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RNA结合蛋白表征方面的进展。

Advances in the characterization of RNA-binding proteins.

作者信息

Marchese Domenica, de Groot Natalia Sanchez, Lorenzo Gotor Nieves, Livi Carmen Maria, Tartaglia Gian G

机构信息

Centre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.

Universitat Pompeu Fabra (UPF), Barcelona, Spain.

出版信息

Wiley Interdiscip Rev RNA. 2016 Nov;7(6):793-810. doi: 10.1002/wrna.1378. Epub 2016 Aug 8.

DOI:10.1002/wrna.1378
PMID:27503141
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5113702/
Abstract

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 For further resources related to this article, please visit the WIREs website.

摘要

从转录到运输、储存和翻译,RNA都依赖于与不同的RNA结合蛋白(RBP)相互作用。基于新一代测序和蛋白质质谱分析的方法已开始揭示RBP在全基因组范围内的相互作用,但许多方面仍不为人所知。在高通量筛选中鉴定出的结合位点有多少是有功能的?人们已开发出多种计算方法来分析实验数据,并深入了解蛋白质与RNA相互作用的特异性。如何利用理论模型来鉴定RBP?除了寡聚复合物外,蛋白质和RNA分子还能形成颗粒状聚集体,但其物理性质仍知之甚少。哪些蛋白质特征促进颗粒形成,这些聚集体对细胞功能有何影响?在这里,我们描述了蛋白质与RNA相互作用领域最新的计算机模拟、体外和体内研究进展。我们还提出了实验和计算方法在未来研究中将要面临的挑战。《WIREs RNA》2016年,7卷:793 - 810页。doi: 10.1002/wrna.1378 有关本文的更多资源,请访问WIREs网站。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a946/5113702/3c4714cd4fa7/WRNA-7-793-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a946/5113702/99155a2c352f/WRNA-7-793-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a946/5113702/5d5154e98b77/WRNA-7-793-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a946/5113702/dddc5c0eaac8/WRNA-7-793-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a946/5113702/3c4714cd4fa7/WRNA-7-793-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a946/5113702/99155a2c352f/WRNA-7-793-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a946/5113702/5d5154e98b77/WRNA-7-793-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a946/5113702/dddc5c0eaac8/WRNA-7-793-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a946/5113702/3c4714cd4fa7/WRNA-7-793-g005.jpg

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