Börner G V, Mörl M, Wissinger B, Brennicke A, Schmelzer C
Institut für Genetik und Mikrobiologie, Universität München, Germany.
Mol Gen Genet. 1995 Mar 20;246(6):739-44. doi: 10.1007/BF00290721.
The trans-splicing group II intron c/d in the Oenothera mitochondrial nad1 gene is modified by RNA editing in domain 6. This C-to-U conversion generates the typical domain 6 structure, which prompted us to speculate that this RNA editing event might be essential for splicing. To test this hypothesis, we investigated the influence of unedited and edited sequences of the Oenothera intron on splicing in vitro. The stem of domain 6 of intron nad1-c/d was transplanted into the autocatalytic yeast intron aI5c, yielding chimeras with the genomic C and the edited U, respectively, 5' of the branchpoint A. When incubated under self-splicing conditions, only the edited chimera was released as a lariat, while the precursor with the genomically coded C remained inactive. Our results support the hypothesis that Oenothera group II intron nad1-c/d cannot be spliced from the primary transcript without previous editing in domain 6.
月见草线粒体nad1基因中的反式剪接II组内含子c/d在结构域6中通过RNA编辑进行修饰。这种C到U的转换产生了典型的结构域6结构,这促使我们推测这种RNA编辑事件可能对剪接至关重要。为了验证这一假设,我们研究了月见草内含子未编辑和编辑序列对体外剪接的影响。内含子nad1-c/d结构域6的茎被移植到自催化酵母内含子aI5c中,分别产生在分支点A的5'端带有基因组C和编辑后的U的嵌合体。在自我剪接条件下孵育时,只有编辑后的嵌合体以套索状形式释放,而具有基因组编码C的前体仍然无活性。我们的结果支持这样的假设,即月见草II组内含子nad1-c/d在结构域6中没有预先编辑的情况下不能从初级转录本中剪接出来。