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Characteristics of inteins in invertebrate iridoviruses and factors controlling insertion in their viral hosts

机译:无脊椎动物虹膜病毒中内含子的特征及控制其病毒宿主插入的因素

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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.
机译:内含蛋白是自剪接蛋白,其在宿主编码的蛋白内符合读框。编码内含蛋白的DNA元件特别插入靶基因高度保守的基序中。这些可移动的遗传成分分布不均,到目前为止,仅在某些细菌,古细菌和真菌,藻类和变形虫的一些病毒以及昆虫病原体Chilo虹彩病毒(CIV)中发现。在这里,我们报告发现了七种新的内含蛋白,它们寄生于感染后生动物的虹膜病毒:三个位于其δDNA聚合酶基因内,四个位于编码其大核糖核苷酸还原酶亚基的基因内。编码序列分析表明,这些内含蛋白是由祖先获得的,这些祖先由目前被归类为具有大双链(ds)DNA基因组的不同病毒家族成员的病毒共享,然后通过垂直传播得以维持或丢失。与在其他病毒和原核生物中发现的内含子相比,在虹膜病毒的δDNA聚合酶中存在的内含子在不同的位置插入YGDTDS基序,这一发现引起了人们的极大兴趣。此外,我们的系统发育研究表明,这些病毒的δDNA聚合酶中存在的内含蛋白的来源可能与原核生物不同。最后,我们使用宿主基因中内含子插入位点的序列特征来讨论病毒种内和间的内含子高度多态性及其在这些病毒的真核宿主中其遗传对应物的免疫力。

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