Abstract
The interaction between non-coding RNAs (ncRNAs) and proteins is crucial for the stability, localization and function of the different classes of ncRNAs. Although ncRNAs, when embedded in various ribonucleoprotein (RNP) complexes, control the fundamental processes of gene expression, their biological functions and mechanisms of action are still largely unexplored. Mass Spectrometry (MS)-based proteomics has emerged as powerful tool to study the ncRNA world: on the one hand, by identifying the proteins interacting with distinct ncRNAs; on the other hand, by measuring the impact of ncRNAs on global protein levels. Here, we will first provide a concise overview on the basic principles of MS-based proteomics for systematic protein identification and quantification; then, we will recapitulate the main approaches that have been implemented for the screening of ncRNA interactors and the dissection of ncRNA-protein complex composition. Finally, we will describe examples of various proteomics strategies developed to characterize the effect of ncRNAs on gene expression, with a focus on the systematic identification of microRNA (miRNA) targets.
Highlights
Non-coding RNAs are generally defined as transcribed, but not translated RNAs
The in-depth analysis of the mammalian transcriptome by High Throughput Sequencing (HTS) technologies revealed the existence of different types of ncRNAs including: transfer RNAs (tRNAs), ribosomal RNAs (rRNAs), small nucleolar RNAs, microRNAs, long non-coding RNAs, circular RNAs, pseudogenes, and piwiRNAs
Different classes of ncRNAs, including miRNAs and long non-coding RNAs (lncRNAs), have been described as key regulators of gene expression; with the increasing knowledge gained through HTS, novel and less characterized classes of ncRNAs will be probably included in the same regulatory group, as was the case for the recently reported circRNAs (Huang et al, 2017)
Summary
Non-coding RNAs (ncRNAs) are generally defined as transcribed, but not translated RNAs.
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