Abstract

MicroRNAs (miRNAs) are a class of small RNA molecules that have an important regulatory role in multiple physiological and pathological processes. Their disease-specific profiles and presence in biofluids are properties that enable miRNAs to be employed as non-invasive biomarkers. In the past decades, several methods have been developed for miRNA analysis, including small RNA sequencing (RNA-seq). Small RNA-seq enables genome-wide profiling and analysis of known, as well as novel, miRNA variants. Moreover, its high sensitivity allows for profiling of low input samples such as liquid biopsies, which have now found applications in diagnostics and prognostics. Still, due to technical bias and the limited ability to capture the true miRNA representation, its potential remains unfulfilled. The introduction of many new small RNA-seq approaches that tried to minimize this bias, has led to the existence of the many small RNA-seq protocols seen today. Here, we review all current approaches to cDNA library construction used during the small RNA-seq workflow, with particular focus on their implementation in commercially available protocols. We provide an overview of each protocol and discuss their applicability. We also review recent benchmarking studies comparing each protocol’s performance and summarize the major conclusions that can be gathered from their usage. The result documents variable performance of the protocols and highlights their different applications in miRNA research. Taken together, our review provides a comprehensive overview of all the current small RNA-seq approaches, summarizes their strengths and weaknesses, and provides guidelines for their applications in miRNA research.

Highlights

  • MicroRNAs represent a class of short (~22 nucleotides) non-coding RNA molecules that are well conserved across various species

  • One strand of miRNA duplex is loaded into the Argonaut (AGO) protein, creating the RNA-induced silencing complex (RISC), which binds to the mRNA using the complementary seed sequence of the loaded mature miRNA [7]

  • We reviewed the current state of small RNA sequencing (RNA-seq) technology for analysis of miRNAs

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Summary

Introduction

MicroRNAs (miRNAs) represent a class of short (~22 nucleotides) non-coding RNA molecules that are well conserved across various species. Microarray analysis represented the most commonly used high-throughput technology for miRNA profiling [12] This hybridization-based technique does not allow for absolute quantification, identification of novel miRNAs, and separate detection of canonical miRNAs and their isomiRs, of which the importance has only started to be recognized recently [17,18,19]. Microarray-based methods usually require high quantities of input RNA This may be a limiting factor for the non-invasive analysis of liquid biopsies, where the concentration of miRNAs is rather low [20]. The disadvantages are represented by the complex experimental workflow which introduces various types of biases and demanding computational analysis To minimize these disadvantages, there have been substantial technological developments within the past five years resulting in the introduction of several new small RNA-seq protocols (Table 1). [24] [25] not available not available not available not available not available not available not available not available [26]

Small RNA-seq Technology Overview
Two-Adaptor Ligation-Based Methods
Improved Two-Adaptor Ligation-Based Methods
Ligation Free Methods
Benchmarking Studies
Conclusion
Findings
Conclusions
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