Manen C, Russel D H
Science. 1977 Feb 4;195(4277):505-6. doi: 10.1126/science.835013.
Reparts suggest that the activity of RNA polymerase I is modulated by a labile protein with a hlaf-life of 10 to 20 minutes. Ornithine decarboxylase is the only labile protein (half-life, 10 to 20 minutes) that increases in activity prior to increased RNA polymerase I activity. The addition of a small amount of a highly purified ornithine decarboxylase preparation to an RNA polymerase I assay increases the initial rate of the reaction as well as the time for which the assay is linear. The incorporation patterns of 14C-labeled adenosine triphosphate and 32P-labeled adenosine triphosphate into RNA indicate that the addition of ornithine decarboxylase to the RNA polymerase assay increases the rate of initiation. This report demonstrates a novel way to purify ornithine decarboxylase by RNA polymerase I affinity chromatography and presents data in support of the hypothesis that the labile protein which modulates RNA polymerase I activity is ornithine decarboxylase.
报告表明,RNA聚合酶I的活性受一种半衰期为10至20分钟的不稳定蛋白质调节。鸟氨酸脱羧酶是唯一一种半衰期为10至20分钟且在RNA聚合酶I活性增加之前活性就升高的不稳定蛋白质。向RNA聚合酶I测定中添加少量高度纯化的鸟氨酸脱羧酶制剂,可提高反应的初始速率以及测定呈线性的时间。14C标记的三磷酸腺苷和32P标记的三磷酸腺苷掺入RNA的模式表明,向RNA聚合酶测定中添加鸟氨酸脱羧酶可提高起始速率。本报告展示了一种通过RNA聚合酶I亲和色谱法纯化鸟氨酸脱羧酶的新方法,并提供数据支持调节RNA聚合酶I活性的不稳定蛋白质是鸟氨酸脱羧酶这一假说。