Nicholls D M, Teichert-Kuliszewska K, Kuliszewski M J
J Neurol Sci. 1986 Mar;73(1):97-110. doi: 10.1016/0022-510x(86)90068-7.
The activity and amount of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in muscle of young dystrophic hamsters was reduced to approximately half the level found in control animals. No changes in brain or liver enzyme activity were found. Several other glycolytic enzyme activities and creatine kinase activity in muscle were unchanged, except for modest decreases in aldolase and pyruvate kinase. To assess the synthesis of glyceraldehyde-3-phosphate dehydrogenase, the poly(A)+ RNA was isolated from muscle polysomes of dystrophic and control animals and its activity was assessed in an mRNA-dependent translation system. The translatability of the mRNA for GAPDH found in the dystrophic muscle preparations also was half of that found in the control muscle preparations. Decreases were also found in the translatability of mRNA for tropomyosin.
幼年营养不良仓鼠肌肉中甘油醛-3-磷酸脱氢酶(GAPDH)的活性和含量降至对照动物的约一半水平。未发现脑或肝酶活性有变化。除醛缩酶和丙酮酸激酶略有下降外,肌肉中的其他几种糖酵解酶活性和肌酸激酶活性未发生改变。为评估甘油醛-3-磷酸脱氢酶的合成,从营养不良和对照动物的肌肉多核糖体中分离出多聚腺苷酸(poly(A)+)RNA,并在依赖mRNA的翻译系统中评估其活性。在营养不良肌肉制剂中发现的GAPDH mRNA的可翻译性也仅为对照肌肉制剂中的一半。原肌球蛋白mRNA的可翻译性也有所下降。