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Structural and thermodynamic signatures that define pseudotriloop RNA hairpins

机译:定义伪三环RNA发夹的结构和热力学特征

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Pseudotriloop (PTL) structures in RNAs have been recognized as essential elements in RNA folding and recognition of proteins. PTL structures are derived from hexaloops by formation of a cross-loop base pair leaving a triloop and 3′ bulged out residue. Despite their common presence and functional importance, insufficient structural and thermodynamic data are available that can be used to predict formation of PTLs from sequence alone. Using NMR spectroscopy and UV-melting data we established factors that contribute to the formation and stability of PTL structures derived from hepatitis B virus and human foamy virus. The NMR data show that, besides the cross-loop base pair, also a 3′ pyrimidine bulge and a G -C loop-closing base pair are primary determinants of PTL formation. By changing the G-C closing base pair into C-G, the PTL switches into a hexaloop. Comparison of these rules with regular triloop hairpins and PTLs from other sources is discussed as well as the conservation of a PTL in human foamy virus and other spumaretroviruses.
机译:RNA中的伪三环(PTL)结构已被认为是RNA折叠和蛋白质识别中必不可少的元素。通过形成交叉环碱基对而留下三环和3'突出的残基,从六环衍生出PTL结构。尽管它们普遍存在并且在功能上很重要,但是仍然没有足够的结构和热力学数据可用于仅从序列中预测PTL的形成。使用NMR光谱学和UV熔融数据,我们建立了有助于衍生自乙型肝炎病毒和人泡沫状病毒的PTL结构的形成和稳定性的因素。 NMR数据表明,除了交叉环碱基对之外,3'嘧啶凸起和G -C环闭合碱基对也是PTL形成的主要决定因素。通过将G-C闭合碱基对更改为C-G,PTL切换为六环。讨论了将这些规则与其他来源的常规三环发夹和PTL进行比较,以及在人类泡沫病毒和其他spumaretroviruses中保留PTL的情况。

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