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Convergent intron gains in hymenopteran elongation factor-1α

机译:膜翅目延伸因子-1α的收敛内含子获得

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The eukaryotic translation elongation factor-1α gene (eEF1A) has been used extensively in higher level phylogenetics of insects and other groups, despite being present in two or more copies in several taxa. Orthology assessment has relied heavily on the position of introns, but the basic assumption of low rates of intron loss and absence of convergent intron gains has not been tested thoroughly. Here, we study the evolution of eEF1A based on a broad sample of taxa in the insect order Hymenoptera. The gene is universally present in two copies - F1 and F2 - both of which apparently originated before the emergence of the order. An elevated ratio of non-synonymous versus synonymous substitutions and differences in rates of amino acid replacements between the copies suggest that they evolve independently, and phylogenetic methods clearly cluster the copies separately. The F2 copy appears to be ancient; it is orthologous with the copy known as F1 in Diptera, and is likely present in most insect orders. The hymenopteran F1 copy, which may or may not be unique to this order, apparently originated through retroposition and was originally intron free. During the evolution of the Hymenoptera, it has successively accumulated introns, at least three of which have appeared at the same position as introns in the F2 copy or in eEF1A copies in other insects. The sites of convergent intron gain are characterized by highly conserved nucleotides that strongly resemble specific intron-associated sequence motifs, so-called proto-splice sites. The significant rate of convergent intron gain renders intron-exon structure unreliable as an indicator of orthology in eEF1A, and probably also in other protein-coding genes.
机译:真核翻译延伸因子-1α基因(eEF1A)已在昆虫和其他群体的更高系统发育学中广泛使用,尽管在多个分类群中有两个或多个拷贝存在。矫形学评估在很大程度上依赖于内含子的位置,但是对内含子丢失率低和缺乏会聚内含子增益的基本假设尚未进行充分的测试。在这里,我们基于昆虫纲膜翅目中广泛的分类单元样本研究eEF1A的进化。该基因普遍存在于两个拷贝中-F1和F2-两者显然是在该命令出现之前起源的。非同义替换与同义替换的比例增加,以及副本之间氨基酸替换率的差异表明它们独立进化,并且系统发育方法清楚地将副本分别聚类。 F2副本看起来很古老;它与双翅目中的F1直系同源,并且可能存在于大多数昆虫纲中。膜翅目F1拷贝,可能是也可能不是该顺序的唯一拷贝,显然是通过逆转录产生的,最初是无内含子的。在膜翅目的进化过程中,它连续积累了内含子,其中至少三个与F2拷贝或其他昆虫的eEF1A拷贝中的内含子出现在同一位置。收敛的内含子获得位点的特征是高度保守的核苷酸,其与特定的内含子相关的序列基序非常相似,即所谓的原始剪接位点。收敛的内含子增益的显着速率使得内含子-外显子结构在eEF1A以及其他蛋白质编码基因中作为正交学指标不可靠。

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