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Nucleolar Localization Elements of Xenopus laevis U3 Small Nucleolar RNA

机译:非洲爪蟾U3小核仁RNA的核仁定位元件

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摘要

The Nucleolar Localization Elements (NoLEs) of Xenopus laevis U3 small nucleolar RNA (snoRNA) have been defined. Fluorescein-labeled wild-type U3 snoRNA injected into Xenopus oocyte nuclei localized specifically to nucleoli as shown by fluorescence microscopy. Injection of mutated U3 snoRNA revealed that the 5′ region containing Boxes A and A′, known to be important for rRNA processing, is not essential for nucleolar localization. Nucleolar localization of U3 snoRNA was independent of the presence and nature of the 5′ cap and the terminal stem. In contrast, Boxes C and D, common to the Box C/D snoRNA family, are critical elements for U3 localization. Mutation of the hinge region, Box B, or Box C′ led to reduced U3 nucleolar localization. Results of competition experiments suggested that Boxes C and D act in a cooperative manner. It is proposed that Box B facilitates U3 snoRNA nucleolar localization by the primary NoLEs (Boxes C and D), with the hinge region of U3 subsequently base pairing to the external transcribed spacer of pre-rRNA, thus positioning U3 snoRNA for its roles in rRNA processing.
机译:非洲爪蟾U3小核仁RNA(snoRNA)的核仁定位元件(NoLEs)已被定义。荧光显微镜显示,荧光素标记的野生型U3 snoRNA注射到非洲爪蟾卵母细胞核中后,特异性定位在核仁上。注射突变的U3 snoRNA后发现,含有Box A和A'的5'区域对rRNA的加工很重要,但对核仁定位不是必需的。 U3 snoRNA的核仁定位独立于5'帽和末端茎的存在和性质。相反,Box C / D snoRNA家族共有的Box C和D是U3定位的关键要素。铰链区,框B或框C'的突变导致U3核仁定位降低。竞争实验的结果表明,方框C和方框D相互配合。建议框B通过主要NoLE(框C和D)促进U3 snoRNA核仁定位,随后U3的铰链区与pre-rRNA的外部转录间隔区碱基配对,从而将U3 snoRNA定位于其在rRNA中的作用处理。

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