Binder S, Marchfelder A, Brennicke A, Wissinger B
Institut für Genbiologische Forschung, Berlin, Federal Republic of Germany.
J Biol Chem. 1992 Apr 15;267(11):7615-23.
The complete open reading frame of subunit 2 of the NADH dehydrogenase in Oenothera mitochondria is split into five exons. The first two and the last three exons are encoded in distant genomic locations and are transcribed separately. Three tRNA genes coding for tRNA(Cys), tRNA(Asn), and tRNA(Tyr) are located upstream of the terminal three exons c, d, and e. The genomic distance, the interspersed tRNA genes, and the group II intron sequences flanking the two separated exons suggest trans-splicing to be required to connect exons b and c. Maturation of the mRNA includes RNA editing at 36 sites in the open reading frame. Three RNA editing events are observed in the split group II intron sequences. Two of these events allow after editing additional base pairings in the secondary structure, one in the stem of domain I, the other in the putative trans-pairing region of domain IV. These RNA editings may thus be involved in the trans-splicing reaction.
月见草属线粒体中烟酰胺腺嘌呤二核苷酸脱氢酶亚基2的完整开放阅读框被分成五个外显子。前两个外显子和最后三个外显子编码于相距较远的基因组位置,且分别转录。编码tRNA(Cys)、tRNA(Asn)和tRNA(Tyr)的三个tRNA基因位于末端三个外显子c、d和e的上游。基因组距离、散布的tRNA基因以及两个分离外显子侧翼的II类内含子序列表明需要反式剪接来连接外显子b和c。mRNA的成熟包括开放阅读框中36个位点的RNA编辑。在分裂的II类内含子序列中观察到三个RNA编辑事件。其中两个事件在编辑后允许二级结构中有额外的碱基配对,一个在结构域I的茎中,另一个在结构域IV的假定反式配对区域中。因此,这些RNA编辑可能参与反式剪接反应。