Gogvadze Elena, Barbisan Crystel, Lebrun Marc-Henri, Buzdin Anton
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow 117871, Russia.
BMC Genomics. 2007 Oct 8;8:360. doi: 10.1186/1471-2164-8-360.
A systematic survey of loci carrying retrotransposons in the genome of the rice blast fungus Magnaporthe grisea allowed the identification of novel non-canonical retropseudogenes. These elements are chimeric retrogenes composed of DNA copies from different cellular transcripts directly fused to each other. Their components are copies of a non protein-coding highly expressed RNA of unknown function termed WEIRD and of two fungal retrotransposons: MGL and Mg-SINE. Many of these chimeras are transcribed in various M. grisea tissues and during plant infection. Chimeric retroelements with a similar structure were recently found in three mammalian genomes. All these chimeras are likely formed by RNA template switches during the reverse transcription of diverse LINE elements.
We have shown that in M. grisea template switching occurs at specific sites within the initial template RNA which contains a characteristic consensus sequence. We also provide evidence that both single and double template switches may occur during LINE retrotransposition, resulting in the fusion of three different transcript copies. In addition to the 33 bipartite elements, one tripartite chimera corresponding to the fusion of three retrotranscripts (WEIRD, Mg-SINE, MGL-LINE) was identified in the M. grisea genome. Unlike the previously reported two human tripartite elements, this fungal retroelement is flanked by identical 14 bp-long direct repeats. The presence of these short terminal direct repeats demonstrates that the LINE enzymatic machinery was involved in the formation of this chimera and its integration in the M. grisea genome.
A survey of mammalian genomic databases also revealed two novel tripartite chimeric retroelements, suggesting that double template switches occur during reverse transcription of LINE retrotransposons in different eukaryotic organisms.
对稻瘟病菌Magnaporthe grisea基因组中携带逆转座子的位点进行系统调查,发现了新型非典型逆转假基因。这些元件是嵌合逆转基因,由来自不同细胞转录本的DNA拷贝直接相互融合而成。它们的组成部分是一种功能未知的非蛋白质编码高表达RNA(称为WEIRD)的拷贝,以及两种真菌逆转座子:MGL和Mg-SINE。许多这些嵌合体在稻瘟病菌的各种组织中以及植物感染过程中都有转录。最近在三个哺乳动物基因组中发现了具有相似结构的嵌合逆转元件。所有这些嵌合体可能是在不同LINE元件逆转录过程中通过RNA模板转换形成的。
我们已经表明,在稻瘟病菌中,模板转换发生在初始模板RNA内的特定位点,该位点包含一个特征性共有序列。我们还提供证据表明,在LINE逆转座过程中可能发生单模板转换和双模板转换,导致三个不同转录本拷贝的融合。除了33个二分体元件外,在稻瘟病菌基因组中还鉴定出一个对应于三个逆转录转录本(WEIRD、Mg-SINE、MGL-LINE)融合的三分体嵌合体。与之前报道的两个人类三分体元件不同,这种真菌逆转元件两侧是相同的14 bp长的直接重复序列。这些短末端直接重复序列的存在表明,LINE酶机制参与了该嵌合体的形成及其在稻瘟病菌基因组中的整合。
对哺乳动物基因组数据库的调查还揭示了两个新型三分体嵌合逆转元件,表明在不同真核生物中LINE逆转座子逆转录过程中会发生双模板转换。