Regular, intense exercise training as a healthy aging lifestyle strategy: preventing DNA damage, telomere shortening and adverse DNA methylation changes over a lifetime
Article
Article Title | Regular, intense exercise training as a healthy aging lifestyle strategy: preventing DNA damage, telomere shortening and adverse DNA methylation changes over a lifetime |
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ERA Journal ID | 210481 |
Article Category | Article |
Authors | Sellami, Maha (Author), Bragazzi, Nicola (Author), Prince, Mohammad Shoaib (Author), Denham, Joshua (Author) and Elrayess, Mohamed (Author) |
Journal Title | Frontiers in Genetics |
Journal Citation | 12, pp. 1-12 |
Article Number | 652497 |
Number of Pages | 12 |
Year | 2021 |
Place of Publication | Lausanne, Switzerland |
ISSN | 1664-8021 |
Digital Object Identifier (DOI) | https://doi.org/10.3389/fgene.2021.652497 |
Web Address (URL) | https://www.frontiersin.org/articles/10.3389/fgene.2021.652497/full |
Abstract | Exercise training is one of the few therapeutic interventions that improves health span by delaying the onset of age-related diseases and preventing early death. The length of telomeres, the 5 '-TTAGGG(n)-3 ' tandem repeats at the ends of mammalian chromosomes, is one of the main indicators of biological age. Telomeres undergo shortening with each cellular division. This subsequently leads to alterations in the expression of several genes that encode vital proteins with critical functions in many tissues throughout the body, and ultimately impacts cardiovascular, immune and muscle physiology. The sub-telomeric DNA is comprised of heavily methylated, heterochromatin. Methylation and histone acetylation are two of the most well-studied examples of the epigenetic modifications that occur on histone proteins. DNA methylation is the type of epigenetic modification that alters gene expression without modifying gene sequence. Although diet, genetic predisposition and a healthy lifestyle seem to alter DNA methylation and telomere length (TL), recent evidence suggests that training status or physical fitness are some of the major factors that control DNA structural modifications. In fact, TL is positively associated with cardiorespiratory fitness, physical activity level (sedentary, active, moderately trained, or elite) and training intensity, but is shorter in over-trained athletes. Similarly, somatic cells are vulnerable to exercise-induced epigenetic modification, including DNA methylation. Exercise-training load, however, depends on intensity and volume (duration and frequency). Training load-dependent responses in genomic profiles could underpin the discordant physiological and physical responses to exercise. In the current review, we will discuss the role of various forms of exercise training in the regulation of DNA damage, TL and DNA methylation status in humans, to provide an update on the influence exercise training has on biological aging. |
Keywords | physical activity, epigenetics, telomerase, gene, oxidative stress, epigenetic clock, skeletal muscle |
ANZSRC Field of Research 2020 | 310599. Genetics not elsewhere classified |
420702. Exercise physiology | |
Public Notes | Copyright © 2021 Sellami, Bragazzi, Prince, Denham and Elrayess. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
Byline Affiliations | Qatar University, Qatar |
University of Genoa, Italy | |
Royal Melbourne Institute of Technology (RMIT) | |
Institution of Origin | University of Southern Queensland |
https://research.usq.edu.au/item/q6qy6/regular-intense-exercise-training-as-a-healthy-aging-lifestyle-strategy-preventing-dna-damage-telomere-shortening-and-adverse-dna-methylation-changes-over-a-lifetime
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