Division of Virology, Department of Pathology, University of Cambridge, Cambridge CB2 1QP, UK.
Open Biol. 2012 Oct;2(10):120109. doi: 10.1098/rsob.120109.
Programmed ribosomal frameshifting is used in the expression of many virus genes and some cellular genes. In eukaryotic systems, the most well-characterized mechanism involves -1 tandem tRNA slippage on an X_XXY_YYZ motif. By contrast, the mechanisms involved in programmed +1 (or -2) slippage are more varied and often poorly characterized. Recently, a novel gene, PA-X, was discovered in influenza A virus and found to be expressed via a shift to the +1 reading frame. Here, we identify, by mass spectrometric analysis, both the site (UCC_UUU_CGU) and direction (+1) of the frameshifting that is involved in PA-X expression. Related sites are identified in other virus genes that have previously been proposed to be expressed via +1 frameshifting. As these viruses infect insects (chronic bee paralysis virus), plants (fijiviruses and amalgamaviruses) and vertebrates (influenza A virus), such motifs may form a new class of +1 frameshift-inducing sequences that are active in diverse eukaryotes.
程序性核糖体移码在许多病毒基因和一些细胞基因的表达中被使用。在真核系统中,最典型的机制涉及在 X_XXY_YYZ 模体上 -1 串联 tRNA 滑动。相比之下,涉及程序性 +1(或-2)滑动的机制更加多样化,并且通常特征描述较差。最近,在甲型流感病毒中发现了一种新的基因 PA-X,并发现它通过移码到+1 阅读框来表达。在这里,我们通过质谱分析鉴定了参与 PA-X 表达的移码的位点(UCC_UUU_CGU)和方向(+1)。在之前被提议通过+1 移码表达的其他病毒基因中也鉴定到了相关的位点。由于这些病毒感染昆虫(慢性蜜蜂麻痹病毒)、植物(斐济病毒和嵌合病毒)和脊椎动物(甲型流感病毒),因此这些模体可能形成了一类新的+1 移码诱导序列,它们在不同的真核生物中都具有活性。