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Structural insights into the targeting of mRNA GU-rich elements by the three RRMs of CELF1

机译:CELF1的三个RRM靶向靶向富含GU的mRNA的结构见解

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The CUG-BP, Elav-like family (CELF) of RNA-binding proteins control gene expression at a number of different levels by regulating pre-mRNA splicing, deadenylation and mRNA stability. We present structural insights into the binding selectivity of CELF member 1 (CELF1) for GU-rich mRNA target sequences of the general form 5'-UGUN(x)UGUN(y)UGU and identify a high affinity interaction (K-d similar to 100 nM for x = 2 and y = 4) with simultaneous binding of all three RNA recognition motifs within a single 15-nt binding element. RNA substrates spin-labelled at either the 3' or 5' terminus result in differential nuclear magnetic resonance paramagnetic relaxation enhancement effects, which are consistent with a non-sequential 2-1-3 arrangement of the three RNA recognition motifs on UGU sites in a 5' to 3' orientation along the RNA target. We further demonstrate that CELF1 binds to dispersed single-stranded UGU sites at the base of an RNA hairpin providing a structural rationale for recognition of CUG expansion repeats and splice site junctions in the regulation of alternative splicing.
机译:RNA结合蛋白的CUG-BP,Elav样家族(CELF)通过调节前mRNA剪接,腺苷酸化和mRNA稳定性来控制许多不同水平的基因表达。我们目前的结构见解的CELF成员1(CELF1)对GU富mRNA靶序列的一般形式5'-UGUN(x)UGUN(y)UGU的结合选择性,并鉴定出高亲和力相互作用(Kd类似于100 nM (对于x = 2和y = 4),同时在单个15-nt结合元件中同时结合所有三个RNA识别基序。在3'或5'末端自旋标记的RNA底物导致差异的核磁共振顺磁弛豫增强效应,这与UGU位​​点中三个UGU识别基序的非顺序2-1-3排列相一致。沿着RNA靶标的5'至3'方向。我们进一步证明,CELF1在RNA发夹的底部与分散的单链UGU位点结合,为识别CUG扩展重复和剪接位点连接提供了结构合理的剪接调控。

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