Soma Akiko
Graduate School of Horticulture, Chiba University Matsudo, Japan.
Front Genet. 2014 Apr 1;5:63. doi: 10.3389/fgene.2014.00063. eCollection 2014.
A number of genome analyses and searches using programs that focus on the RNA-specific bulge-helix-bulge (BHB) motif have uncovered a wide variety of disrupted tRNA genes. The results of these analyses have shown that genetic information encoding functional RNAs is described in the genome cryptically and is retrieved using various strategies. One such strategy is represented by circularly permuted tRNA genes, in which the sequences encoding the 5'-half and 3'-half of the specific tRNA are separated and inverted on the genome. Biochemical analyses have defined a processing pathway in which the termini of tRNA precursors (pre-tRNAs) are ligated to form a characteristic circular RNA intermediate, which is then cleaved at the acceptor-stem to generate the typical cloverleaf structure with functional termini. The sequences adjacent to the processing site located between the 3'-half and the 5'-half of pre-tRNAs potentially form a BHB motif, which is the dominant recognition site for the tRNA-intron splicing endonuclease, suggesting that circularization of pre-tRNAs depends on the splicing machinery. Some permuted tRNAs contain a BHB-mediated intron in their 5'- or 3'-half, meaning that removal of an intron, as well as swapping of the 5'- and 3'-halves, are required during maturation of their pre-tRNAs. To date, 34 permuted tRNA genes have been identified from six species of unicellular algae and one archaeon. Although their physiological significance and mechanism of development remain unclear, the splicing system of BHB motifs seems to have played a key role in the formation of permuted tRNA genes. In this review, current knowledge of circularly permuted tRNA genes is presented and some unanswered questions regarding these species are discussed.
一些基因组分析以及使用聚焦于RNA特异性凸起-螺旋-凸起(BHB)基序的程序进行的搜索,发现了各种各样被破坏的tRNA基因。这些分析结果表明,编码功能性RNA的遗传信息在基因组中是隐秘描述的,并通过各种策略来检索。其中一种策略由环形排列的tRNA基因代表,在这种基因中,编码特定tRNA 5'半段和3'半段的序列在基因组上是分开且倒置的。生化分析确定了一条加工途径,其中tRNA前体(pre-tRNA)的末端被连接形成一种特征性的环状RNA中间体,然后该中间体在接受茎处被切割以产生具有功能性末端的典型三叶草结构。与位于pre-tRNA的3'半段和5'半段之间的加工位点相邻的序列可能形成一个BHB基序,这是tRNA内含子剪接内切核酸酶的主要识别位点,表明pre-tRNA的环化依赖于剪接机制。一些重排的tRNA在其5'或3'半段中含有一个由BHB介导的内含子,这意味着在其pre-tRNA成熟过程中,除了5'和3'半段的交换外,还需要去除一个内含子。迄今为止,已从六种单细胞藻类和一种古生菌中鉴定出34个重排的tRNA基因。尽管它们的生理意义和发育机制仍不清楚,但BHB基序的剪接系统似乎在重排tRNA基因的形成中起了关键作用。在这篇综述中,介绍了关于环形排列的tRNA基因的当前知识,并讨论了有关这些物种的一些未解决的问题。