Chen G C, Kim Y J, Chan C S
Department of Microbiology, The University of Texas, Austin, Texas 78712, USA.
Genes Dev. 1997 Nov 15;11(22):2958-71. doi: 10.1101/gad.11.22.2958.
BEM2 of Saccharomyces cerevisiae encodes a Rho-type GTPase-activating protein that is required for proper bud site selection at 26 degrees C and for bud emergence at elevated temperatures. We show here that the temperature-sensitive growth phenotype of bem2 mutant cells can be suppressed by increased dosage of the GIC1 gene. The Gic1 protein, together with its structural homolog Gic2, are required for cell size and shape control, bud site selection, bud emergence, actin cytoskeletal organization, mitotic spindle orientation/positioning, and mating projection formation in response to mating pheromone. Each protein contains a CRIB (Cdc42/Rac-interactive binding) motif and each interacts in the two-hybrid assay with the GTP-bound form of the Rho-type Cdc42 GTPase, a key regulator of polarized growth in yeast. The CRIB motif of Gic1 and the effector domain of Cdc42 are required for this association. Genetic experiments indicate that Gic1 and Gic2 play positive roles in the Cdc42 signal transduction pathway, probably as effectors of Cdc42. Subcellular localization studies with a functional green fluorescent protein-Gic1 fusion protein indicate that this protein is concentrated at the incipient bud site of unbudded cells, at the bud tip and mother-bud neck of budded cells, and at cortical sites on large-budded cells that may delimit future bud sites in the two progeny cells. The ability of Gic1 to associate with Cdc42 is important for its function but is apparently not essential for its subcellular localization.
酿酒酵母的BEM2编码一种Rho型GTP酶激活蛋白,该蛋白在26摄氏度时对正确的芽位选择以及在高温时对芽的出现是必需的。我们在此表明,bem2突变细胞的温度敏感生长表型可通过增加GIC1基因的剂量来抑制。Gic1蛋白与其结构同源物Gic2一起,对于细胞大小和形状控制、芽位选择、芽的出现、肌动蛋白细胞骨架组织、有丝分裂纺锤体定向/定位以及响应交配信息素形成交配突起是必需的。每种蛋白都包含一个CRIB(Cdc42/Rac相互作用结合)基序,并且在双杂交试验中每种蛋白都与Rho型Cdc42 GTP酶的GTP结合形式相互作用,Rho型Cdc42 GTP酶是酵母中极化生长的关键调节因子。Gic1的CRIB基序和Cdc42的效应结构域对于这种关联是必需的。遗传实验表明,Gic1和Gic2在Cdc42信号转导途径中起积极作用,可能作为Cdc42的效应器。对功能性绿色荧光蛋白 - Gic1融合蛋白的亚细胞定位研究表明,该蛋白集中在未出芽细胞的初始芽位、出芽细胞的芽尖和母 - 芽颈部,以及大芽细胞的皮质位点,这些位点可能界定两个子代细胞中未来的芽位。Gic1与Cdc42结合的能力对其功能很重要,但显然对其亚细胞定位不是必需的。