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MicroRNAs miR-203-3p, miR-664-3p and miR-708-5p are associated with median strain lifespan in mice
MicroRNAs (miRNAs) are small non-coding RNA species that have been shown to have roles in multiple processes that occur in higher eukaryotes. They act by binding to specific sequences in the 3’ untranslated region of their target genes and causing the transcripts to be degraded by the RNA-induced si...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356331/ https://www.ncbi.nlm.nih.gov/pubmed/28304372 http://dx.doi.org/10.1038/srep44620 |
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author | Lee, Benjamin P. Burić, Ivana George-Pandeth, Anupriya Flurkey, Kevin Harrison, David E. Yuan, Rong Peters, Luanne L. Kuchel, George A. Melzer, David Harries, Lorna W. |
author_facet | Lee, Benjamin P. Burić, Ivana George-Pandeth, Anupriya Flurkey, Kevin Harrison, David E. Yuan, Rong Peters, Luanne L. Kuchel, George A. Melzer, David Harries, Lorna W. |
author_sort | Lee, Benjamin P. |
collection | PubMed |
description | MicroRNAs (miRNAs) are small non-coding RNA species that have been shown to have roles in multiple processes that occur in higher eukaryotes. They act by binding to specific sequences in the 3’ untranslated region of their target genes and causing the transcripts to be degraded by the RNA-induced silencing complex (RISC). MicroRNAs have previously been reported to demonstrate altered expression in several aging phenotypes such as cellular senescence and age itself. Here, we have measured the expression levels of 521 small regulatory microRNAs (miRNAs) in spleen tissue from young and old animals of 6 mouse strains with different median strain lifespans by quantitative real-time PCR. Expression levels of 3 microRNAs were robustly associated with strain lifespan, after correction for multiple statistical testing (miR-203-3p [β-coefficient = −0.6447, p = 4.8 × 10(−11)], miR-664-3p [β-coefficient = 0.5552, p = 5.1 × 10(−8)] and miR-708-5p [β-coefficient = 0.4986, p = 1.6 × 10(−6)]). Pathway analysis of binding sites for these three microRNAs revealed enrichment of target genes involved in key aging and longevity pathways including mTOR, FOXO and MAPK, most of which also demonstrated associations with longevity. Our results suggests that miR-203-3p, miR-664-3p and miR-708-5p may be implicated in pathways determining lifespan in mammals. |
format | Online Article Text |
id | pubmed-5356331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53563312017-03-22 MicroRNAs miR-203-3p, miR-664-3p and miR-708-5p are associated with median strain lifespan in mice Lee, Benjamin P. Burić, Ivana George-Pandeth, Anupriya Flurkey, Kevin Harrison, David E. Yuan, Rong Peters, Luanne L. Kuchel, George A. Melzer, David Harries, Lorna W. Sci Rep Article MicroRNAs (miRNAs) are small non-coding RNA species that have been shown to have roles in multiple processes that occur in higher eukaryotes. They act by binding to specific sequences in the 3’ untranslated region of their target genes and causing the transcripts to be degraded by the RNA-induced silencing complex (RISC). MicroRNAs have previously been reported to demonstrate altered expression in several aging phenotypes such as cellular senescence and age itself. Here, we have measured the expression levels of 521 small regulatory microRNAs (miRNAs) in spleen tissue from young and old animals of 6 mouse strains with different median strain lifespans by quantitative real-time PCR. Expression levels of 3 microRNAs were robustly associated with strain lifespan, after correction for multiple statistical testing (miR-203-3p [β-coefficient = −0.6447, p = 4.8 × 10(−11)], miR-664-3p [β-coefficient = 0.5552, p = 5.1 × 10(−8)] and miR-708-5p [β-coefficient = 0.4986, p = 1.6 × 10(−6)]). Pathway analysis of binding sites for these three microRNAs revealed enrichment of target genes involved in key aging and longevity pathways including mTOR, FOXO and MAPK, most of which also demonstrated associations with longevity. Our results suggests that miR-203-3p, miR-664-3p and miR-708-5p may be implicated in pathways determining lifespan in mammals. Nature Publishing Group 2017-03-17 /pmc/articles/PMC5356331/ /pubmed/28304372 http://dx.doi.org/10.1038/srep44620 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lee, Benjamin P. Burić, Ivana George-Pandeth, Anupriya Flurkey, Kevin Harrison, David E. Yuan, Rong Peters, Luanne L. Kuchel, George A. Melzer, David Harries, Lorna W. MicroRNAs miR-203-3p, miR-664-3p and miR-708-5p are associated with median strain lifespan in mice |
title | MicroRNAs miR-203-3p, miR-664-3p and miR-708-5p are associated with median strain lifespan in mice |
title_full | MicroRNAs miR-203-3p, miR-664-3p and miR-708-5p are associated with median strain lifespan in mice |
title_fullStr | MicroRNAs miR-203-3p, miR-664-3p and miR-708-5p are associated with median strain lifespan in mice |
title_full_unstemmed | MicroRNAs miR-203-3p, miR-664-3p and miR-708-5p are associated with median strain lifespan in mice |
title_short | MicroRNAs miR-203-3p, miR-664-3p and miR-708-5p are associated with median strain lifespan in mice |
title_sort | micrornas mir-203-3p, mir-664-3p and mir-708-5p are associated with median strain lifespan in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356331/ https://www.ncbi.nlm.nih.gov/pubmed/28304372 http://dx.doi.org/10.1038/srep44620 |
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