Laforest Marie-Josée, Bullerwell Charles E, Forget Lise, Lang B Franz
Département de Biochimie, Université de Montréal, 2900, Boulevard Edouard Montpetit, C.P. 6128, Succursale Centre-Ville, Québec H3C 3J7, Canada.
RNA. 2004 Aug;10(8):1191-9. doi: 10.1261/rna.7330504. Epub 2004 Jul 9.
5' tRNA editing has been demonstrated to occur in the mitochondria of the distantly related rhizopod amoeba Acanthamoeba castellanii and the chytridiomycete fungus Spizellomyces punctatus. In these organisms, canonical tRNA structures are restored by removing mismatched nucleotides at the first three 5' positions and replacing them with nucleotides capable of forming Watson-Crick base pairs with their 3' counterparts. This form of editing seems likely to occur in members of Amoebozoa other than A. castellanii, as well as in members of Heterolobosea. Evidence for 5' tRNA editing has not been found to date, however, in any other fungus including the deeply branching chytridiomycete Allomyces macrogynus. We predicted that a similar form of tRNA editing would occur in members of the chytridiomycete order Monoblepharidales based on the analysis of complete mitochondrial tRNA complements. This prediction was confirmed by analysis of tRNA sequences using a tRNA circularization/RT-PCR-based approach. The presence of partially and completely unedited tRNAs in members of the Monoblepharidales suggests the involvement of a 5'-to-3' exonuclease rather than an endonuclease in removing the three 5' nucleotides from a tRNA substrate. Surprisingly, analysis of the mtDNA of the chytridiomycete Rhizophydium brooksianum, which branches as a sister group to S. punctatus in molecular phylogenies, did not suggest the presence of editing. This prediction was also confirmed experimentally. The absence of tRNA editing in R. brooksianum raises the possibility that 5' tRNA editing may have evolved twice independently within Chytridiomycota, once in the lineage leading to S. punctatus and once in the lineage leading to the Monoblepharidales.
5'端tRNA编辑已在亲缘关系较远的根足类变形虫卡氏棘阿米巴和壶菌纲真菌点状油壶菌的线粒体中得到证实。在这些生物中,通过去除前三个5'位置的错配核苷酸并用能够与其3'对应物形成沃森-克里克碱基对的核苷酸进行替换,恢复了标准的tRNA结构。这种编辑形式似乎可能发生在除卡氏棘阿米巴之外的变形虫门成员以及异叶足虫纲成员中。然而,迄今为止,在包括深分支壶菌大果全毛菌在内的任何其他真菌中均未发现5'端tRNA编辑的证据。基于对完整线粒体tRNA互补序列的分析,我们预测壶菌目单毛菌科的成员中会发生类似形式的tRNA编辑。使用基于tRNA环化/逆转录-聚合酶链反应的方法对tRNA序列进行分析,证实了这一预测。单毛菌科成员中存在部分和完全未编辑的tRNA,这表明在从tRNA底物中去除三个5'核苷酸的过程中涉及5'至3'核酸外切酶而非核酸内切酶。令人惊讶的是,对布鲁克斯根壶菌线粒体DNA的分析(在分子系统发育中,布鲁克斯根壶菌作为点状油壶菌的姐妹群分支)并未表明存在编辑现象。这一预测也通过实验得到了证实。布鲁克斯根壶菌中不存在tRNA编辑,这增加了5'端tRNA编辑可能在壶菌门内独立进化两次的可能性,一次在导致点状油壶菌的谱系中,另一次在导致单毛菌科的谱系中。