Del Monte U, Capaccioli S, Neri Cini G, Perego R, Caldini R, Chevanne M
Biochem J. 1986 May 15;236(1):163-9. doi: 10.1042/bj2360163.
The tRNA content and aminoacyl-tRNA synthetases of regenerating liver in the phase of rapid growth were compared with those of livers from both intact and sham-operated rats. At 48 h after hepatectomy, the amount of active tRNA (called 'total acceptor capacity') is significantly higher in regenerating liver than in control livers, owing to a general, possibly not uniform, increase in the various tRNA families, which suggests that it may contribute to the increased protein synthesis and to decreased protein degradation as well. The activities of most, but not of all, aminoacyl-tRNA synthetases in cell sap of regenerating liver tend to be greater than normal. Increased activity of histidyl-tRNA synthetase fits in with the possibility that the mechanisms that control the rate of protein degradation through aminoacylation of tRNAHis in cultured cells [Scornik (1983) J. Biol. Chem. 258, 882-886] also operate in the liver and play a role in regeneration. Sedimentation analysis of cell sap in sucrose density gradients shows a shift of prolyl-tRNA synthetase activity toward the high-Mr form in regenerating liver. This change might be related to the positive protein balance and to growth in vivo, since it is also observed in the anaplastic Yoshida ascites hepatoma AH 130.
将快速生长阶段再生肝脏的tRNA含量和氨酰-tRNA合成酶与完整大鼠和假手术大鼠肝脏的tRNA含量和氨酰-tRNA合成酶进行了比较。肝切除术后48小时,再生肝脏中活性tRNA的量(称为“总受体容量”)显著高于对照肝脏,这是由于各种tRNA家族普遍增加(可能并不均匀),这表明它可能有助于增加蛋白质合成以及减少蛋白质降解。再生肝脏细胞液中大多数(但不是全部)氨酰-tRNA合成酶的活性往往高于正常水平。组氨酰-tRNA合成酶活性的增加符合以下可能性,即通过培养细胞中tRNAHis的氨酰化来控制蛋白质降解速率的机制[斯科尔尼克(1983年)《生物化学杂志》258卷,882 - 886页]在肝脏中也起作用并在再生中发挥作用。在蔗糖密度梯度中对细胞液进行沉降分析表明,再生肝脏中脯氨酰-tRNA合成酶活性向高分子量形式转移。这种变化可能与体内的正蛋白质平衡和生长有关,因为在间变性吉田腹水肝癌AH 130中也观察到了这种变化。