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The mitochondrial genome, paternal age and telomere length in humans

Telomere length (TL) in humans is highly heritable and undergoes progressive age-dependent shortening in somatic cells. By contrast, sperm donated by older men display comparatively long telomeres, presumably because in the male germline, telomeres become longer with age. This puzzling phenomenon mi...

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Detalles Bibliográficos
Autor principal: Aviv, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784075/
https://www.ncbi.nlm.nih.gov/pubmed/29335382
http://dx.doi.org/10.1098/rstb.2017.0210
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author Aviv, Abraham
author_facet Aviv, Abraham
author_sort Aviv, Abraham
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description Telomere length (TL) in humans is highly heritable and undergoes progressive age-dependent shortening in somatic cells. By contrast, sperm donated by older men display comparatively long telomeres, presumably because in the male germline, telomeres become longer with age. This puzzling phenomenon might explain why TL in the offspring correlates positively with paternal age. The present communication proposes that mitochondrial DNA polymorphisms and heteroplasmy cause variation in the production of reactive oxygen species, which, in turn, mediate age-dependent selection of germ stem cells with long telomeres and hence sperm with long telomeres. These long telomeres are then inherited by the offspring. The effect of paternal age on the offspring TL might be an evolutionarily driven mechanism that helps regulate TL across the human population. This article is part of the theme issue ‘Understanding diversity in telomere dynamics’.
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spelling pubmed-57840752018-01-30 The mitochondrial genome, paternal age and telomere length in humans Aviv, Abraham Philos Trans R Soc Lond B Biol Sci Articles Telomere length (TL) in humans is highly heritable and undergoes progressive age-dependent shortening in somatic cells. By contrast, sperm donated by older men display comparatively long telomeres, presumably because in the male germline, telomeres become longer with age. This puzzling phenomenon might explain why TL in the offspring correlates positively with paternal age. The present communication proposes that mitochondrial DNA polymorphisms and heteroplasmy cause variation in the production of reactive oxygen species, which, in turn, mediate age-dependent selection of germ stem cells with long telomeres and hence sperm with long telomeres. These long telomeres are then inherited by the offspring. The effect of paternal age on the offspring TL might be an evolutionarily driven mechanism that helps regulate TL across the human population. This article is part of the theme issue ‘Understanding diversity in telomere dynamics’. The Royal Society 2018-03-05 2018-01-15 /pmc/articles/PMC5784075/ /pubmed/29335382 http://dx.doi.org/10.1098/rstb.2017.0210 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Aviv, Abraham
The mitochondrial genome, paternal age and telomere length in humans
title The mitochondrial genome, paternal age and telomere length in humans
title_full The mitochondrial genome, paternal age and telomere length in humans
title_fullStr The mitochondrial genome, paternal age and telomere length in humans
title_full_unstemmed The mitochondrial genome, paternal age and telomere length in humans
title_short The mitochondrial genome, paternal age and telomere length in humans
title_sort mitochondrial genome, paternal age and telomere length in humans
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784075/
https://www.ncbi.nlm.nih.gov/pubmed/29335382
http://dx.doi.org/10.1098/rstb.2017.0210
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