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The making of a genomic parasite - the Mothra family sheds light on the evolution of Helitrons in plants

机译:基因组寄生虫的产生-Mothra家族揭示了植物中Helitron的进化

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Helitrons are Class II transposons which are highly abundant in almost all eukaryotes. However, most Helitrons lack protein coding sequence. These non-autonomous elements are thought to hijack recombinase/helicase (RepHel) and possibly further enzymes from related, autonomous elements. Interestingly, many plant Helitrons contain an additional gene encoding a single-strand binding protein homologous to Replication Factor A (RPA), a highly conserved, single-copy gene found in all eukaryotes. Here, we describe the analysis of DHH_Mothra, a high-copy non-autonomous Helitron in the genome of rice (Oryza sativa). Mothra has a low GC-content and consists of two distinct blocs of tandem repeats. Based on homology between their termini, we identified a putative mother element which encodes an RPA-like protein but has no RepHel gene. Additionally, we found a putative autonomous sister-family with strong homology to the Mothra mother element in the RPA protein and terminal sequences, which we propose provides the RepHel domain for the Mothra family. Furthermore, we phylogenetically analyzed the evolutionary history of RPA-like proteins. Interestingly, plant Helitron RPAs (PHRPAs) are only found in monocotyledonous and dicotyledonous plants and they form a monophyletic group which branched off before the eukaryotic “core” RPAs. Our data show how erosion of autonomous Helitrons can lead to different “levels” of autonomy within Helitron families and can create highly successful subfamilies of non-autonomous elements. Most importantly, our phylogenetic analysis showed that the PHRPA gene was most likely acquired via horizontal gene transfer from an unknown eukaryotic donor at least 145–300 million years ago in the common ancestor of monocotyledonous and dicotyledonous plants. This might have led to the evolution of a separate branch of the Helitron superfamily in plants.
机译:Helitrons是II类转座子,几乎在所有真核生物中都非常丰富。但是,大多数Helitrons缺乏蛋白质编码序列。这些非自主元件被认为劫持了重组酶/解旋酶(RepHel),并可能劫持了来自相关自主元件的其他酶。有趣的是,许多植物Helitrons包含一个额外的基因,该基因编码与复制因子A(RPA)同源的单链结合蛋白,RPA是在所有真核生物中发现的高度保守的单拷贝基因。在这里,我们描述了DHH_Mothra的分析,DHH_Mothra是水稻(Oryza sativa)基因组中的一种高拷贝非自主性Helitron。 Mothra的GC含量低,由两个不同的串联重复序列组成。基于它们的末端之间的同源性,我们确定了一个假定的母亲元件,该元件编码RPA样蛋白,但没有RepHel基因。此外,我们发现了一个推定的自治姐妹家族,与RPA蛋白和末端序列中的Mothra母亲元件具有很强的同源性,我们建议为Mothra家族提供RepHel域。此外,我们系统地分析了RPA样蛋白的进化历史。有趣的是,植物Helitron RPA(PHRPA)仅在单子叶和双子叶植物中发现,它们形成了一个单系群,在真核“核心” RPA之前分支。我们的数据显示,自主直升机的侵蚀会如何导致直升机家族内部不同程度的自主,并能够创建非自主元素的高度成功的子家族。最重要的是,我们的系统发育分析表明,至少在145-3亿年前,在单子叶和双子叶植物的共同祖先中,PHRPA基因很可能是通过水平基因转移从未知的真核生物供体中获得的。这可能导致了Helitron超家族的一个独立分支在植物中的进化。

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