Cole M D, Mango S E
Department of Molecular Biology, Princeton University, N.J.
Enzyme. 1990;44(1-4):167-80. doi: 10.1159/000468755.
Rapid turnover of the c-myc message mediates both the low basal level of mRNA and the rapid response to changes in transcription. The primary RNA instability determinant (RID sequence) resides in the 3' untranslated region (UTR), within an 80 base region that is rich in A and U residues. In contrast to granulocyte-macrophage colony-stimulating factor (GM-CSF) mRNA in which the RID sequence has been mapped to a repeating AUUUA sequence, mutation of the only copy of this sequence in the c-myc 3' UTR has no effect on RNA turnover. Thus the c-myc RID sequence appears to be quite different from that of GM-CSF, which may account for the differential regulation of half-life exhibited by these mRNAs. c-myc mRNA turnover is also tightly coupled to translation since translational inhibitors stabilize this mRNA. Mutation of the initiating AUG to a termination codon stabilizes c-myc RNA, arguing that loading with polysomes (perhaps accompanied by localization on the cytoskeleton) is also required for proper message turnover.
c-myc信使RNA的快速周转介导了mRNA的低基础水平以及对转录变化的快速反应。主要的RNA不稳定决定因素(RID序列)位于3'非翻译区(UTR)内一个富含A和U残基的80个碱基区域。与粒细胞-巨噬细胞集落刺激因子(GM-CSF)mRNA不同,GM-CSF的RID序列已被定位到一个重复的AUUUA序列,而c-myc 3'UTR中该序列的唯一拷贝发生突变对RNA周转没有影响。因此,c-myc的RID序列似乎与GM-CSF的RID序列有很大不同,这可能解释了这些mRNA在半衰期上的差异调节。c-myc mRNA的周转也与翻译紧密耦合,因为翻译抑制剂会使这种mRNA稳定。起始AUG突变为终止密码子会使c-myc RNA稳定,这表明多核糖体的负载(可能伴随着在细胞骨架上的定位)对于正确的信使RNA周转也是必需的。