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MicroRNAs mir‐184 and let‐7 alter Drosophila metabolism and longevity
MicroRNAs (miRNAs) are small RNA molecules that regulate gene expression associated with many complex biological processes. By comparing miRNA expression between long‐lived cohorts of Drosophila melanogaster that were fed a low‐nutrient diet with normal‐lived control animals fed a high‐nutrient diet...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676060/ https://www.ncbi.nlm.nih.gov/pubmed/28963741 http://dx.doi.org/10.1111/acel.12673 |
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author | Gendron, Christi M. Pletcher, Scott D. |
author_facet | Gendron, Christi M. Pletcher, Scott D. |
author_sort | Gendron, Christi M. |
collection | PubMed |
description | MicroRNAs (miRNAs) are small RNA molecules that regulate gene expression associated with many complex biological processes. By comparing miRNA expression between long‐lived cohorts of Drosophila melanogaster that were fed a low‐nutrient diet with normal‐lived control animals fed a high‐nutrient diet, we identified miR‐184, let‐7, miR‐125, and miR‐100 as candidate miRNAs involved in modulating aging. We found that ubiquitous, adult‐specific overexpression of these individual miRNAs led to significant changes in fat metabolism and/or lifespan. Most impressively, adult‐specific overexpression of let‐7 in female nervous tissue increased median fly lifespan by ~22%. We provide evidence that this lifespan extension is not due to alterations in nutrient intake or to decreased insulin signaling. |
format | Online Article Text |
id | pubmed-5676060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56760602017-12-01 MicroRNAs mir‐184 and let‐7 alter Drosophila metabolism and longevity Gendron, Christi M. Pletcher, Scott D. Aging Cell Short Takes MicroRNAs (miRNAs) are small RNA molecules that regulate gene expression associated with many complex biological processes. By comparing miRNA expression between long‐lived cohorts of Drosophila melanogaster that were fed a low‐nutrient diet with normal‐lived control animals fed a high‐nutrient diet, we identified miR‐184, let‐7, miR‐125, and miR‐100 as candidate miRNAs involved in modulating aging. We found that ubiquitous, adult‐specific overexpression of these individual miRNAs led to significant changes in fat metabolism and/or lifespan. Most impressively, adult‐specific overexpression of let‐7 in female nervous tissue increased median fly lifespan by ~22%. We provide evidence that this lifespan extension is not due to alterations in nutrient intake or to decreased insulin signaling. John Wiley and Sons Inc. 2017-09-29 2017-12 /pmc/articles/PMC5676060/ /pubmed/28963741 http://dx.doi.org/10.1111/acel.12673 Text en © 2017 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Takes Gendron, Christi M. Pletcher, Scott D. MicroRNAs mir‐184 and let‐7 alter Drosophila metabolism and longevity |
title | MicroRNAs mir‐184 and let‐7 alter Drosophila metabolism and longevity |
title_full | MicroRNAs mir‐184 and let‐7 alter Drosophila metabolism and longevity |
title_fullStr | MicroRNAs mir‐184 and let‐7 alter Drosophila metabolism and longevity |
title_full_unstemmed | MicroRNAs mir‐184 and let‐7 alter Drosophila metabolism and longevity |
title_short | MicroRNAs mir‐184 and let‐7 alter Drosophila metabolism and longevity |
title_sort | micrornas mir‐184 and let‐7 alter drosophila metabolism and longevity |
topic | Short Takes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676060/ https://www.ncbi.nlm.nih.gov/pubmed/28963741 http://dx.doi.org/10.1111/acel.12673 |
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