Schulz-Harder B, Graf von Keyserlingk D
Department of Anatomy I, Rheinisch-Westfälische Technische Hochschule Aachen, Federal Republic of Germany.
Histochemistry. 1988;88(3-6):587-94. doi: 10.1007/BF00570329.
The brain ribonucleases of rabbit, guinea pig, rat, mouse and gerbil were investigated by histochemical and biochemical methods. For the localization, the ribonucleases were electrophoretically transferred from cryostat sections to polyacrylamide gels. Elevated ribonuclease activities were found in the cortex, the basal ganglia, the hippocampal formation and the ventricles, whereas the corpus callosum and the internal capsule exhibited lower activities. The total RNA degrading activities of the brain extracts of the different species varied in a wide range. However, a pre-requisite for the measurement of acid soluble degradation products in the test system was the inactivation of endogeneous ribonuclease inhibitors, present in all extracts. Molecular weight analysis by means of SDS-polyacrylamide gel electrophoresis revealed a characteristic set of ribonucleases for each species, consisting of enzymes with different pH-optima.
采用组织化学和生物化学方法对兔、豚鼠、大鼠、小鼠和沙鼠的脑核糖核酸酶进行了研究。为进行定位,将核糖核酸酶从低温切片电泳转移至聚丙烯酰胺凝胶上。结果发现,皮质、基底神经节、海马结构和脑室中的核糖核酸酶活性升高,而胼胝体和内囊的活性较低。不同物种脑提取物的总RNA降解活性差异很大。然而,在测试系统中测量酸溶性降解产物的一个先决条件是使所有提取物中存在的内源性核糖核酸酶抑制剂失活。通过SDS-聚丙烯酰胺凝胶电泳进行的分子量分析揭示了每个物种一组独特的核糖核酸酶,它们由具有不同最适pH值的酶组成。