Nizhnikov Anton A, Antonets Kirill S, Inge-Vechtomov Sergey G, Derkatch Irina L
a Department of Genetics and Biotechnology ; St. Petersburg State University ; St. Petersburg , Russia.
Prion. 2014;8(3):247-60. doi: 10.4161/pri.29851. Epub 2014 Nov 1.
Nonsense suppression is a readthrough of premature termination codons. It typically occurs either due to the recognition of stop codons by tRNAs with mutant anticodons, or due to a decrease in the fidelity of translation termination. In the latter case, suppressors usually promote the readthrough of different types of nonsense codons and are thus called omnipotent nonsense suppressors. Omnipotent nonsense suppressors were identified in yeast Saccharomyces cerevisiae in 1960s, and most of subsequent studies were performed in this model organism. Initially, omnipotent suppressors were localized by genetic analysis to different protein- and RNA-encoding genes, mostly the components of translational machinery. Later, nonsense suppression was found to be caused not only by genomic mutations, but also by epigenetic elements, prions. Prions are self-perpetuating protein conformations usually manifested by infectious protein aggregates. Modulation of translational accuracy by prions reflects changes in the activity of their structural proteins involved in different aspects of protein synthesis. Overall, nonsense suppression can be seen as a "phenotypic mirror" of events affecting the accuracy of the translational machine. However, the range of proteins participating in the modulation of translation termination fidelity is not fully elucidated. Recently, the list has been expanded significantly by findings that revealed a number of weak genetic and epigenetic nonsense suppressors, the effect of which can be detected only in specific genetic backgrounds. This review summarizes the data on the nonsense suppressors decreasing the fidelity of translation termination in S. cerevisiae, and discusses the functional significance of the modulation of translational accuracy.
无义抑制是对过早终止密码子的通读。它通常是由于带有突变反密码子的tRNA识别终止密码子,或者是由于翻译终止保真度的降低而发生。在后一种情况下,抑制子通常促进不同类型无义密码子的通读,因此被称为全能无义抑制子。20世纪60年代在酿酒酵母中鉴定出全能无义抑制子,随后的大多数研究都是在这种模式生物中进行的。最初,通过遗传分析将全能抑制子定位到不同的蛋白质编码基因和RNA编码基因,主要是翻译机制的组成部分。后来发现,无义抑制不仅由基因组突变引起,还由表观遗传元件——朊病毒引起。朊病毒是自我延续的蛋白质构象,通常表现为传染性蛋白质聚集体。朊病毒对翻译准确性的调节反映了其参与蛋白质合成不同方面的结构蛋白活性的变化。总体而言,无义抑制可被视为影响翻译机器准确性的事件的“表型镜像”。然而,参与调节翻译终止保真度的蛋白质范围尚未完全阐明。最近,通过发现揭示了一些弱遗传和表观遗传无义抑制子,显著扩大了这一名单,其作用只能在特定的遗传背景中检测到。本综述总结了关于酿酒酵母中降低翻译终止保真度的无义抑制子的数据,并讨论了翻译准确性调节的功能意义。