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Robust profiling of microRNAs and isomiRs in human plasma exosomes across 46 individuals
microRNAs (miRNAs) are small double stranded RNA molecules consisting of two complementary strands called the 5p and 3p arms. Following imprecise processing and/or addition of nucleotides at the ends, miRNA biogenesis can give rise to variants called isomiRs. Exosomes are small vesicles released by...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934752/ https://www.ncbi.nlm.nih.gov/pubmed/31882820 http://dx.doi.org/10.1038/s41598-019-56593-7 |
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author | Karlsen, Tommy A. Aae, Tommy F. Brinchmann, Jan E. |
author_facet | Karlsen, Tommy A. Aae, Tommy F. Brinchmann, Jan E. |
author_sort | Karlsen, Tommy A. |
collection | PubMed |
description | microRNAs (miRNAs) are small double stranded RNA molecules consisting of two complementary strands called the 5p and 3p arms. Following imprecise processing and/or addition of nucleotides at the ends, miRNA biogenesis can give rise to variants called isomiRs. Exosomes are small vesicles released by cells. They have attracted attention due to their potential use in biomarker development because of their content of biomolecules, including miRNAs and isomiRs. Exosomes are found in body fluids such as plasma. In this study we used next generation sequencing to investigate the distribution of 5p and 3p arms of both miRNAs and isomiRs in plasma exosomes from 46 individuals. Among the canonical miRNAs there was similar prevalence between 5p and 3p miRNAs. Most of the miRNAs had isomiRs, and in approximately half of the cases an isomiR was more abundant than the corresponding canonical miRNA. Most of the isomiRs were generated from 5p miRNAs. There were very small differences in the concentration of canonical miRNA and isomiR sequences between donors, suggesting tight control of isomiR generation and sorting into exosomes. IsomiRs are abundant in plasma exosomes and should be included in analysis when plasma exosomal miRNAs are investigated as potential biomarkers for disease development. |
format | Online Article Text |
id | pubmed-6934752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69347522019-12-31 Robust profiling of microRNAs and isomiRs in human plasma exosomes across 46 individuals Karlsen, Tommy A. Aae, Tommy F. Brinchmann, Jan E. Sci Rep Article microRNAs (miRNAs) are small double stranded RNA molecules consisting of two complementary strands called the 5p and 3p arms. Following imprecise processing and/or addition of nucleotides at the ends, miRNA biogenesis can give rise to variants called isomiRs. Exosomes are small vesicles released by cells. They have attracted attention due to their potential use in biomarker development because of their content of biomolecules, including miRNAs and isomiRs. Exosomes are found in body fluids such as plasma. In this study we used next generation sequencing to investigate the distribution of 5p and 3p arms of both miRNAs and isomiRs in plasma exosomes from 46 individuals. Among the canonical miRNAs there was similar prevalence between 5p and 3p miRNAs. Most of the miRNAs had isomiRs, and in approximately half of the cases an isomiR was more abundant than the corresponding canonical miRNA. Most of the isomiRs were generated from 5p miRNAs. There were very small differences in the concentration of canonical miRNA and isomiR sequences between donors, suggesting tight control of isomiR generation and sorting into exosomes. IsomiRs are abundant in plasma exosomes and should be included in analysis when plasma exosomal miRNAs are investigated as potential biomarkers for disease development. Nature Publishing Group UK 2019-12-27 /pmc/articles/PMC6934752/ /pubmed/31882820 http://dx.doi.org/10.1038/s41598-019-56593-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Karlsen, Tommy A. Aae, Tommy F. Brinchmann, Jan E. Robust profiling of microRNAs and isomiRs in human plasma exosomes across 46 individuals |
title | Robust profiling of microRNAs and isomiRs in human plasma exosomes across 46 individuals |
title_full | Robust profiling of microRNAs and isomiRs in human plasma exosomes across 46 individuals |
title_fullStr | Robust profiling of microRNAs and isomiRs in human plasma exosomes across 46 individuals |
title_full_unstemmed | Robust profiling of microRNAs and isomiRs in human plasma exosomes across 46 individuals |
title_short | Robust profiling of microRNAs and isomiRs in human plasma exosomes across 46 individuals |
title_sort | robust profiling of micrornas and isomirs in human plasma exosomes across 46 individuals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6934752/ https://www.ncbi.nlm.nih.gov/pubmed/31882820 http://dx.doi.org/10.1038/s41598-019-56593-7 |
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