Hu Y W, Brosnan M E
Arch Biochem Biophys. 1987 May 1;254(2):637-41. doi: 10.1016/0003-9861(87)90147-0.
Ornithine decarboxylase-antizyme was induced in mammary gland of fasted lactating rats by administration of 1,3-diaminopropan-2-ol. Antizyme from mammary gland showed similar chemical and kinetic behavior to that previously reported by Canellakis and co-workers for antizyme from liver [J. S. Heller, W. F. Fong, and E. S. Canellakis (1976) Proc. Natl. Acad. Sci. USA 72, 1858-1862]; specifically the inhibitor was nondialyzable, heat labile, and ribonuclease insensitive, and the inhibition was time independent, proportional to the concentration of antizyme present, and noncompetitive with respect to the substrate, ornithine. However, ornithine decarboxylase-antizyme from mammary gland eluted from Sephadex G-75 with an apparent molecular mass of 55 kDa, compared with 27 kDa, for antizyme from liver under identical conditions. The elution pattern was unaffected by the presence of high salt concentrations, indicating that the larger size was not due to macromolecular complexes. The presence of antizyme-ornithine decarboxylase complex was detected in mammary gland of untreated lactating rats fasted for 6 or 24 h, thus indicating that antizyme plays a role in the regulation of ornithine decarboxylase in mammary gland under physiological conditions.
通过给予1,3 - 二氨基丙 - 2 - 醇,在禁食的泌乳大鼠乳腺中诱导出鸟氨酸脱羧酶抗酶。来自乳腺的抗酶表现出与Canellakis及其同事先前报道的来自肝脏的抗酶相似的化学和动力学行为[J. S. Heller, W. F. Fong, and E. S. Canellakis (1976) Proc. Natl. Acad. Sci. USA 72, 1858 - 1862];具体而言,该抑制剂不可透析、对热不稳定且对核糖核酸酶不敏感,并且抑制作用与时间无关,与存在的抗酶浓度成正比,且对底物鸟氨酸无竞争性。然而,在相同条件下,从Sephadex G - 75洗脱的来自乳腺的鸟氨酸脱羧酶抗酶的表观分子量为55 kDa,而来自肝脏的抗酶为27 kDa。洗脱模式不受高盐浓度存在的影响,表明较大的尺寸不是由于大分子复合物。在禁食6小时或24小时的未处理泌乳大鼠的乳腺中检测到抗酶 - 鸟氨酸脱羧酶复合物,因此表明抗酶在生理条件下的乳腺鸟氨酸脱羧酶调节中起作用。