Chen M Y, Long Y, Devreotes P N
Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205-2185, USA.
Genes Dev. 1997 Dec 1;11(23):3218-31. doi: 10.1101/gad.11.23.3218.
Genetic analysis was applied to identify novel genes involved in G protein-linked pathways controlling development. Using restriction enzyme-mediated integration (REMI), we have identified a new gene, Pianissimo (PiaA), involved in cAMP signaling in Dictyostelium discoideum. PiaA encodes a 130-kD cytosolic protein required for chemoattractant receptor and G protein-mediated activation of the 12 transmembrane domain adenylyl cyclase. In piaA- null mutants, neither chemoattractant stimulation of intact cells nor GTPgammaS treatment of lysates activates the enzyme; constitutive expression of PiaA reverses these defects. Cytosols of wild-type cells that contain Pia protein reconstitute the GTPgammaS stimulation of adenylyl cyclase activity in piaA- lysates, indicating that Pia is directly involved in the activation. Pia and CRAC, a previously identified cytosolic regulator, are both essential for activation of the enzyme as lysates of crac- piaA- double mutants require both proteins for reconstitution. Homologs of PiaA are found in Saccharomyces cerevisiae and Schizosaccaromyces pombe; disruption of the S. cerevisiae homolog results in lethality. We propose that homologs of Pia and similar modes of regulation of these ubiquitous G protein-linked pathways are likely to exist in higher eukaryotes.
应用遗传分析来鉴定参与控制发育的G蛋白相关信号通路的新基因。利用限制性内切酶介导的整合(REMI),我们在盘基网柄菌中鉴定出一个参与cAMP信号传导的新基因,即Pianissimo(PiaA)。PiaA编码一种130-kD的胞质蛋白,它是趋化因子受体和G蛋白介导的12跨膜结构域腺苷酸环化酶激活所必需的。在piaA基因缺失的突变体中,完整细胞的趋化因子刺激和裂解物的GTPγS处理均不能激活该酶;PiaA的组成型表达可逆转这些缺陷。含有Pia蛋白的野生型细胞的胞质溶胶可在piaA基因缺失的裂解物中重建GTPγS对腺苷酸环化酶活性的刺激作用,这表明Pia直接参与了激活过程。Pia和CRAC(一种先前鉴定的胞质调节因子)对于该酶的激活都是必不可少的,因为crac- piaA-双突变体的裂解物需要这两种蛋白才能重建活性。在酿酒酵母和粟酒裂殖酵母中发现了PiaA的同源物;酿酒酵母同源物的破坏会导致致死性。我们推测,在高等真核生物中可能存在Pia的同源物以及这些普遍存在的G蛋白相关信号通路的类似调节模式。