UMR INRA-CNRS 7247, PRC, Centre INRA de Nouzilly, 37380 Nouzilly, France.
Mol Phylogenet Evol. 2013 Apr;67(1):246-54. doi: 10.1016/j.ympev.2013.01.017. Epub 2013 Feb 7.
Inteins are self-splicing proteins that occur in-frame within host-coded proteins. DNA elements coding for inteins insert specifically in highly conserved motifs of target genes. These mobile genetic elements have an uneven distribution and thus far have been found only in certain species of bacteria, archaea and fungi, a few viruses of algae and amoebozoa and in the entomopathogen, Chilo iridescent virus (CIV). Here, we report the discovery of seven new inteins parasitizing iridoviruses infecting metazoans: three within their δ DNA polymerase genes and four in genes coding for their large ribonucleotide reductase subunit. Analyses of coding sequences suggest that these inteins were acquired by ancestors shared by viruses currently classified as members of different families of viruses with large double-stranded (ds) DNA genomes and then were maintained by vertical transmission, or lost. Of significant interest is the finding that inteins present in the δ DNA polymerases of iridoviruses insert at a different location into the YGDTDS motif when compared to those found in other viruses and prokaryotes. In addition, our phylogenetic investigations suggest that inteins present in the δ DNA polymerases of these viruses might have an origin different from those found in prokaryotes. Finally, we use the sequence features of the intein insertion sites in host genes to discuss the high polymorphisms of inteins within and among viral species and the immunity of their genetic counterparts in the eukaryotic hosts of these viruses.
内含子是自我剪接的蛋白质,它们在宿主编码的蛋白质中以框架内的形式出现。编码内含子的 DNA 元件特异性地插入靶基因高度保守的模体中。这些移动遗传元件分布不均匀,迄今为止仅在某些细菌、古细菌和真菌、一些藻类和变形虫的病毒以及昆虫病原体 Chilo iridescent virus (CIV) 中发现。在这里,我们报告了七种新的内含子寄生在感染后生动物的虹彩病毒中的发现:三种在它们的 δ DNA 聚合酶基因中,四种在编码它们的大核糖核苷酸还原酶亚基的基因中。编码序列的分析表明,这些内含子是由目前分类为具有大双链 (ds) DNA 基因组的不同病毒家族成员的病毒的共同祖先获得的,然后通过垂直传播或丢失得以维持。值得注意的是,发现虹彩病毒的 δ DNA 聚合酶中的内含子与在其他病毒和原核生物中发现的内含子相比,在插入 YGDTDS 模体时位于不同的位置。此外,我们的系统发育研究表明,这些病毒的 δ DNA 聚合酶中的内含子可能与原核生物中的内含子起源不同。最后,我们利用宿主基因中内含子插入位点的序列特征,讨论了病毒种内和种间内含子的高度多态性及其在这些病毒的真核宿主中的遗传对应物的免疫性。