Sánchez-Paredes Edith, Kawasaki Laura, Ongay-Larios Laura, Coria Roberto
Departamento de Genética Molecular, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Mexico.
Eukaryot Cell. 2011 Apr;10(4):540-6. doi: 10.1128/EC.00285-10. Epub 2011 Feb 18.
Yeast mating signal transduction pathways require a heterotrimeric G protein composed of Gα, Gβ, and Gγ subunits connected to a mitogen-activated protein kinase (MAPK) module. While in Saccharomyces cerevisiae elimination of Gα induces constitutive activation of the mating pathway, in Kluyveromyces lactis it produces partial sterility, which indicates that K. lactis Gα (KlGα) is required to positively activate mating. We use physical interaction experiments to determine that KlGα interacts with the adaptor protein KlSte50p. The Ras association (RA) domain of KlSte50p favored interaction with the GDP-bound KlGα subunit, and when the KlGα protein is constitutively activated, the interaction drops significantly. Additionally, KlSte50p strongly associates with the MAPK kinase kinase (MAPKKK) KlSte11p through its sterile alpha motif (SAM) domain. Genetic experiments placed KlSte50p downstream of the G protein α subunit, indicating that KlGα may stimulate the mating pathway via KlSte50p. Fusion of KlSte50p to the KlGβ subunit partially eliminated the requirement of KlGα for mating, indicating that one contribution of KlGα to the mating pathway is to facilitate plasma membrane anchoring of KlSte50p.
酵母交配信号转导途径需要一种异源三聚体G蛋白,该蛋白由与丝裂原活化蛋白激酶(MAPK)模块相连的Gα、Gβ和Gγ亚基组成。在酿酒酵母中,消除Gα会诱导交配途径的组成型激活,而在乳酸克鲁维酵母中,它会导致部分不育,这表明乳酸克鲁维酵母Gα(KlGα)对于正向激活交配是必需的。我们通过物理相互作用实验确定KlGα与衔接蛋白KlSte50p相互作用。KlSte50p的Ras关联(RA)结构域有利于与结合GDP的KlGα亚基相互作用,并且当KlGα蛋白被组成型激活时,这种相互作用会显著下降。此外,KlSte50p通过其无活性α基序(SAM)结构域与MAPK激酶激酶(MAPKKK)KlSte11p强烈结合。遗传学实验将KlSte50p置于G蛋白α亚基的下游,表明KlGα可能通过KlSte50p刺激交配途径。将KlSte50p与KlGβ亚基融合部分消除了交配对KlGα的需求,这表明KlGα对交配途径的一个作用是促进KlSte50p在质膜上的锚定。