Watanabe D, Abe M, Ohya Y
Department of Integrated Biosciences, Graduate School of Frontier Science, University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Yeast. 2001 Jul;18(10):943-51. doi: 10.1002/yea.742.
Selection of an extragenic suppressor of fks1-1154 Deltafks2, mutations in the catalytic subunits of yeast 1,3-beta-glucan synthase (GS) conferring temperature-sensitivity, led to the LRG1 gene, which was originally identified as a LIM-RhoGAP homologous gene. Mutations in the LRG1 gene restore impaired 1,3-beta-glucan synthesis in the fks1-1154 Deltafks2 mutant as well as that in rho1-2, a temperature-sensitive mutant of Rho-type GTPase that functions as a regulatory subunit of GS. Two-hybrid analyses of Lrg1p, which contains a sequence conserved among Rho GTPase-activating proteins (GAPs), revealed its specific interactions with the active form of Rho1p. Among eight potential yeast RhoGAPs, Lrg1p is the only member that negatively regulates GS activity: mutations in the rest of GAPs, including bem2, Deltabem3, Deltasac7, Deltabag7, Deltarga1, Deltarga2 and Deltargd1, do not suppress impairment of 1,3-beta-glucan synthesis. Analyses of Mpk1p phosphorylation revealed the inability of Lrg1p to regulate the Pkc1p-MAP kinase cascade, a distinct Rho1p-regulating signalling pathway known to be affected by the GAPs, Bem2p and Sac7p. Thus, different groups of Rho1p GAPs control the activity of different Rho1p-effector proteins.
酵母1,3-β-葡聚糖合酶(GS)催化亚基中的fks1-1154Δfks2突变赋予温度敏感性,对其一个基因外抑制子的筛选得到了LRG1基因,该基因最初被鉴定为一个LIM-RhoGAP同源基因。LRG1基因突变可恢复fks1-1154Δfks2突变体以及rho1-2(一种作为GS调节亚基的Rho型GTP酶的温度敏感突变体)中受损的1,3-β-葡聚糖合成。对含有Rho GTP酶激活蛋白(GAPs)中保守序列的Lrg1p进行的双杂交分析,揭示了它与Rho1p活性形式的特异性相互作用。在八个潜在的酵母RhoGAP中,Lrg1p是唯一负调节GS活性的成员:包括bem2、Δbem3、Δsac7、Δbag7、Δraga1、Δraga2和Δrgd1在内的其他GAPs突变均不能抑制1,3-β-葡聚糖合成的损伤。对Mpk1p磷酸化的分析表明,Lrg1p无法调节Pkc1p-MAP激酶级联反应,这是一条已知受GAPs、Bem2p和Sac7p影响的独特的Rho1p调节信号通路。因此,不同组的Rho1p GAPs控制不同Rho1p效应蛋白的活性。