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Retrotransposons Down- and Up-Regulation in Aging Somatic Tissues
The transposon theory of aging hypothesizes the activation of transposable elements (TEs) in somatic tissues with age, leading to a shortening of the lifespan. It is thought that TE activation in aging produces an increase in DNA double-strand breaks, contributing to genome instability and promoting...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750722/ https://www.ncbi.nlm.nih.gov/pubmed/35011640 http://dx.doi.org/10.3390/cells11010079 |
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author | Giordani, Giorgia Cavaliere, Valeria Gargiulo, Giuseppe Lattanzi, Giovanna Andrenacci, Davide |
author_facet | Giordani, Giorgia Cavaliere, Valeria Gargiulo, Giuseppe Lattanzi, Giovanna Andrenacci, Davide |
author_sort | Giordani, Giorgia |
collection | PubMed |
description | The transposon theory of aging hypothesizes the activation of transposable elements (TEs) in somatic tissues with age, leading to a shortening of the lifespan. It is thought that TE activation in aging produces an increase in DNA double-strand breaks, contributing to genome instability and promoting the activation of inflammatory responses. To investigate how TE regulation changes in somatic tissues during aging, we analyzed the expression of some TEs, as well as a source of small RNAs that specifically silence the analyzed TEs; the Drosophila cluster named flamenco. We found significant variations in the expression levels of all the analyzed TEs during aging, with a trend toward reduction in middle-aged adults and reactivation in older individuals that suggests dynamic regulation during the lifespan. |
format | Online Article Text |
id | pubmed-8750722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87507222022-01-12 Retrotransposons Down- and Up-Regulation in Aging Somatic Tissues Giordani, Giorgia Cavaliere, Valeria Gargiulo, Giuseppe Lattanzi, Giovanna Andrenacci, Davide Cells Communication The transposon theory of aging hypothesizes the activation of transposable elements (TEs) in somatic tissues with age, leading to a shortening of the lifespan. It is thought that TE activation in aging produces an increase in DNA double-strand breaks, contributing to genome instability and promoting the activation of inflammatory responses. To investigate how TE regulation changes in somatic tissues during aging, we analyzed the expression of some TEs, as well as a source of small RNAs that specifically silence the analyzed TEs; the Drosophila cluster named flamenco. We found significant variations in the expression levels of all the analyzed TEs during aging, with a trend toward reduction in middle-aged adults and reactivation in older individuals that suggests dynamic regulation during the lifespan. MDPI 2021-12-28 /pmc/articles/PMC8750722/ /pubmed/35011640 http://dx.doi.org/10.3390/cells11010079 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Giordani, Giorgia Cavaliere, Valeria Gargiulo, Giuseppe Lattanzi, Giovanna Andrenacci, Davide Retrotransposons Down- and Up-Regulation in Aging Somatic Tissues |
title | Retrotransposons Down- and Up-Regulation in Aging Somatic Tissues |
title_full | Retrotransposons Down- and Up-Regulation in Aging Somatic Tissues |
title_fullStr | Retrotransposons Down- and Up-Regulation in Aging Somatic Tissues |
title_full_unstemmed | Retrotransposons Down- and Up-Regulation in Aging Somatic Tissues |
title_short | Retrotransposons Down- and Up-Regulation in Aging Somatic Tissues |
title_sort | retrotransposons down- and up-regulation in aging somatic tissues |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750722/ https://www.ncbi.nlm.nih.gov/pubmed/35011640 http://dx.doi.org/10.3390/cells11010079 |
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