Wolfgang W J, Hoskote A, Roberts I J, Jackson S, Forte M
Vollum Institute, L474 Oregon Health Sciences University, Portland, Oregon 97201, USA.
Genetics. 2001 Jul;158(3):1189-201. doi: 10.1093/genetics/158.3.1189.
One of the best understood signal transduction pathways activated by receptors containing seven transmembrane domains involves activation of heterotrimeric G-protein complexes containing Gs(alpha), the subsequent stimulation of adenylyl cyclase, production of cAMP, activation of protein kinase A (PKA), and the phosphorylation of substrates that control a wide variety of cellular responses. Here, we report the identification of "loss-of-function" mutations in the Drosophila Gs(alpha) gene (dgs). Seven mutants have been identified that are either complemented by transgenes representing the wild-type dgs gene or contain nucleotide sequence changes resulting in the production of altered Gs(alpha) protein. Examination of mutant alleles representing loss-of-Gs(alpha) function indicates that the phenotypes generated do not mimic those created by mutational elimination of PKA. These results are consistent with the conclusion reached in previous studies that activation of PKA, at least in these developmental contexts, does not depend on receptor-mediated increases in intracellular cAMP, in contrast to the predictions of models developed primarily on the basis of studies in cultured cells.
由含有七个跨膜结构域的受体激活的信号转导途径中,其中一条被研究得较为透彻的途径涉及激活含有Gs(α)的异源三聚体G蛋白复合物,随后刺激腺苷酸环化酶,产生环磷酸腺苷(cAMP),激活蛋白激酶A(PKA),以及对控制多种细胞反应的底物进行磷酸化。在此,我们报告了在果蝇Gs(α)基因(dgs)中“功能丧失”突变的鉴定。已鉴定出七个突变体,它们要么由代表野生型dgs基因的转基因互补,要么包含导致产生改变的Gs(α)蛋白的核苷酸序列变化。对代表Gs(α)功能丧失的突变等位基因的检查表明,所产生的表型并不模仿通过PKA的突变消除所产生的表型。这些结果与先前研究得出的结论一致,即至少在这些发育背景下,PKA的激活不依赖于受体介导的细胞内cAMP增加,这与主要基于培养细胞研究建立的模型预测相反。