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首页> 外文期刊>Molecular and Cellular Biology >Analysis of Sequence and Structural Features That Identify the B/C Motif of U3 Small Nucleolar RNA as the Recognition Site for the Snu13p-Rrp9p Protein Pair
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Analysis of Sequence and Structural Features That Identify the B/C Motif of U3 Small Nucleolar RNA as the Recognition Site for the Snu13p-Rrp9p Protein Pair

机译:识别U3小核RNA B / C基序作为Snu13p-Rrp9p蛋白对识别位点的序列和结构特征的分析

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The eukaryal Snu13p/15.5K protein binds K-turn motifs in U4 snRNA and snoRNAs. Two Snu13p/15.5K molecules bind the nucleolar U3 snoRNA required for the early steps of preribosomal processing. Binding of one molecule on the C′/D motif allows association of proteins Nop1p, Nop56p, and Nop58p, whereas binding of the second molecule on the B/C motif allows Rrp9p recruitment. To understand how the Snu13p-Rrp9p pair recognizes the B/C motif, we first improved the identification of RNA determinants required for Snu13p binding by experiments using the systematic evolution of ligands by exponential enrichment. This demonstrated the importance of a U·U pair stacked on the sheared pairs and revealed a direct link between Snu13p affinity and the stability of helices I and II. Sequence and structure requirements for efficient association of Rrp9p on the B/C motif were studied in yeast cells by expression of variant U3 snoRNAs and immunoselection assays. A G-C pair in stem II, a G residue at position 1 in the bulge, and a short stem I were found to be required. The data identify the in vivo function of most of the conserved residues of the U3 snoRNA B/C motif. They bring important information to understand how different K-turn motifs can recruit different sets of proteins after Snu13p association.
机译:真核Snu13p / 15.5K蛋白与U4 snRNA和snoRNA中的K-turn母题结合。两个Snu13p / 15.5K分子结合核糖体前加工的早期步骤所需的核仁U3 snoRNA。 C'/ D基序上的一个分子的结合允许蛋白Nop1p,Nop56p和Nop58p结合,而B / C基序上的第二个分子的结合则允许Rrp9p募集。为了了解Snu13p-Rrp9p对如何识别B / C基序,我们首先通过使用通过指数富集的配体系统进化的实验,改进了Snu13p结合所需的RNA决定簇的鉴定。这证明了在剪切对上堆积U·U对的重要性,并揭示了Snu13p亲和力与螺旋I和II的稳定性之间的直接联系。通过变异U3 snoRNA的表达和免疫选择分析,研究了酵母细胞中Rrp9p在B / C基序上有效结合的序列和结构要求。发现茎II中有一个G-C对,凸起中第1位的G残基和一个短茎I。数据确定了U3 snoRNA B / C基序的大多数保守残基的体内功能。他们带来了重要的信息,以了解Snu13p缔合后不同的K-turn基序如何募集不同的蛋白质。

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