Uemura H, Jigami Y
Division of Biological Chemistry, Tsukuba Research Center (MITI), Ibaraki, Japan.
Mol Cell Biol. 1992 Sep;12(9):3834-42. doi: 10.1128/mcb.12.9.3834-3842.1992.
The Saccharomyces cerevisiae GCR2 gene affects expression of most of the glycolytic genes. We report the nucleotide sequence of GCR2, which can potentially encode a 58,061-Da protein. There is a small cluster of asparagines near the center and a C-terminal region that would be highly charged but overall neutral. Fairly homologous regions were found between Gcr2 and Gcr1 proteins. To test potential interactions, the genetic method of S. Fields and O. Song (Nature [London] 340:245-246, 1989), which uses protein fusions of candidate gene products with, respectively, the N-terminal DNA-binding domain of Gal4 and the C-terminal activation domain II, assessing restoration of Gal4 function, was used. In a delta gal4 delta gal80 strain, double transformation by plasmids containing, respectively, a Gal4 (transcription-activating region)/Gcr1 fusion and a Gal4 (DNA-binding domain)/Gcr2 fusion activated lacZ expression from an integrated GAL1/lacZ fusion, indicating reconstitution of functional Gal4 through the interaction of Gcr1 and Gcr2 proteins. The Gal4 (transcription-activating region)/Gcr1 fusion protein alone complemented the defects of both gcr1 and gcr2 strains. Furthermore, a Rap1/Gcr2 fusion protein partially complemented the defects of gcr1 strains. These results suggest that Gcr2 has transcriptional activation activity and that the GCR1 and GCR2 gene products function together.
酿酒酵母GCR2基因影响大多数糖酵解基因的表达。我们报道了GCR2的核苷酸序列,它可能编码一种58,061道尔顿的蛋白质。在中心附近有一小簇天冬酰胺,还有一个C端区域,该区域电荷较高但总体呈中性。在Gcr2和Gcr1蛋白之间发现了相当同源的区域。为了测试潜在的相互作用,采用了S. Fields和O. Song(《自然》[伦敦]340:245 - 246,1989年)的遗传方法,该方法使用候选基因产物分别与Gal4的N端DNA结合结构域和C端激活结构域II的蛋白质融合体,评估Gal4功能的恢复情况。在Δgal4Δgal80菌株中,分别含有Gal4(转录激活区域)/Gcr1融合体和Gal4(DNA结合结构域)/Gcr2融合体的质粒进行双转化,激活了整合的GAL1/lacZ融合体的lacZ表达,表明通过Gcr1和Gcr2蛋白的相互作用重建了功能性Gal4。单独的Gal4(转录激活区域)/Gcr1融合蛋白弥补了gcr1和gcr2菌株的缺陷。此外,Rap1/Gcr2融合蛋白部分弥补了gcr1菌株的缺陷。这些结果表明Gcr2具有转录激活活性,并且GCR1和GCR2基因产物共同发挥作用。