Hordeĭchyk O I, Shcherbatenko I S
Mikrobiol Z. 2010 Nov-Dec;72(6):58-65.
A computer search of the suppressive terminal codons of translation (STCT) of plant virus genes in genetic banks and a comparative analysis of their suppression contexts were performed. Using "readthrough" and "transl_except" as key words STCT were found in replicase and coat protein genes in 118 strains of ssRNA plant viruses, belonging to 68 species from 13 genera. It was established that in genomes of plant viruses the most frequent suppressive termination codon is UAG (167 from 211, 79.1%), less frequent--UGA (37 from 211, 17.5%) and rare--UAA (7 from 211, 3.3%). The most of weak suppressive terminal codons contain in +4 position caauua, cgguuu, gggugc, ggaggc or guagac, the hexanucleotide sites that are believed to be important (consensus) elements of leaky stop codons in positive-sense ssRNA viruses of plants, animals and microorganisms. At the same time one can observe great variability of consensus nucleotide sites in many viral genes as well as additional positions of hexanucleotide sites in different reading frames and at different distances from terminal codons. Availability of clasters of identical nucleotide sites, in different virus genera, located as far as some hundred bases from terminal codons is a characteristic feature of suppressive terminal codons. Results obtained support a hypothesis that the translation termination efficiency as well as stop codon readthrough may be determinated at genome or gene level rather than by a short nucleotide context surrounding stop codons.
对基因库中植物病毒基因的翻译抑制性终止密码子(STCT)进行了计算机搜索,并对其抑制背景进行了比较分析。以“通读”和“翻译排除”为关键词,在118株单链RNA植物病毒的复制酶和外壳蛋白基因中发现了STCT,这些病毒属于13个属的68个物种。研究发现,在植物病毒基因组中,最常见的抑制性终止密码子是UAG(211个中有167个,占79.1%),较不常见的是UGA(211个中有37个,占17.5%),罕见的是UAA(211个中有7个,占3.3%)。大多数弱抑制性终止密码子在+4位置包含caauua、cgguuu、gggugc、ggaggc或guagac,这些六核苷酸位点被认为是植物、动物和微生物正义单链RNA病毒中泄漏终止密码子的重要(共有)元件。同时,可以观察到许多病毒基因中共识核苷酸位点的巨大变异性,以及不同阅读框中六核苷酸位点在距终止密码子不同距离处的额外位置。在不同病毒属中,距终止密码子数百个碱基处存在相同核苷酸位点的簇,这是抑制性终止密码子的一个特征。所得结果支持了一个假设,即翻译终止效率以及终止密码子的通读可能在基因组或基因水平上决定,而不是由终止密码子周围的短核苷酸背景决定。