Lam Mandy Hiu Yi, Snider Jamie, Rehal Monique, Wong Victoria, Aboualizadeh Farzaneh, Drecun Luka, Wong Olivia, Jubran Bellal, Li Meirui, Ali Mehrab, Jessulat Matthew, Deineko Viktor, Miller Rachel, Lee Mid eum, Park Hay-Oak, Davidson Alan, Babu Mohan, Stagljar Igor
Donnelly Centre, University of Toronto, 160 College Street, Toronto, ON M5S 3E1, Canada.
Donnelly Centre, University of Toronto, 160 College Street, Toronto, ON M5S 3E1, Canada; Department of Biochemistry, University of Toronto, Medical Science Building, 1 King's College Circle, Toronto, ON M5S 1A8, Canada.
J Mol Biol. 2015 Jun 5;427(11):2088-103. doi: 10.1016/j.jmb.2015.01.016. Epub 2015 Jan 30.
Sho1p, an integral membrane protein, plays a vital role in the high-osmolarity glycerol (HOG) mitogen-activated protein kinase pathway in the yeast Saccharomyces cerevisiae. Activated under conditions of high osmotic stress, it interacts with other HOG pathway proteins to mediate cell signaling events, ensuring that yeast cells can adapt and remain viable. In an attempt to further understand how the function of Sho1p is regulated through its protein-protein interactions (PPIs), we identified 49 unique Sho1p PPIs through the use of membrane yeast two-hybrid (MYTH), an assay specifically suited to identify PPIs of full-length integral membrane proteins in their native membrane environment. Secondary validation by literature search, or two complementary PPI assays, confirmed 80% of these interactions, resulting in a high-quality Sho1p interactome. This set of putative PPIs included both previously characterized interactors, along with a large subset of interactors that have not been previously identified as binding to Sho1p. The SH3 domain of Sho1p was found to be important for binding to many of these interactors. One particular novel interactor of interest is the glycerol transporter Fps1p, which was shown to require the SH3 domain of Sho1p for binding via its N-terminal soluble regulatory domain. Furthermore, we found that Fps1p is involved in the positive regulation of Sho1p function and plays a role in the phosphorylation of the downstream kinase Hog1p. This study represents the largest membrane interactome analysis of Sho1p to date and complements past studies on the HOG pathway by increasing our understanding of Sho1p regulation.
Sho1p是一种整合膜蛋白,在酿酒酵母的高渗甘油(HOG)丝裂原活化蛋白激酶途径中发挥着至关重要的作用。在高渗胁迫条件下被激活后,它与其他HOG途径蛋白相互作用,介导细胞信号转导事件,确保酵母细胞能够适应并保持活力。为了进一步了解Sho1p的功能是如何通过其蛋白质-蛋白质相互作用(PPI)进行调节的,我们通过使用膜酵母双杂交(MYTH)鉴定了49种独特的Sho1p PPI,这是一种特别适合于在其天然膜环境中鉴定全长整合膜蛋白PPI的检测方法。通过文献检索或两种互补的PPI检测进行的二次验证,证实了其中80%的相互作用,从而得到了一个高质量的Sho1p相互作用组。这组推定的PPI既包括先前已鉴定的相互作用蛋白,也包括一大类先前未被鉴定为与Sho1p结合的相互作用蛋白。发现Sho1p的SH3结构域对于与许多这些相互作用蛋白的结合很重要。一个特别有趣的新型相互作用蛋白是甘油转运蛋白Fps1p,它通过其N端可溶性调节结构域与Sho1p的SH3结构域结合。此外,我们发现Fps1p参与Sho1p功能的正向调节,并在下游激酶Hog1p的磷酸化中发挥作用。这项研究是迄今为止对Sho1p进行的最大规模的膜相互作用组分析,通过增进我们对Sho1p调节的理解,补充了过去对HOG途径的研究。