Burke William D, Singh Daljit, Eickbush Thomas H
Department of Biology, University of Rochester, USA.
Mol Biol Evol. 2003 Aug;20(8):1260-70. doi: 10.1093/molbev/msg141. Epub 2003 May 30.
A small (100 bp) region of the 28S rRNA gene has been shown to serve as the target site for the insertion of non-long terminal repeat (non-LTR) retrotransposons in both arthropods and nematodes. Here we characterize a lineage of non-LTR retrotransposons that inserts into this target site in the phylum Platyhelminthes. Dugesiid planaria contain elements, named R5, that insert 8 bp upstream of the target site used by arthropod R2 elements. The complete sequence of this element from Girardia tigrina revealed that it encoded two open reading frames (ORFs). The second ORF contained reverse transcriptase and restriction enzyme-like endonuclease domains similar to those found in R2 and R4, the elements that insert into the 28S genes of nematodes. The closest relative of R5, however, was the element NeSL-1, which inserts into the spliced leader 1 exons of nematodes. The rRNA genes of dugesiid planaria are unusual in that they comprise two types of rDNA units that differ by 8%-10% in nucleotide sequence of the 18S and 28S coding regions. Type II units are transcribed in adult tissues at levels that are less than 1% that of the type I units. R5 elements were only found inserted in the type II units, where presumably they cause less harm to the host. A second unusual aspect of the dugesiid rRNA genes is that the target site for the R5 insertion is duplicated 300 bp upstream of the original insertion site. R5 elements were identified at both sites. These findings expand the distribution of non-LTR elements that are specialized for insertion into the 28S gene and suggest that still more elements exist in other eukaryotic taxa. Attempts to trace the phylogeny of R5 did not offer sufficient resolution to determine whether R2, R4, and R5 represent the same lineage or whether they represent independent specializations for the 28S gene.
28S rRNA基因的一个小区域(100个碱基对)已被证明是节肢动物和线虫中非长末端重复(non-LTR)逆转座子插入的靶位点。在这里,我们描述了一类在扁形动物门中插入该靶位点的非LTR逆转座子。真涡虫含有名为R5的元件,它们插入节肢动物R2元件所使用靶位点上游8个碱基对处。来自虎纹涡虫的该元件的完整序列显示,它编码两个开放阅读框(ORF)。第二个ORF包含与在插入线虫28S基因的元件R2和R4中发现的类似的逆转录酶和限制性内切酶样结构域。然而,R5最接近的亲属是插入线虫剪接前导序列1外显子的元件NeSL-1。真涡虫的rRNA基因不同寻常之处在于它们由两种类型的rDNA单元组成,这两种单元在18S和28S编码区的核苷酸序列上相差8%-10%。II型单元在成体组织中的转录水平不到I型单元的1%。R5元件仅在II型单元中被发现插入,据推测它们对宿主造成的危害较小。真涡虫rRNA基因的另一个不同寻常之处在于,R5插入的靶位点在原始插入位点上游300个碱基对处被重复。在这两个位点都鉴定到了R5元件。这些发现扩展了专门插入28S基因的非LTR元件的分布,并表明在其他真核生物类群中可能存在更多此类元件。追踪R5系统发育的尝试没有提供足够的分辨率来确定R2、R4和R5是否代表同一谱系,或者它们是否代表对28S基因的独立特化。