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ROM7/BEM4编码一种与酿酒酵母中的Rho1p小GTP结合蛋白相互作用的新型蛋白质。

ROM7/BEM4 encodes a novel protein that interacts with the Rho1p small GTP-binding protein in Saccharomyces cerevisiae.

作者信息

Hirano H, Tanaka K, Ozaki K, Imamura H, Kohno H, Hihara T, Kameyama T, Hotta K, Arisawa M, Watanabe T, Qadota H, Ohya Y, Takai Y

机构信息

Department of Molecular Biology and Biochemistry, Osaka University Medical School, Japan.

出版信息

Mol Cell Biol. 1996 Aug;16(8):4396-403. doi: 10.1128/MCB.16.8.4396.

Abstract

The RHO1 gene encodes a homolog of the mammalian RhoA small GTP-binding protein in the yeast Saccharomyces cerevisiae. Rho1p is localized at the growth site and is required for bud formation. The RHO1(G22S, D125N) mutation is a temperature-sensitive and dominant negative mutation of RHO1, and a multicopy suppressor of RHO1(G22S, D125N), ROM7, was isolated. Nucleotide sequencing of ROM7 revealed that it is identical to the BEM4 gene (GenBank accession number L27816), although its physiological function has not yet been reported. Disruption of BEM4 resulted in the cold- and temperature-sensitive growth phenotypes, and cells of the deltabem4 mutant showed abnormal morphology, suggesting that BEM4 is involved in the budding process. The temperature-sensitive growth phenotype was suppressed by overexpression of RHO1, ROM2, which encodes a Rho1p-specific GDP/GTP exchange factor, or PKC1, which encodes a target of Rho1p. Moreover, glucan synthase activity, which is activated by Rho1p, was significantly reduced in the deltabem4 mutant. Two-hybrid and biochemical experiments revealed that Bem4p directly interacts with the nucleotide-free form of Rho1p and, to lesser extents, with the GDP- and GTP-bound forms of Rho1p, although Bem4p showed neither GDP/GTP exchange factor, GDP dissociation inhibitor, nor GTPase-activating protein activity toward Rho1p. These results indicate that Bem4p is a novel protein directly interacting with Rho1p and is involved in the RHO1-mediated signaling pathway.

摘要

RHO1基因在酿酒酵母中编码与哺乳动物RhoA小GTP结合蛋白同源的蛋白。Rho1p定位于生长位点,是芽形成所必需的。RHO1(G22S, D125N)突变是RHO1的温度敏感型显性负突变,并且分离出了RHO1(G22S, D125N)的多拷贝抑制子ROM7。ROM7的核苷酸测序表明它与BEM4基因相同(GenBank登录号L27816),尽管其生理功能尚未见报道。BEM4的缺失导致了冷敏感和温度敏感的生长表型,并且deltabem4突变体的细胞表现出异常形态,这表明BEM4参与芽殖过程。RHO1、编码Rho1p特异性GDP/GTP交换因子的ROM2或编码Rho1p靶标的PKC1的过表达抑制了温度敏感型生长表型。此外,在deltabem4突变体中,由Rho1p激活的葡聚糖合酶活性显著降低。双杂交和生化实验表明,Bem4p直接与无核苷酸形式的Rho1p相互作用,并且在较小程度上与GDP结合形式和GTP结合形式的Rho1p相互作用,尽管Bem4p对Rho1p既不表现出GDP/GTP交换因子活性、GDP解离抑制活性,也不表现出GTP酶激活蛋白活性。这些结果表明Bem4p是一种直接与Rho1p相互作用的新型蛋白,并且参与RHO1介导的信号通路。

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