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Fungal Ku prevents permanent cell cycle arrest by suppressing DNA damage signaling at telomeres

The Ku heterodimer serves in the initial step in repairing DNA double-strand breaks by the non-homologous end-joining pathway. Besides this key function, Ku also plays a role in other cellular processes including telomere maintenance. Inactivation of Ku can lead to DNA repair defects and telomere ab...

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Autores principales: de Sena-Tomás, Carmen, Yu, Eun Young, Calzada, Arturo, Holloman, William K., Lue, Neal F., Pérez-Martín, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4344518/
https://www.ncbi.nlm.nih.gov/pubmed/25653166
http://dx.doi.org/10.1093/nar/gkv082
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author de Sena-Tomás, Carmen
Yu, Eun Young
Calzada, Arturo
Holloman, William K.
Lue, Neal F.
Pérez-Martín, José
author_facet de Sena-Tomás, Carmen
Yu, Eun Young
Calzada, Arturo
Holloman, William K.
Lue, Neal F.
Pérez-Martín, José
author_sort de Sena-Tomás, Carmen
collection PubMed
description The Ku heterodimer serves in the initial step in repairing DNA double-strand breaks by the non-homologous end-joining pathway. Besides this key function, Ku also plays a role in other cellular processes including telomere maintenance. Inactivation of Ku can lead to DNA repair defects and telomere aberrations. In model organisms where Ku has been studied, inactivation can lead to DNA repair defects and telomere aberrations. In general Ku deficient mutants are viable, but a notable exception to this is human where Ku has been found to be essential. Here we report that similar to the situation in human Ku is required for cell proliferation in the fungus Ustilago maydis. Using conditional strains for Ku expression, we found that cells arrest permanently in G2 phase when Ku expression is turned off. Arrest results from cell cycle checkpoint activation due to persistent signaling via the DNA damage response (DDR). Our results point to the telomeres as the most likely source of the DNA damage signal. Inactivation of the DDR makes the Ku complex dispensable for proliferation in this organism. Our findings suggest that in U. maydis, unprotected telomeres arising from Ku depletion are the source of the signal that activates the DDR leading to cell cycle arrest.
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spelling pubmed-43445182015-03-17 Fungal Ku prevents permanent cell cycle arrest by suppressing DNA damage signaling at telomeres de Sena-Tomás, Carmen Yu, Eun Young Calzada, Arturo Holloman, William K. Lue, Neal F. Pérez-Martín, José Nucleic Acids Res Genome Integrity, Repair and Replication The Ku heterodimer serves in the initial step in repairing DNA double-strand breaks by the non-homologous end-joining pathway. Besides this key function, Ku also plays a role in other cellular processes including telomere maintenance. Inactivation of Ku can lead to DNA repair defects and telomere aberrations. In model organisms where Ku has been studied, inactivation can lead to DNA repair defects and telomere aberrations. In general Ku deficient mutants are viable, but a notable exception to this is human where Ku has been found to be essential. Here we report that similar to the situation in human Ku is required for cell proliferation in the fungus Ustilago maydis. Using conditional strains for Ku expression, we found that cells arrest permanently in G2 phase when Ku expression is turned off. Arrest results from cell cycle checkpoint activation due to persistent signaling via the DNA damage response (DDR). Our results point to the telomeres as the most likely source of the DNA damage signal. Inactivation of the DDR makes the Ku complex dispensable for proliferation in this organism. Our findings suggest that in U. maydis, unprotected telomeres arising from Ku depletion are the source of the signal that activates the DDR leading to cell cycle arrest. Oxford University Press 2015-02-27 2015-02-04 /pmc/articles/PMC4344518/ /pubmed/25653166 http://dx.doi.org/10.1093/nar/gkv082 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Genome Integrity, Repair and Replication
de Sena-Tomás, Carmen
Yu, Eun Young
Calzada, Arturo
Holloman, William K.
Lue, Neal F.
Pérez-Martín, José
Fungal Ku prevents permanent cell cycle arrest by suppressing DNA damage signaling at telomeres
title Fungal Ku prevents permanent cell cycle arrest by suppressing DNA damage signaling at telomeres
title_full Fungal Ku prevents permanent cell cycle arrest by suppressing DNA damage signaling at telomeres
title_fullStr Fungal Ku prevents permanent cell cycle arrest by suppressing DNA damage signaling at telomeres
title_full_unstemmed Fungal Ku prevents permanent cell cycle arrest by suppressing DNA damage signaling at telomeres
title_short Fungal Ku prevents permanent cell cycle arrest by suppressing DNA damage signaling at telomeres
title_sort fungal ku prevents permanent cell cycle arrest by suppressing dna damage signaling at telomeres
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4344518/
https://www.ncbi.nlm.nih.gov/pubmed/25653166
http://dx.doi.org/10.1093/nar/gkv082
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