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Horizontal Transfer and Gene Conversion as an Important Driving Force in Shaping the Landscape of Mitochondrial Introns

机译:水平转移和基因转化是塑造线粒体内含子景观的重要驱动力

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摘要

Group I introns are highly dynamic and mobile, featuring extensive presence-absence variation and widespread horizontal transfer. Group I introns can invade intron-lacking alleles via intron homing powered by their own encoded homing endonuclease gene (HEG) after horizontal transfer or via reverse splicing through an RNA intermediate. After successful invasion, the intron and HEG are subject to degeneration and sequential loss. It remains unclear whether these mechanisms can fully address the high dynamics and mobility of group I introns. Here, we found that HEGs undergo a fast gain-and-loss turnover comparable with introns in the yeast mitochondrial 21S-rRNA gene, which is unexpected, as the intron and HEG are generally believed to move together as a unit. We further observed extensively mosaic sequences in both the introns and HEGs, and evidence of gene conversion between HEG-containing and HEG-lacking introns. Our findings suggest horizontal transfer and gene conversion can accelerate HEG/intron degeneration and loss, or rescue and propagate HEG/introns, and ultimately result in high HEG/intron turnover rate. Given that up to 25% of the yeast mitochondrial genome is composed of introns and most mitochondrial introns are group I introns, horizontal transfer and gene conversion could have served as an important mechanism in introducing mitochondrial intron diversity, promoting intron mobility and consequently shaping mitochondrial genome architecture.
机译:第一组内含子具有高度的动态性和移动性,具有广泛的在场-不在场变化和广泛的水平转移。在水平转移后,I组内含子可以通过由自己编码的归巢内切核酸酶基因(HEG)提供动力的内含子归巢,或通过RNA中间体的反向剪接,进入缺少内含子的等位基因。成功入侵后,内含子和HEG易变性和顺序丢失。尚不清楚这些机制是否可以完全解决I组内含子的高动态和迁移性。在这里,我们发现HEG与酵母线粒体21S-rRNA基因中的内含子相比具有快速的损益转换,这是出乎意料的,因为通常认为内含子和HEG可以作为一个单元一起移动。我们进一步观察到内含子和HEG中都存在广泛的镶嵌序列,并且在含HEG和不含HEG的内含子之间进行了基因转换的证据。我们的研究结果表明水平转移和基因转化可以加速HEG /内含子的变性和损失,或抢救和繁殖HEG /内含子,最终导致高HEG /内含子更新率。鉴于多达25%的酵母线粒体基因组由内含子组成,而大多数线粒体内含子是第I组内含子,因此水平转移和基因转化可能是引入线粒体内含子多样性,促进内含子迁移并从而塑造线粒体基因组的重要机制建筑。

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