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Analysis of CACTA transposases reveals intron loss as major factor influencing their exon/intron structure in monocotyledonous and eudicotyledonous hosts

机译:CACTA转座酶的分析表明内含子丢失是影响单子叶和双子叶宿主中外显子/内含子结构的主要因素

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Background CACTA elements are DNA transposons and are found in numerous organisms. Despite their low activity, several thousand copies can be identified in many genomes. CACTA elements transpose using a ‘cut-and-paste’ mechanism, which is facilitated by a DDE transposase. DDE transposases from CACTA elements contain, despite their conserved function, different exon numbers among various CACTA families. While earlier studies analyzed the ancestral history of the DDE transposases, no studies have examined exon loss and gain with a view of mechanisms that could drive the changes. Results We analyzed 64 transposases from different CACTA families among monocotyledonous and eudicotyledonous host species. The annotation of the exon/intron boundaries showed a range from one to six exons. A robust multiple sequence alignment of the 64 transposases based on their protein sequences was created and used for phylogenetic analysis, which revealed eight different clades. We observed that the exon numbers in CACTA transposases are not specific for a host genome. We found that ancient CACTA lineages diverged before the divergence of monocotyledons and eudicotyledons. Most exon/intron boundaries were found in three distinct regions among all the transposases, grouping 63 conserved intron/exon boundaries. Conclusions We propose a model for the ancestral CACTA transposase gene, which consists of four exons, that predates the divergence of the monocotyledons and eudicotyledons. Based on this model, we propose pathways of intron loss or gain to explain the observed variation in exon numbers. While intron loss appears to have prevailed, a putative case of intron gain was nevertheless observed.
机译:背景技术CACTA元素是DNA转座子,存在于许多生物中。尽管它们的活性很低,但可以在许多基因组中鉴定出数千个拷贝。 CACTA元素使用“剪切和粘贴”机制进行转置,DDE转座酶促进了这种机制的进行。尽管CACTA元件具有保守的功能,但它们的DDE转座酶在各个CACTA家族中仍具有不同的外显子数量。虽然较早的研究分析了DDE转座酶的祖先历史,但尚无研究从外在驱动力的变化来研究外显子的丢失和增加。结果我们分析了单子叶和双子叶宿主物种中来自不同CACTA家族的64个转座酶。外显子/内含子边界的注释显示范围为一到六个外显子。建立了基于其蛋白质序列的64个转座酶的稳健的多序列比对,并将其用于系统发育分析,揭示了八个不同的进化枝。我们观察到,CACTA转座酶中的外显子数目对宿主基因组不是特异性的。我们发现,古代的CACTA谱系在单子叶植物和双子叶植物之前就已经发散了。在所有转座酶的三个不同区域中发现了大多数外显子/内含子边界,将63个保守的内含子/外显子边界分组。结论我们提出了一个祖先CACTA转座酶基因模型,该模型由四个外显子组成,该模型早于单子叶植物和双子叶植物的差异。基于此模型,我们提出内含子丢失或获得的途径,以解释观察到的外显子数量变异。尽管内含子丢失似乎占了上风,但仍观察到一个假定的内含子增益案例。

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