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A novel RNA pentaloop fold involved in targeting ADAR2

机译:靶向ADAR2的新型RNA五倍体折叠

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Adenosine deaminases that act on RNA (ADARs) catalyze the site-specific conversion of adenosine to inosine in primary mRNA transcripts, thereby affecting coding potential of mature mRNAs. Structural determinants that define the adenosine moieties for specific ADARs-mediated deaminations are currently unknown. We report the solution structure of the central region of the human R/G stem-loop pre-mRNA, a natural ADAR2 substrate encoding the subunit B of the glutamate receptor (R/G site). The structure reveals that the GCU(A/C)A pentaloop that is conserved in mammals and birds adopts a novel fold. The fold is stabilized by a complex interplay of hydrogen bonds and stacking interactions. We propose that this new pentaloop structure is an important determinant of the R/G site recognition by ADAR2.
机译:作用于RNA(ADAR)的腺苷脱氨基酶催化主要mRNA转录物中腺苷向肌苷的位点特异性转化,从而影响成熟mRNA的编码潜力。目前尚不清楚用于确定特定ADARs介导的脱氨反应的腺苷部分的结构决定簇。我们报告了人类R / G茎环前mRNA,编码谷氨酸受体(R / G站点)的亚基B的天然ADAR2底物的中央区域的解决方案结构。该结构表明,在哺乳动物和鸟类中保守的GCU(A / C)A五倍体采用新的折叠方式。折叠通过氢键和堆积相互作用的复杂相互作用而稳定。我们建议这种新的五人制结构是ADAR2识别R / G站点的重要决定因素。

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