Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2012 Sep 11;109(37):14852-7. doi: 10.1073/pnas.1206582109. Epub 2012 Aug 27.
Ribosomal frameshifting entails slippage of the translational machinery during elongation. Frameshifting permits expression of more than one polypeptide from an otherwise monocistronic mRNA, and can restore expression of polypeptides in the face of frameshift mutations. A common mutation conferring acyclovir resistance in patients with herpes simplex virus disease deletes one cytosine from a run of six cytosines (C-chord) in the viral thymidine kinase (tk) gene. However, this mutation does not abolish TK activity, which is important for pathogenicity. To investigate how this mutant retains TK activity, we engineered and analyzed viruses expressing epitope-tagged TK. We found that the mutant's TK activity can be accounted for by low levels of full-length TK polypeptide produced by net -1 frameshifting during translation. The efficiency of frameshifting was relatively high, 3-5%, as the polypeptide from the reading frame generated by the deletion, which lacks stop codons (nonstop), was poorly expressed mainly because of inefficient protein synthesis. Stop codons introduced into this reading frame greatly increased its expression, but greatly decreased the level of full-length TK, indicating that frameshifting is strongly stimulated by a new mechanism, nonstop mRNA, which we hypothesize involves stalling of ribosomes on the polyA tail. Mutational studies indicated that frameshifting occurs on or near the C-chord, a region lacking a canonical slippery sequence. Nonstop stimulation of frameshifting also occurred when the C-chord was replaced with a canonical slippery sequence from HIV. This mechanism thus permits biologically and clinically relevant TK synthesis, and may occur more generally.
核糖体移码涉及到在延伸过程中翻译机制的滑动。移码允许从单顺反子 mRNA 表达多个多肽,并且可以在面对移码突变时恢复多肽的表达。在单纯疱疹病毒疾病患者中赋予阿昔洛韦耐药性的常见突变从病毒胸苷激酶 (tk) 基因中的六个胞嘧啶的连续序列 (C 弦) 中删除一个胞嘧啶。然而,这种突变并没有消除 TK 活性,这对于致病性很重要。为了研究这种突变体如何保留 TK 活性,我们设计并分析了表达表位标记的 TK 的病毒。我们发现,突变体的 TK 活性可以通过翻译过程中净 -1 移码产生的低水平全长 TK 多肽来解释。移码的效率相对较高,为 3-5%,因为缺失的阅读框产生的多肽(无终止)缺乏终止密码子(无终止),主要由于蛋白质合成效率低下而表达不佳。在此阅读框中引入终止密码子大大增加了其表达,但大大降低了全长 TK 的水平,表明移码受到一种新机制的强烈刺激,即无终止 mRNA,我们假设它涉及核糖体在 polyA 尾巴上的停滞。突变研究表明,移码发生在 C 弦上或附近,这是一个缺乏典型滑序的区域。当 C 弦被 HIV 的典型滑序取代时,无终止对移码的刺激也会发生。因此,这种机制允许生物和临床相关的 TK 合成,并且可能更普遍地发生。