Roffler Stefan, Menardo Fabrizio, Wicker Thomas
Institute of Plant Biology, University of Zürich, Zollikerstrasse 107, Zürich, CH-8008 Switzerland.
Mob DNA. 2015 Dec 17;6:23. doi: 10.1186/s13100-015-0054-4. eCollection 2015.
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.
Helitrons是II类转座子,在几乎所有真核生物中都高度丰富。然而,大多数Helitrons缺乏蛋白质编码序列。这些非自主元件被认为会从相关的自主元件中劫持重组酶/解旋酶(RepHel)以及可能的其他酶。有趣的是,许多植物Helitrons包含一个额外的基因,该基因编码一种与复制因子A(RPA)同源的单链结合蛋白,RPA是在所有真核生物中都存在的高度保守的单拷贝基因。
在这里,我们描述了对水稻(Oryza sativa)基因组中一个高拷贝非自主Helitron——DHH_Mothra的分析。Mothra的GC含量较低,由两个不同的串联重复序列块组成。基于其末端之间的同源性,我们鉴定出一个推定的母元件,它编码一种类似RPA的蛋白,但没有RepHel基因。此外,我们发现了一个推定的自主姐妹家族,其在RPA蛋白和末端序列上与Mothra母元件具有很强的同源性,我们认为它为Mothra家族提供了RepHel结构域。此外,我们对类似RPA蛋白的进化历史进行了系统发育分析。有趣的是,植物Helitron RPA(PHRPA)仅在单子叶植物和双子叶植物中发现,它们形成一个单系类群,在真核生物“核心”RPA之前分支出来。
我们的数据显示了自主Helitrons的侵蚀如何导致Helitron家族内不同“程度”的自主性,并能产生非常成功的非自主元件亚家族。最重要的是,我们的系统发育分析表明,PHRPA基因很可能是在至少1.45 - 3亿年前通过水平基因转移从一个未知的真核生物供体那里获得的,发生在单子叶植物和双子叶植物的共同祖先中。这可能导致了植物中Helitron超家族一个独立分支的进化。