Method Article

Circulating MicroRNA Quantification Using DNA-binding Dye Chemistry and Droplet Digital PCR

DOI:

10.3791/54102

June 26th, 2016

In This Article

Summary

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A sensitive and accurate method for cell-free microRNAs quantification using a dye-based chemistry and droplet digital PCR technology is described.

Abstract

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Circulating (of cell-free) microRNAs (miRNAs) are released from cells into the blood stream. The amount of specific microRNAs in the circulation has been linked to a disease state and has the potential to be used as disease biomarker. A sensitive and accurate method for circulating microRNA quantification using a dye-based chemistry and droplet digital PCR technology has been recently developed. Specifically, using Locked Nucleic Acid (LNA)-based miRNA-specific primers with a green fluorescent DNA-binding dye in a compatible droplet digital PCR system it is possible to obtain the absolute quantification of specific miRNAs. Here, we describe how performing this technique to assess miRNA amount in biological fluids, such as plasma and serum, is both feasible and effective.

Introduction

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MicroRNAs (miRNAs) are released into blood circulation by potentially all the cells of the organism, as a consequence of active release or necrotic and apoptotic processes. Cell-free miRNAs have been detected in the bloodstream either as free stable molecules or linked to lipoproteins or enveloped inside exosomes and microvesicles 1-3. They are believed to function as cell-to-cell communicators 4, and their amount changes in the presence of cancer, cardiac disorders or autoimmune diseases 5-7. Their accurate and reproducible quantification is the basis for their evaluation as disease biomarkers. However, for several reasons already des....

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Protocol

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MicroRNA Isolation from Plasma or Serum

Note: Plasma and serum preparation is a relevant step in circulating miRNA quantification. There is no preferred procedure for plasma and serum preparation. The only important thing to consider is that all the samples from the same experiment must be processed using exactly the same workflow. Start from 200 µl serum or plasma. Total RNA can be isolated from serum or plasma using commercially available kits.

1. Protocol for Total RNA (including miRNA) Isolation

  1. Thaw serum/plasma samples on ice.
  2. Add 1 ml of Lysis Reagent (e.g., QIAzol) to 200 µl serum/plasma....

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Results

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The absolute amount of specific miRNAs per ml of plasma or serum can be determined using a green fluorescent DNA-binding dye and droplet digital PCR technology. Figure 1 presents the process of positive-droplets selection, which determines the final miRNA concentration (copies/µl) in the amplification reaction calculated by the analysis software. The amount of each miRNA in the blood is very different, being some miRNA species more abundant than others. Using a 1:50 dilut.......

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Discussion

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Circulating miRNAs are present in blood at extremely low concentrations and the amount of RNA that can be extracted from plasma and serum samples is low. For this reason, they are difficult to quantify with other techniques such as microarray and RNA sequencing. Moreover, there is a generalized lack of agreement on data normalization and the presence of endogenous "reference" miRNAs in the blood. In this context, a sensitive technology like droplet digital PCR, capable of counting the number of miRNA copies per m.......

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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Supported by funding from the Italian Association for Cancer Research (AIRC) to MF (MFAG 11676) and to MN (Special Program Molecular Clinical Oncology - 5 per mille n. 9980, 2010/15) and from the Italian Ministry of Instruction, University and Research FIRB 2011 to MN (Project RBAPIIBYNP).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
miRNeasy Mini KitQiagen217004Columns for total RNA, including miRNA, extraction from serum/plasma
100 nmole RNA oligo Cel-miR-39-3pIntegrated DNA TechnologiesCustomSequence: UCACCGGGUGUAAAUCAGCUUG
Universal cDNA synthesis kit II, 8-64 rxnsExiqon203301Kit for microRNA reverse transcription
MicroRNA LNA PCR primer set Exiqon204000-206xxx and 2100000-21xxxxxPrimers for miRNA amplification inside droplets
QX200 droplet generatorBioRad186-4002Instrument used for droplet reading
QX200 droplet readerBioRad186-4003Instrument used for droplet generation
QuantaSoft softwareBioRad186-3007Software for data collection and analysis
PX1 PCR plate sealerBioRad181-4000Plate sealer
DG8 droplet generator cartridges and gasketsBioRad186-4008Cartridges used to mix sample and oil to generate droplets
QX200 ddPCR EvaGreen supermixBioRad186-4033/36PCR supermix
QX200 droplet generator oil for EvaGreen dyeBioRad186-4005Oil for droplet generation

References

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  1. Arroyo, J. D., et al. Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma. Proc Natl Acad Sci U S A. 108, 5003-5008 (2011).
  2. Skog, J., et al.

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Tags

Circulating MicroRNADroplet Digital PCRDNA binding DyeLNA based PrimersAbsolute QuantificationPlasma Serum AnalysisEvaGreen Master MixDroplet GenerationThermal CyclingQuantaLife Software

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