Schumm D E, Richter R
J Neurochem. 1982 Apr;38(4):925-30. doi: 10.1111/j.1471-4159.1982.tb05331.x.
The poly(adenylate)[poly(A)] polymerase of rat brain, as in rat liver, is located primarily in the nuclear sap when nuclei are prepared under hypertonic conditions. The enzyme can be released from nuclei in two forms. Form I is prepared by gentle incubation of nuclei at 0 degrees C in hypotonic buffer. It has a Mn optimum of 0.6 mM and a pH optimum between 8 and 9. The ATP concentration curve plateaus at 0.2 mM. The optimal poly(A) primer concentration is 600 micrograms/ml, which is three times higher than that for the enzyme similarly prepared from liver. The time course of the reaction for the form I enzyme is increasing over the first 40 min and becomes nearly linear thereafter. Form I is not stimulated by either calcium or cyclic nucleotides, but is inhibited by polyamines, pyrophosphate, and high concentrations of GTP. Form II enzyme is prepared by homogenization of nuclei in hypotonic buffer. It has the same ATP and poly(A) optima as the form I enzyme but displays linear kinetics over a 60-min time course. It is slightly stimulated by cGMP and cAMP and strongly inhibited by spermine, sodium pyrophosphate, and high concentrations of GTP.
与大鼠肝脏一样,当在高渗条件下制备细胞核时,大鼠脑的聚腺苷酸[poly(A)]聚合酶主要位于核液中。该酶可以两种形式从细胞核中释放出来。形式I是通过在0℃下将细胞核在低渗缓冲液中温和孵育制备的。它的最佳锰浓度为0.6 mM,最佳pH值在8至9之间。ATP浓度曲线在0.2 mM处达到平稳。最佳的聚(A)引物浓度为600微克/毫升,这比从肝脏中类似制备的酶的浓度高三倍。形式I酶反应的时间进程在最初40分钟内不断增加,此后几乎呈线性。形式I不受钙或环核苷酸的刺激,但受多胺、焦磷酸和高浓度GTP的抑制。形式II酶是通过在低渗缓冲液中匀浆细胞核制备的。它与形式I酶具有相同的ATP和聚(A)最佳条件,但在60分钟的时间进程中表现出线性动力学。它受到cGMP和cAMP的轻微刺激,并受到精胺、焦磷酸钠和高浓度GTP的强烈抑制。