Ye Tian, García-Salcedo Raúl, Ramos José, Hohmann Stefan
Department of Cell and Molecular Biology/Microbiology, Göteborg University, Box 462, S-40530 Göteborg, Sweden.
Eukaryot Cell. 2006 Oct;5(10):1611-21. doi: 10.1128/EC.00215-06.
Gis4 is a new component of the system required for acquisition of salt tolerance in Saccharomyces cerevisiae. The gis4Delta mutant is sensitive to Na(+) and Li(+) ions but not to osmotic stress. Genetic evidence suggests that Gis4 mediates its function in salt tolerance, at least partly, together with the Snf1 protein kinase and in parallel with the calcineurin protein phosphatase. When exposed to salt stress, mutants lacking gis4Delta display a defect in maintaining low intracellular levels of Na(+) and Li(+) ions and exporting those ions from the cell. This defect is due to diminished expression of the ENA1 gene, which encodes the Na(+) and Li(+) export pump. The protein sequence of Gis4 is poorly conserved and does not reveal any hints to its molecular function. Gis4 is enriched at the cell surface, probably due to C-terminal farnesylation. The CAAX box at the C terminus is required for cell surface localization but does not seem to be strictly essential for the function of Gis4 in salt tolerance. Gis4 and Snf1 seem to share functions in the control of ion homeostasis and ENA1 expression but not in glucose derepression, the best known role of Snf1. Together with additional evidence that links Gis4 genetically and physically to Snf1, it appears that Gis4 may function in a pathway in which Snf1 plays a specific role in controlling ion homeostasis. Hence, it appears that the conserved Snf1 kinase plays roles in different pathways controlling nutrient as well as stress response.
Gis4是酿酒酵母获得耐盐性所需系统的一个新组分。gis4Delta突变体对Na(+)和Li(+)离子敏感,但对渗透胁迫不敏感。遗传学证据表明,Gis4至少部分地与Snf1蛋白激酶一起并与钙调神经磷酸酶平行介导其在耐盐性中的功能。当暴露于盐胁迫时,缺乏gis4Delta的突变体在维持细胞内低水平的Na(+)和Li(+)离子以及将这些离子从细胞中输出方面存在缺陷。这种缺陷是由于编码Na(+)和Li(+)输出泵的ENA1基因表达减少所致。Gis4的蛋白质序列保守性较差,没有揭示其分子功能的任何线索。Gis4在细胞表面富集,可能是由于C末端法尼基化。C末端的CAAX框是细胞表面定位所必需的,但似乎对于Gis4在耐盐性中的功能不是严格必需的。Gis4和Snf1似乎在离子稳态和ENA1表达的控制中共享功能,但在葡萄糖去阻遏(Snf1最知名的作用)方面没有共享功能。连同将Gis4与Snf1在遗传和物理上联系起来的其他证据,似乎Gis4可能在Snf1在控制离子稳态中起特定作用的途径中发挥作用。因此,似乎保守的Snf1激酶在控制营养以及应激反应的不同途径中发挥作用。