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Basis of altered RNA-binding specificity by PUF proteins revealed by crystal structures of yeast Puf4p

机译:酵母Puf4p晶体结构揭示PUF蛋白改变RNA结合特异性的基础

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摘要

Pumilio/FBF (PUF) family proteins are found in eukaryotic organisms and regulate gene expression post-transcriptionally by binding to sequences in the 3' untranslated region of target transcripts. PUF proteins contain an RNA binding domain that typically comprises eight alpha-helical repeats, each of which recognizes one RNA base. Some PUF proteins, including yeast Puf4p, have altered RNA binding specificity and use their eight repeats to bind to RNA sequences with nine or ten bases. Here we report the crystal structures of Puf4p alone and in complex with a 9-nucleotide (nt) target RNA sequence, revealing that Puf4p accommodates an 'extra' nucleotide by modest adaptations allowing one base to be turned away from the RNA binding surface. Using structural information and sequence comparisons, we created a mutant Puf4p protein that preferentially binds to an 8-nt target RNA sequence over a 9-nt sequence and restores binding of each protein repeat to one RNA base.
机译:在真核生物中发现了Pumilio / FBF(PUF)家族蛋白,并通过与靶标转录本的3'非翻译区中的序列结合来转录后调节基因表达。 PUF蛋白质包含一个RNA结合结构域,该结构域通常包含八个α-螺旋重复序列,每个重复序列识别一个RNA碱基。一些PUF蛋白,包括酵母Puf4p,已经改变了RNA结合特异性,并使用其8个重复序列与9个或10个碱基的RNA序列结合。在这里,我们报告了单独的Puf4p的晶体结构以及与9个核苷酸(nt)靶RNA序列复合的晶体结构,揭示了Puf4p通过适度的适应作用容纳了一个“额外的”核苷酸,从而使一个碱基可以从RNA结合表面上移开。使用结构信息和序列比较,我们创建了一个突变的Puf4p蛋白,该蛋白优先结合9nt序列的8nt靶RNA序列,并恢复每种蛋白重复序列​​与一个RNA碱基的结合。

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