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Computational screen for spliceosomal RNA genes aids in defining the phylogenetic distribution of major and minor spliceosomal components

机译:剪接RNA基因的计算机筛选有助于确定主要和次要剪接成分的系统发育分布

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The RNA molecules of the spliceosome are critical for specificity and catalysis during splicing of eukaryotic pre-mRNA. In order to examine the evolution and phylogenetic distribution of these RNAs, we analyzed 149 eukaryotic genomes representing a broad range of phylogenetic groups. RNAs were predicted using high-sensitivity local alignment methods and profile HMMs in combination with covariance models. The results provide the most comprehensive view so far of the phylogenetic distribution of spliceosomal RNAs. RNAs were predicted in many phylogenetic groups where these RNA were not previously reported. Examples are RNAs of the major (U2-type) spliceosome in all fungal lineages, in lower metazoa and many protozoa. We also identified the minor (U12-type) spliceosomal U11 and U6atac RNAs in Acanthamoeba castellanii, where U12 spliceosomal RNA as well as minor introns were reported recently. In addition, minor-spliceosome-specific RNAs were identified in a number of phylogenetic groups where previously such RNAs were not observed, including the nematode Trichinella spiralis, the slime mold Physarum polycephalum and the fungal lineages Zygomycota and Chytridiomycota. The detailed map of the distribution of the U12-type RNA genes supports an early origin of the minor spliceosome and points to a number of occasions during evolution where it was lost.
机译:剪接体的RNA分子对于真核pre-mRNA剪接过程中的特异性和催化作用至关重要。为了检查这些RNA的进化和系统发育分布,我们分析了149个真核生物基因组,它们代表了广泛的系统发育群体。使用高灵敏度的局部比对方法和结合协方差模型的HMM轮廓预测RNA。结果提供了迄今为止最广泛的剪接体RNA系统发育分布的观点。在以前没有报道过这些RNA的许多系统发育组中都预测到了RNA。实例是所有真菌谱系,后生后级和许多原生动物中主要(U2型)剪接体的RNA。我们还确定了小(U12型)剪接的U11和U6atac RNAs在棘阿米巴castellanii,那里最近报道了U12剪接RNA和小内含子。另外,在许多以前没有观察到此类RNA的系统发育组中鉴定了次剪接体特异性RNA,包括线虫旋毛虫​​,粘液菌多头cephal,真菌谱系Zygomycota和Chytridiomycota。 U12型RNA基因分布的详细图谱支持了次剪接体的早期起源,并指出了在进化过程中多次丢失的情况。

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