核糖核酸
计算生物学
生物信息学
RNA结合蛋白
生物
化学
核糖开关
细胞生物学
非编码RNA
生物化学
核酸
遗传学
基因
作者
Domenica Marchese,Natalia Sánchez de Groot,Nieves Lorenzo Gotor,Carmen Maria Livi,Gian Gaetano Tartaglia
摘要
From transcription, to transport, storage, and translation, RNA depends on association with different RNA ‐binding proteins ( RBPs ). Methods based on next‐generation sequencing and protein mass‐spectrometry have started to unveil genome‐wide interactions of RBPs but many aspects still remain out of sight. How many of the binding sites identified in high‐throughput screenings are functional? A number of computational methods have been developed to analyze experimental data and to obtain insights into the specificity of protein– RNA interactions. How can theoretical models be exploited to identify RBPs ? In addition to oligomeric complexes, protein and RNA molecules can associate into granular assemblies whose physical properties are still poorly understood. What protein features promote granule formation and what effects do these assemblies have on cell function? Here, we describe the newest in silico , in vitro , and in vivo advances in the field of protein– RNA interactions. We also present the challenges that experimental and computational approaches will have to face in future studies. WIREs RNA 2016, 7:793–810. doi: 10.1002/wrna.1378 This article is categorized under: RNA Interactions with Proteins and Other Molecules > Protein–RNA Recognition RNA Interactions with Proteins and Other Molecules > RNA–Protein Complexes RNA in Disease and Development > RNA in Disease
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