Sato A, Noda K, Natori Y
Biochim Biophys Acta. 1979 Feb 27;561(2):475-83. doi: 10.1016/0005-2787(79)90155-2.
In order to understand the mechanism of decreased protein synthesis in the liver of rats fed a protein-free diet, the average polypeptide chain assembly time (tc) was measured by the method of Mathews et al. (J. Biol. Chem. (1973) 248, 1329). For rats fed a normal diet, tc in liver in vivo was 1.28 min. A 10-day period of protein depletion led to a value of tc = 2.08 min, corresponding to a 38% depression in polypeptide elongation rate. Protein depletion caused an extensive breakdown of hepatic polysomes and refeeding of a complete mixture of amino acids resulted in rapid recovery of polysomal profile. But tc in the liver of the refed animals gave still depressed value of 1.95 min. The amount and size distribution of poly(A)-containing mRNA in the liver, as determined by [3H]poly(U) hybridization, were the same for normal and depleted groups. These results suggest that both initiation and elongation steps of protein synthesis are depressed in the liver of protein-depleted rats. Refeeding of amino acid mixture rapidly restores initiation but not elongation activity.
为了了解无蛋白饮食喂养的大鼠肝脏中蛋白质合成减少的机制,采用Mathews等人(《生物化学杂志》(1973年)248卷,1329页)的方法测量了平均多肽链组装时间(tc)。对于正常饮食喂养的大鼠,肝脏中体内的tc为1.28分钟。10天的蛋白质缺乏期导致tc值为2.08分钟,这相当于多肽延伸率降低了38%。蛋白质缺乏导致肝脏多核糖体大量分解,重新喂食完整的氨基酸混合物可使多核糖体图谱迅速恢复。但重新喂食动物的肝脏中的tc仍为1.95分钟,仍处于较低水平。通过[3H]聚尿苷酸杂交测定,正常组和缺乏组肝脏中含聚腺苷酸的mRNA的量和大小分布相同。这些结果表明,蛋白质缺乏大鼠肝脏中蛋白质合成的起始和延伸步骤均受到抑制。重新喂食氨基酸混合物可迅速恢复起始活性,但不能恢复延伸活性。