» Articles » PMID: 37511412

Phospho-RNA-Seq Highlights Specific Small RNA Profiles in Plasma Extracellular Vesicles

Abstract

Small RNAs (sRNAs) are bioactive molecules that can be detected in biofluids, reflecting physiological and pathological states. In plasma, sRNAs are found within extracellular vesicles (EVs) and in extravesicular compartments, offering potential sources of highly sensitive biomarkers. Deep sequencing strategies to profile sRNAs favor the detection of microRNAs (miRNAs), the best-known class of sRNAs. Phospho-RNA-seq, through the enzymatic treatment of sRNAs with T4 polynucleotide kinase (T4-PNK), has been recently developed to increase the detection of thousands of previously inaccessible RNAs. In this study, we investigated the value of phospho-RNA-seq on both the EVs and extravesicular plasma subfractions. Phospho-RNA-seq increased the proportion of sRNAs used for alignment and highlighted the diversity of the sRNA transcriptome. Unsupervised clustering analysis using sRNA counts matrices correctly classified the EVs and extravesicular samples only in the T4-PNK treated samples, indicating that phospho-RNA-seq stresses the features of sRNAs in each plasma subfraction. Furthermore, T4-PNK treatment emphasized specific miRNA variants differing in the 5'-end (5'-isomiRs) and certain types of tRNA fragments in each plasma fraction. Phospho-RNA-seq increased the number of tissue-specific messenger RNA (mRNA) fragments in the EVs compared with the extravesicular fraction, suggesting that phospho-RNA-seq favors the discovery of tissue-specific sRNAs in EVs. Overall, the present data emphasizes the value of phospho-RNA-seq in uncovering RNA-based biomarkers in EVs.

Citing Articles

Methodological Assessment of ExoGAG for Isolation of Cerebrospinal Fluid Extracellular Vesicles as a Source of Biomarkers.

Salvat-Rovira N, Vazquez-Oliver A, Rivas-Asensio E, Herrero-Lorenzo M, Gamez-Valero A, Perez-Perez J Int J Mol Sci. 2025; 25(24.

PMID: 39769471 PMC: 11679985. DOI: 10.3390/ijms252413705.


A Comprehensive Review on Circulating cfRNA in Plasma: Implications for Disease Diagnosis and Beyond.

Zhong P, Bai L, Hong M, Ouyang J, Wang R, Zhang X Diagnostics (Basel). 2024; 14(10).

PMID: 38786343 PMC: 11119755. DOI: 10.3390/diagnostics14101045.


Challenges in characterization of transcriptomes of extracellular vesicles and non-vesicular extracellular RNA carriers.

Makarova J, Maltseva D, Tonevitsky A Front Mol Biosci. 2023; 10:1327985.

PMID: 38116380 PMC: 10729812. DOI: 10.3389/fmolb.2023.1327985.

References
1.
Kozomara A, Birgaoanu M, Griffiths-Jones S . miRBase: from microRNA sequences to function. Nucleic Acids Res. 2018; 47(D1):D155-D162. PMC: 6323917. DOI: 10.1093/nar/gky1141. View

2.
Murillo O, Thistlethwaite W, Rozowsky J, Subramanian S, Lucero R, Shah N . exRNA Atlas Analysis Reveals Distinct Extracellular RNA Cargo Types and Their Carriers Present across Human Biofluids. Cell. 2019; 177(2):463-477.e15. PMC: 6616370. DOI: 10.1016/j.cell.2019.02.018. View

3.
Fritz J, Heintz-Buschart A, Ghosal A, Wampach L, Etheridge A, Galas D . Sources and Functions of Extracellular Small RNAs in Human Circulation. Annu Rev Nutr. 2016; 36:301-36. PMC: 5479634. DOI: 10.1146/annurev-nutr-071715-050711. View

4.
Monguio-Tortajada M, Roura S, Galvez-Monton C, Pujal J, Aran G, Sanjurjo L . Nanosized UCMSC-derived extracellular vesicles but not conditioned medium exclusively inhibit the inflammatory response of stimulated T cells: implications for nanomedicine. Theranostics. 2017; 7(2):270-284. PMC: 5197063. DOI: 10.7150/thno.16154. View

5.
Mizenko R, Brostoff T, Rojalin T, Koster H, Swindell H, Leiserowitz G . Tetraspanins are unevenly distributed across single extracellular vesicles and bias sensitivity to multiplexed cancer biomarkers. J Nanobiotechnology. 2021; 19(1):250. PMC: 8379740. DOI: 10.1186/s12951-021-00987-1. View