Thomas P, Davies P, Griffiths K
Biochem J. 1978 Feb 15;170(2):211-8. doi: 10.1042/bj1700211.
The kinetics of polyribonucleotide-chain elongation by rat ventral-prostate RNA polymerase B with homologous chromatin as a template were investigated. Chain elongation was measured under conditions wherein all initiation had occurred, no reinitiation took place and the reaction rate was constant. The kinetic behaviour of prostate RNA polymerase B was consistent with a mathematical model formulated for the multisubstrate enzyme. The addition of each nucleoside triphosphate was independent of the other three. The overall rate of chain elongation was lower when prostate chromatin from castrated rats was used than with prostate chromatin from normal rats. The inclusion of dihydrotestosterone-receptor complexes stimulated the rate of elongation. Androgenic effects did not appear to be directed towards the addition of individual nucleoside triphosphates, but probably towards one of the other major events in RNA-chain elongation, i.e., unwinding of DNA or movement of the enzyme along the template.
以同源染色质为模板,研究了大鼠腹侧前列腺RNA聚合酶B催化多聚核糖核苷酸链延伸的动力学。在所有起始反应均已发生、无重新起始且反应速率恒定的条件下测量链延伸。前列腺RNA聚合酶B的动力学行为与为多底物酶建立的数学模型一致。每种核苷三磷酸的添加彼此独立。与使用正常大鼠的前列腺染色质相比,使用去势大鼠的前列腺染色质时,链延伸的总体速率较低。加入二氢睾酮-受体复合物可刺激延伸速率。雄激素的作用似乎并非针对单个核苷三磷酸的添加,而是可能针对RNA链延伸中的其他主要事件之一,即DNA解旋或酶沿模板的移动。