Williams K P, Martindale K A, Bartel D P
Department of Biology, Indiana University, 1001 East 3rd Street, Bloomington, IN 47405-3700, USA.
EMBO J. 1999 Oct 1;18(19):5423-33. doi: 10.1093/emboj/18.19.5423.
The bacterial ribosome switches from an mRNA lacking an in-frame stop codon and resumes translation on a specialized RNA known as tmRNA, SsrA or 10Sa RNA. We find that the ribosome can reach and use the extreme 3' terminal codon of the defective mRNA prior to switching. The first triplet to be translated in tmRNA (the resume codon) is determined at two levels: distant elements in tmRNA restrict resume codon choice to a narrow window and local upstream elements provide precision. Insights from a randomization-selection experiment secure the alignment of tmRNA sequences from diverse species. The triplet UA(A/G) (normally recognized as a stop codon by release factor-1) is strongly conserved two nucleotides upstream of the resume codon. The central adenosine of this triplet is essential for tmRNA activity. The reading frame of tmRNA is determined differently from all other known reading frames in that the first translated codon is not specified by a particular tRNA anticodon.
细菌核糖体从缺乏读框内终止密码子的信使核糖核酸(mRNA)上转换下来,并在一种名为转运信使核糖核酸(tmRNA)、SsrA或10Sa RNA的特殊核糖核酸上重新开始翻译。我们发现,核糖体在转换之前能够到达并利用缺陷mRNA的极端3'末端密码子。tmRNA中第一个要翻译的三联体(重新开始密码子)在两个层面上被确定:tmRNA中的远距离元件将重新开始密码子的选择限制在一个狭窄的窗口内,而局部上游元件则提供精确性。随机化选择实验的见解确保了来自不同物种的tmRNA序列的比对。三联体UA(A/G)(通常被释放因子-1识别为终止密码子)在重新开始密码子上游两个核苷酸处高度保守。这个三联体的中央腺苷对于tmRNA的活性至关重要。tmRNA的阅读框与所有其他已知阅读框的确定方式不同,因为第一个被翻译的密码子不是由特定的转运核糖核酸(tRNA)反密码子指定的。