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Extensive mis-splicing of a bi-partite plant mitochondrial group II intron

机译:双重植物线粒体第二类内含子的广泛错接

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摘要

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.
机译:种子植物线粒体nad5基因的表达涉及两个反式分裂事件,这些事件去除了片段化的II组内含子,并将小的中央外显子c连接到外显子b和d。我们表明,在单子叶植物和双子叶植物中,两性内含子2发生广泛的错接,导致异常剪接产物的形成,其中外显子c连接到外显子b的各个位点。这些错误剪接的产物积聚到与正确剪接的mRNA相当或更高的水平。我们建议错配可能是由于外显子a和外显子c下游的部分两性内含子3之间的碱基配对对内含子2施加的折叠限制而引起的。与此假设相符,我们发现月见草线粒体中不会发生错剪接,内含子3进一步被片段化,使得预测的碱基配对区域不与外显子c共价连接。我们的发现表明内含子片段化可能导致错剪,可通过进一步内含子片段化来纠正。

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