Department of Biology, McGill University, Montreal, Quebec H3A 1B1, Canada.
Nucleic Acids Res. 2010 Jan;38(3):996-1008. doi: 10.1093/nar/gkp994. Epub 2009 Nov 17.
Expression of the seed plant mitochondrial nad5 gene involves two trans-splicing events that remove fragmented group II introns and join the small, central exon c to exons b and d. We show that in both monocot and eudicot plants, extensive mis-splicing of the bi-partite intron 2 takes place, resulting in the formation of aberrantly spliced products in which exon c is joined to various sites within exon b. These mis-spliced products accumulate to levels comparable to or greater than that of the correctly spliced mRNA. We suggest that mis-splicing may result from folding constraints imposed on intron 2 by base-pairing between exon a and a portion of the bi-partite intron 3 downstream of exon c. Consistent with this hypothesis, we find that mis-splicing does not occur in Oenothera mitochondria, where intron 3 is further fragmented such that the predicted base-pairing region is not covalently linked to exon c. Our findings suggest that intron fragmentation may lead to mis-splicing, which may be corrected by further intron fragmentation.
植物线粒体 nad5 基因的表达涉及两个转剪接事件,该过程去除了碎片化的组 II 内含子,并将小的、中央的外显子 c 与外显子 b 和 d 连接起来。我们表明,在单子叶植物和双子叶植物中,二部分的内含子 2 存在广泛的错误剪接,导致形成异常剪接产物,其中外显子 c 与外显子 b 内的各种位点连接。这些错误剪接的产物积累到与正确剪接的 mRNA 相当或更高的水平。我们认为,错误剪接可能是由于外显子 a 与外显子 c 下游的二部分内含子 3 的一部分之间的碱基配对对内含子 2 施加的折叠限制所致。与该假设一致,我们发现,在油桐线粒体中不会发生错误剪接,在油桐线粒体中,内含子 3 进一步碎片化,使得预测的碱基配对区域与外显子 c 没有共价连接。我们的发现表明,内含子碎片化可能导致错误剪接,而进一步的内含子碎片化可能会纠正错误剪接。