信号系统介导,这种模式生物过去已被广泛用于研究哺乳动物GPCR的功能。我们在此表明,人类卷曲受体(Fz1和Fz2)能够正确地定位到酵母质膜上,并且在没有添加Wnt配体的情况下它们能刺激酵母交配途径,这通过G1期细胞周期停滞以及依赖于交配途径激活的FUS1基因的报告基因表达得以证明。将卷曲受体的细胞内部分引入Ste2p骨架导致产生组成型活性受体嵌合体,这些嵌合体保留了交配因子反应性。与天然卷曲受体相比,发现将Ste2p的细胞内部分引入卷曲受体骨架能强烈增强交配途径的激活,这可能是通过促进与酵母Gα蛋白Gpa1p的相互作用实现的。此外,我们通过缺失交配途径效应器FAR1证明了受体嵌合体所施加的高度穿透性G1期停滞的可逆性。我们的数据表明,卷曲受体在酵母中可以在功能上替代交配因子受体,并提供了一个研究卷曲受体调节剂的实验系统。