Dobson D E, Groves D L, Spiegelman B M
J Biol Chem. 1987 Feb 5;262(4):1804-9.
We have studied the structure and regulation of glycerophosphate dehydrogenase (GPD) mRNA during mouse adipocyte and muscle cell differentiation. This message has a size of 2.8 kilobases that includes a coding segment of 1050 bases and a large untranslated 3' end of about 1700 bases. There is a high degree of amino acid homology (91%) between the mouse adipocyte and rabbit muscle GPD proteins. GPD mRNA is not detected in myoblasts, but, as in adipogenesis, it is expressed upon differentiation into myotubes. The modulation of GPD mRNA by cyclic AMP analogues and tumor necrosis factor has been examined in both adipocytes and myotubes. Dibutyryl cAMP or 8-bromo-cAMP causes a large reduction of GPD mRNA levels in both cell types, with less than 20% remaining after 18 h of treatment. Tumor necrosis factor effects a dramatic and rapid reduction in GPD mRNA in fat cells and a slower but significant decrease in the level of this mRNA in muscle cells. These results indicate that GPD gene expression is linked to cell differentiation in both fat and muscle cells, and suggest certain similarities in hormonal modulation in both cell types.
我们研究了小鼠脂肪细胞和肌肉细胞分化过程中甘油磷酸脱氢酶(GPD)mRNA的结构与调控。该信使RNA大小为2.8千碱基,包括一个1050个碱基的编码区段和一个约1700个碱基的大型非翻译3'末端。小鼠脂肪细胞GPD蛋白与兔肌肉GPD蛋白之间存在高度的氨基酸同源性(91%)。在成肌细胞中未检测到GPD mRNA,但与脂肪生成过程一样,在分化为肌管时它会表达。已在脂肪细胞和肌管中研究了环磷酸腺苷类似物和肿瘤坏死因子对GPD mRNA的调节作用。二丁酰环磷腺苷或8-溴环磷腺苷会使两种细胞类型中的GPD mRNA水平大幅降低,处理18小时后剩余不到20%。肿瘤坏死因子会使脂肪细胞中的GPD mRNA急剧且迅速降低,使肌肉细胞中该mRNA水平缓慢但显著下降。这些结果表明,GPD基因表达与脂肪细胞和肌肉细胞的分化相关,并提示两种细胞类型在激素调节方面存在某些相似之处。