Urata M, Suzuki N, Hosoya T
Biochem J. 1987 Jan 1;241(1):169-74. doi: 10.1042/bj2410169.
In order to examine the relationship between RNA polymerase I and ornithine decarboxylase (ODC), three lines of experiments were performed, with the following results. The glucocorticoid-induced increase of RNA polymerase I in rat liver nuclei was not abolished by administration of inhibitors of ODC synthesis and activity, namely 1,3-diaminopropane and 2-difluoromethylornithine respectively. Anti-ODC antibody did not cross-react with RNA polymerase I solubilized from rat liver nucleoli, indicating the absence of a common protein sequence in these enzymes. The ODC preparation which was treated with transglutaminase in the presence of putrescine could not stimulate the activity of RNA polymerase I in nuclei of liver and prostate. All these results suggest that the increases in ODC protein or activity are not a prerequisite to the increase in RNA polymerase I after hormonal or physiological stimuli, but rather that the increases in both enzymes are separate responses to the primary stimuli.
为了研究RNA聚合酶I与鸟氨酸脱羧酶(ODC)之间的关系,进行了三组实验,结果如下。给予ODC合成抑制剂1,3 - 二氨基丙烷和活性抑制剂2 - 二氟甲基鸟氨酸,均未消除糖皮质激素诱导的大鼠肝细胞核中RNA聚合酶I的增加。抗ODC抗体与从大鼠肝核仁中溶解的RNA聚合酶I没有交叉反应,表明这些酶中不存在共同的蛋白质序列。在腐胺存在下用转谷氨酰胺酶处理的ODC制剂不能刺激肝和前列腺细胞核中RNA聚合酶I的活性。所有这些结果表明,在激素或生理刺激后,ODC蛋白或活性的增加并非RNA聚合酶I增加的先决条件,而是这两种酶的增加是对主要刺激的独立反应。