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Non-LTR R2 Element Evolutionary Patterns: Phylogenetic Incongruences, Rapid Radiation and the Maintenance of Multiple Lineages

机译:非LTR R2元素进化模式:系统发育不一致,快速辐射和多个谱系的维持。

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摘要

Retrotransposons of the R2 superclade specifically insert within the 28S ribosomal gene. They have been isolated from a variety of metazoan genomes and were found vertically inherited even if their phylogeny does not always agree with that of the host species. This was explained with the diversification/extinction of paralogous lineages, being proved the absence of horizontal transfer. We here analyze the widest available collection of R2 sequences, either newly isolated from recently sequenced genomes or drawn from public databases, in a phylogenetic framework. Results are congruent with previous analyses, but new important issues emerge. First, the N-terminal end of the R2-B clade protein, so far unknown, presents a new zinc fingers configuration. Second, the phylogenetic pattern is consistent with an ancient, rapid radiation of R2 lineages: being the estimated time of R2 origin (850–600 Million years ago) placed just before the metazoan Cambrian explosion, the wide element diversity and the incongruence with the host phylogeny could be attributable to the sudden expansion of available niches represented by host’s 28S ribosomal genes. Finally, we detect instances of coexisting multiple R2 lineages showing a non-random phylogenetic pattern, strongly similar to that of the “library” model known for tandem repeats: a collection of R2s were present in the ancestral genome and then differentially activated/repressed in the derived species. Models for activation/repression as well as mechanisms for sequence maintenance are also discussed within this framework.
机译:R2超融合的逆转座子特异地插入28S核糖体基因内。它们已从多种后生动物基因组中分离出来,即使它们的系统发育并不总是与宿主物种一致,也被发现是垂直遗传的。这可以通过旁系血统的多样化/消灭来解释,事实证明没有水平转移。在这里,我们在系统发育分析框架中分析最广泛的R2序列集合,这些序列是从最近测序的基因组中新分离的,或者是从公共数据库中提取的。结果与以前的分析一致,但是出现了新的重要问题。首先,迄今未知的R2-B进化枝蛋白的N末端呈现出新的锌指构型。第二,系统发育模式与古老,快速的R2谱系辐射相一致:是R2起源的估计时间(850-600百万年前),恰好在后生寒武纪爆发之前,广泛的元素多样性以及与宿主的不一致系统发育可归因于以宿主的28S核糖体基因为代表的可利用生态位的突然扩展。最后,我们检测到多个R2谱系共存的实例,这些谱系显示出非随机的系统发育模式,与串联重复已知的“图书馆”模型非常相似:祖先基因组中存在一组R2,然后在它们中进行差异激活/抑制衍生物种。在该框架内还讨论了激活/抑制模型以及序列维持机制。

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