Filippova G N, Spitkovskiĭ D D, Boĭkov P Ia, Alesenko A V
Mol Biol (Mosk). 1989 May-Jun;23(3):843-50.
Injection of sublethal doses of cycloheximide (CHI) to rats allowed to reveal three stages in the dynamics of protein synthesis: 1) suppression stage (0-6 hrs), 2) regeneration stage (6-12 hrs), 3) stimulation stage (6-12 hrs). RNA-polymerases are activated when protein synthesis is inhibited. The stimulation stage precedes the activation of DNA replication. This model of DNA replication induced by CHI is specified by the expression of various cell oncogenes (c-fos, c-mys, p53, c-Ha-ras, c-sis, c-src). The investigated oncogenes may be divided into 4 groups according to the character of their expression. 1. Oncogenes (c-fos, c-myc) are switched on step-by-step 1 hour after CHI injection, the superexpression of the oncogenes being comparatively short. Maximum expression of c-fos and c-myc oncogenes is registered after 2-3 hours, respectively. 2./p53 oncogene expression increases within a few hours' after CHI injection and manifests itself at all three stages of protein synthesis till DNA replication. 3. c-Ha-ras oncogene is expressed at a high level in control and experimental animals. 4. Expression of c-sis and c-src oncogenes are absent both before and after CHI injection. Sublethal doses of CHI have the same effect on oncogene expression as the lethal ones.
给大鼠注射亚致死剂量的放线菌酮(CHI),可揭示蛋白质合成动态变化的三个阶段:1)抑制阶段(0 - 6小时),2)再生阶段(6 - 12小时),3)刺激阶段(6 - 12小时)。当蛋白质合成受到抑制时,RNA聚合酶被激活。刺激阶段先于DNA复制的激活。由CHI诱导的这种DNA复制模型由各种细胞癌基因(c - fos、c - mys、p53、c - Ha - ras、c - sis、c - src)的表达所决定。根据其表达特征,所研究的癌基因可分为4组。1. 癌基因(c - fos、c - myc)在注射CHI后1小时逐步开启,癌基因的超表达相对较短。c - fos和c - myc癌基因的最大表达分别在2 - 3小时后出现。2. p53癌基因表达在注射CHI后数小时内增加,并在蛋白质合成直至DNA复制的所有三个阶段都有表现。3. c - Ha - ras癌基因在对照动物和实验动物中均高水平表达。4. c - sis和c - src癌基因在注射CHI前后均无表达。亚致死剂量的CHI对癌基因表达的影响与致死剂量相同。