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Box H and Box ACA Are Nucleolar Localization Elements of U17 Small Nucleolar RNA

机译:框H和框ACA是U17小核仁RNA的核仁定位元件

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摘要

The nucleolar localization elements (NoLEs) of U17 small nucleolar RNA (snoRNA), which is essential for rRNA processing and belongs to the box H/ACA snoRNA family, were analyzed by fluorescence microscopy. Injection of mutant U17 transcripts into Xenopus laevis oocyte nuclei revealed that deletion of stems 1, 2, and 4 of U17 snoRNA reduced but did not prevent nucleolar localization. The deletion of stem 3 had no adverse effect. Therefore, the hairpins of the hairpin–hinge–hairpin–tail structure formed by these stems are not absolutely critical for nucleolar localization of U17, nor are sequences within stems 1, 3, and 4, which may tether U17 to the rRNA precursor by base pairing. In contrast, box H and box ACA are major NoLEs; their combined substitution or deletion abolished nucleolar localization of U17 snoRNA. Mutation of just box H or just the box ACA region alone did not fully abolish the nucleolar localization of U17. This indicates that the NoLEs of the box H/ACA snoRNA family function differently from the bipartite NoLEs (conserved boxes C and D) of box C/D snoRNAs, where mutation of either box alone prevents nucleolar localization.
机译:通过荧光显微镜分析了U17小核仁RNA(snoRNA)的核仁定位元件(NoLEs),这对rRNA加工至关重要,属于盒H / ACA snoRNA家族。将突变的U17转录物注入非洲爪蟾卵母细胞核显示,U17 snoRNA茎1、2和4的缺失减少,但并未阻止核仁定位。茎3的删除没有不利影响。因此,由这些茎形成的发夹-铰链-发夹-尾巴结构的发夹对于U17的核仁定位不是绝对关键,茎1、3和4中的序列也不是必不可少的,它们可能通过碱基将U17束缚到rRNA前体配对。相反,H框和ACA框是主要的NoLE。它们的组合取代或缺失消除了U17 snoRNA的核仁定位。仅框H或框ACA区域的单独突变并未完全消除U17的核仁定位。这表明盒H / ACA snoRNA家族的NoLEs与盒C / D snoRNA的二部NoLE(保守的盒C和D)的功能不同,后者单独突变一个盒可防止核仁定位。

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