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Nuclear respiratory factor 1 and endurance exercise promote human telomere transcription

DNA breaks activate the DNA damage response and, if left unrepaired, trigger cellular senescence. Telomeres are specialized nucleoprotein structures that protect chromosome ends from persistent DNA damage response activation. Whether protection can be enhanced to counteract the age-dependent decline...

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Autores principales: Diman, Aurélie, Boros, Joanna, Poulain, Florian, Rodriguez, Julie, Purnelle, Marin, Episkopou, Harikleia, Bertrand, Luc, Francaux, Marc, Deldicque, Louise, Decottignies, Anabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087959/
https://www.ncbi.nlm.nih.gov/pubmed/27819056
http://dx.doi.org/10.1126/sciadv.1600031
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author Diman, Aurélie
Boros, Joanna
Poulain, Florian
Rodriguez, Julie
Purnelle, Marin
Episkopou, Harikleia
Bertrand, Luc
Francaux, Marc
Deldicque, Louise
Decottignies, Anabelle
author_facet Diman, Aurélie
Boros, Joanna
Poulain, Florian
Rodriguez, Julie
Purnelle, Marin
Episkopou, Harikleia
Bertrand, Luc
Francaux, Marc
Deldicque, Louise
Decottignies, Anabelle
author_sort Diman, Aurélie
collection PubMed
description DNA breaks activate the DNA damage response and, if left unrepaired, trigger cellular senescence. Telomeres are specialized nucleoprotein structures that protect chromosome ends from persistent DNA damage response activation. Whether protection can be enhanced to counteract the age-dependent decline in telomere integrity is a challenging question. Telomeric repeat–containing RNA (TERRA), which is transcribed from telomeres, emerged as important player in telomere integrity. However, how human telomere transcription is regulated is still largely unknown. We identify nuclear respiratory factor 1 and peroxisome proliferator–activated receptor γ coactivator 1α as regulators of human telomere transcription. In agreement with an upstream regulation of these factors by adenosine 5′-monophosphate (AMP)–activated protein kinase (AMPK), pharmacological activation of AMPK in cancer cell lines or in normal nonproliferating myotubes up-regulated TERRA, thereby linking metabolism to telomere fitness. Cycling endurance exercise, which is associated with AMPK activation, increased TERRA levels in skeletal muscle biopsies obtained from 10 healthy young volunteers. The data support the idea that exercise may protect against aging.
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spelling pubmed-50879592016-11-04 Nuclear respiratory factor 1 and endurance exercise promote human telomere transcription Diman, Aurélie Boros, Joanna Poulain, Florian Rodriguez, Julie Purnelle, Marin Episkopou, Harikleia Bertrand, Luc Francaux, Marc Deldicque, Louise Decottignies, Anabelle Sci Adv Research Articles DNA breaks activate the DNA damage response and, if left unrepaired, trigger cellular senescence. Telomeres are specialized nucleoprotein structures that protect chromosome ends from persistent DNA damage response activation. Whether protection can be enhanced to counteract the age-dependent decline in telomere integrity is a challenging question. Telomeric repeat–containing RNA (TERRA), which is transcribed from telomeres, emerged as important player in telomere integrity. However, how human telomere transcription is regulated is still largely unknown. We identify nuclear respiratory factor 1 and peroxisome proliferator–activated receptor γ coactivator 1α as regulators of human telomere transcription. In agreement with an upstream regulation of these factors by adenosine 5′-monophosphate (AMP)–activated protein kinase (AMPK), pharmacological activation of AMPK in cancer cell lines or in normal nonproliferating myotubes up-regulated TERRA, thereby linking metabolism to telomere fitness. Cycling endurance exercise, which is associated with AMPK activation, increased TERRA levels in skeletal muscle biopsies obtained from 10 healthy young volunteers. The data support the idea that exercise may protect against aging. American Association for the Advancement of Science 2016-07-27 /pmc/articles/PMC5087959/ /pubmed/27819056 http://dx.doi.org/10.1126/sciadv.1600031 Text en Copyright © 2016, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Diman, Aurélie
Boros, Joanna
Poulain, Florian
Rodriguez, Julie
Purnelle, Marin
Episkopou, Harikleia
Bertrand, Luc
Francaux, Marc
Deldicque, Louise
Decottignies, Anabelle
Nuclear respiratory factor 1 and endurance exercise promote human telomere transcription
title Nuclear respiratory factor 1 and endurance exercise promote human telomere transcription
title_full Nuclear respiratory factor 1 and endurance exercise promote human telomere transcription
title_fullStr Nuclear respiratory factor 1 and endurance exercise promote human telomere transcription
title_full_unstemmed Nuclear respiratory factor 1 and endurance exercise promote human telomere transcription
title_short Nuclear respiratory factor 1 and endurance exercise promote human telomere transcription
title_sort nuclear respiratory factor 1 and endurance exercise promote human telomere transcription
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087959/
https://www.ncbi.nlm.nih.gov/pubmed/27819056
http://dx.doi.org/10.1126/sciadv.1600031
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