Current Technical Approaches to Study RNA–Protein Interactions in mRNAs and Long Non-Coding RNAs

BioChem Pub Date : 2022-12-30 DOI:10.3390/biochem3010001
Johanna Mattay
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Abstract

It is commonly understood that RNA-binding proteins crucially determine the fate of their target RNAs. Vice versa, RNAs are becoming increasingly recognized for their functions in protein regulation and the dynamics of RNA-protein complexes. Long non-coding RNAs are emerging as potent regulators of proteins that exert unknown RNA-binding properties and moonlighting functions. A vast array of RNA- and protein-centric techniques have been developed for the identification of protein and RNA targets, respectively, including unbiased protein mass spectrometry and next-generation RNA sequencing as readout. Determining true physiological RNA and protein targets is challenging as RNA–protein interaction is highly dynamic, tissue- and cell-type-specific, and changes with the environment. Here I review current techniques for the analysis of RNA–protein interactions in living cells and in vitro. RNA-centric techniques are presented on the basis of cross-linking or the use of alternative approaches. Protein-centric approaches are discussed in combination with high-throughput sequencing. Finally, the impact of mutations in RNA–protein complexes on human disease is highlighted.
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研究mrna和长链非编码rna中rna -蛋白相互作用的当前技术方法
人们普遍认为,rna结合蛋白至关重要地决定了其靶rna的命运。反之亦然,rna在蛋白质调控和rna -蛋白质复合物动力学方面的功能越来越得到认可。长链非编码rna正在成为发挥未知rna结合特性和兼职功能的蛋白质的有效调节因子。大量以RNA和蛋白质为中心的技术已经被开发出来,分别用于鉴定蛋白质和RNA靶标,包括无偏蛋白质质谱法和下一代RNA测序作为读数。确定真正的生理RNA和蛋白质靶标是具有挑战性的,因为RNA -蛋白质相互作用是高度动态的,具有组织和细胞类型特异性,并随环境而变化。在这里,我回顾了目前在活细胞和体外分析rna -蛋白相互作用的技术。以rna为中心的技术是在交联或使用替代方法的基础上提出的。以蛋白质为中心的方法与高通量测序相结合进行了讨论。最后,强调了rna -蛋白复合物突变对人类疾病的影响。
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