Thiery R, Robbins S, Khosla M, Spiegelman G B, Weeks G
Department of Microbiology, University of British Columbia, Vancouver, Canada.
Biochem Cell Biol. 1992 Oct-Nov;70(10-11):1193-9. doi: 10.1139/o92-165.
Dictyostelium discoideum contains two ras genes, rasG and rasD, that are expressed during growth and differentiation, respectively. It was shown previously that Dictyostelium transformants expressing an activated rasD gene (a mutation producing a change in amino acid 12 from glycine to threonine) developed abnormally. When developed on filters these transformants formed multitipped aggregates, which did not go on to produce final fruiting bodies, but in a submerged culture assay on a plastic surface they either formed small aggregates or did not aggregate. In this study we transformed cells with the rasG gene, mutated to change amino acid 12 from glycine to threonine. The resulting transformants developed normally on filters, but aggregation under other conditions was impaired. In particular, in submerged culture on a plastic surface they either produced very small aggregates or did not aggregate, one of the phenotypes exhibited by the activated rasD transformants. Molecular analysis of the transformants revealed the presence of high copy numbers of the mutated rasG gene, but the level of expression of the mutant gene never exceeded the level of expression of the endogenous gene. These results indicate a powerful dominant effect of a relatively small amount of the activated RasG protein in Dictyostelium.
盘基网柄菌含有两个ras基因,即rasG和rasD,它们分别在生长和分化过程中表达。先前的研究表明,表达激活型rasD基因(一种导致第12位氨基酸由甘氨酸变为苏氨酸的突变)的盘基网柄菌转化体发育异常。在滤膜上发育时,这些转化体形成多尖头聚集体,无法进一步产生最终的子实体,但在塑料表面的液体培养试验中,它们要么形成小聚集体,要么不聚集。在本研究中,我们用rasG基因转化细胞,该基因发生突变,使第12位氨基酸由甘氨酸变为苏氨酸。所得转化体在滤膜上正常发育,但在其他条件下的聚集受到损害。特别是,在塑料表面的液体培养中,它们要么产生非常小的聚集体,要么不聚集,这是激活型rasD转化体表现出的表型之一。对转化体的分子分析显示存在高拷贝数的突变rasG基因,但突变基因的表达水平从未超过内源基因的表达水平。这些结果表明,在盘基网柄菌中,相对少量的激活型RasG蛋白具有强大的显性效应。