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Pseudouridine modification in Caenorhabditis elegans spliceosomal snRNAs: unique modifications are found in regions involved in snRNA-snRNA interactions

机译:秀丽隐杆线虫剪接体snRNA中的假性尿苷修饰:在涉及snRNA-snRNA相互作用的区域中发现独特的修饰

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Background Pseudouridine (Ψ) is an abundant modified nucleoside in RNA and a number of studies have shown that the presence of Ψ affects RNA structure and function. The positions of Ψ in spliceosomal small nuclear RNAs (snRNAs) have been determined for a number of species but not for the snRNAs from Caenorhabditis elegans (C. elegans), a popular experimental model system of development. Results As a prelude to determining the function of or requirement for this modification in snRNAs, we have mapped the positions of Ψ in U1, U2, U4, U5, and U6 snRNAs from worms using a specific primer extension method. As with other species, C. elegans U2 snRNA has the greatest number of Ψ residues, with nine, located in the 5' half of the U2 snRNA. U5 snRNA has three Ψs, in or near the loop of the large stem-loop that dominates the structure of this RNA. U6 and U1 snRNAs each have one Ψ, and two Ψ residues were found in U4 snRNA. Conclusion The total number of Ψs found in the snRNAs of C. elegans is significantly higher than the minimal amount found in yeasts but it is lower than that seen in sequenced vertebrate snRNAs. When the actual sites of modification on C. elegans snRNAs are compared with other sequenced snRNAs most of the positions correspond to modifications found in other species. However, two of the positions modified on C. elegans snRNAs are unique, one at position 28 on U2 snRNA and one at position 62 on U4 snRNA. Both of these modifications are in regions of these snRNAs that interact with U6 snRNA either in the spliceosome or in the U4/U6 small nuclear ribonucleoprotein particle (snRNP) and the presence of Ψ may be involved in strengthening the intermolecular association of the snRNAs.
机译:背景假性尿苷(Ψ)是RNA中大量修饰的核苷,许多研究表明Ψ的存在会影响RNA的结构和功能。已经确定了许多物种中剪接体小核RNA(snRNA)中of的位置,但尚未确定秀丽隐杆线虫(C. elegans)(一种流行的实验开发系统)中的snRNA的位置。结果作为确定snRNA中这种修饰的功能或要求的先驱,我们已使用特定引物延伸方法绘制了蠕虫在U1,U2,U4,U5和U6 snRNA中Ψ的位置。与其他物种一样,秀丽隐杆线虫的U2 snRNA残基数量最多,其中9个位于U2 snRNA的5'一半。 U5 snRNA在其主干结构的大茎环的环中或附近具有三个。 U6和U1 snRNA各自具有1个,在U4 snRNA中发现2个残基。结论在秀丽隐杆线虫的snRNA中发现的Ψs总数明显高于在酵母中发现的最小数量,但低于在测序的脊椎动物snRNA中发现的数量。当将秀丽隐杆线虫的snRNA的实际修饰位点与其他测序的snRNA进行比较时,大多数位置对应于其他物种中发现的修饰。但是,秀丽隐杆线虫snRNA上修饰的两个位置是唯一的,一个位于U2 snRNA的28位,另一个位于U4 snRNA的62位。这两个修饰都在这些snRNA的区域中,该区域在剪接体中或在U4 / U6小核糖核糖蛋白颗粒(snRNP)中与U6 snRNA相互作用,并且Ψ的存在可能与加强snRNA的分子间结合有关。

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