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Quantitative Insights into Age-Associated DNA-Repair Inefficiency in Single Cells

Although double-strand break (DSB) repair is essential for a cell’s survival, little is known about how DSB repair mechanisms are affected by age. Here we characterize the impact of cellular aging on the efficiency of single-strand annealing (SSA), a DSB repair mechanism. We measure SSA repair effic...

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Detalles Bibliográficos
Autores principales: Young, Thomas Z., Liu, Ping, Urbonaite, Guste, Acar, Murat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744837/
https://www.ncbi.nlm.nih.gov/pubmed/31433994
http://dx.doi.org/10.1016/j.celrep.2019.07.082
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author Young, Thomas Z.
Liu, Ping
Urbonaite, Guste
Acar, Murat
author_facet Young, Thomas Z.
Liu, Ping
Urbonaite, Guste
Acar, Murat
author_sort Young, Thomas Z.
collection PubMed
description Although double-strand break (DSB) repair is essential for a cell’s survival, little is known about how DSB repair mechanisms are affected by age. Here we characterize the impact of cellular aging on the efficiency of single-strand annealing (SSA), a DSB repair mechanism. We measure SSA repair efficiency in young and old yeast cells and report a 23.4% decline in repair efficiency. This decline is not due to increased use of non-homologous end joining. Instead, we identify increased G1 phase duration in old cells as a factor responsible for the decreased SSA repair efficiency. Expression of 3xCLN2 leads to higher SSA repair efficiency in old cells compared with expression of 1xCLN2, confirming the involvement of cell-cycle regulation in age-associated repair inefficiency. Examining how SSA repair efficiency is affected by sequence heterology, we find that heteroduplex rejection remains high in old cells. Our work provides insights into the links between single-cell aging and DSB repair efficiency.
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spelling pubmed-67448372019-09-14 Quantitative Insights into Age-Associated DNA-Repair Inefficiency in Single Cells Young, Thomas Z. Liu, Ping Urbonaite, Guste Acar, Murat Cell Rep Article Although double-strand break (DSB) repair is essential for a cell’s survival, little is known about how DSB repair mechanisms are affected by age. Here we characterize the impact of cellular aging on the efficiency of single-strand annealing (SSA), a DSB repair mechanism. We measure SSA repair efficiency in young and old yeast cells and report a 23.4% decline in repair efficiency. This decline is not due to increased use of non-homologous end joining. Instead, we identify increased G1 phase duration in old cells as a factor responsible for the decreased SSA repair efficiency. Expression of 3xCLN2 leads to higher SSA repair efficiency in old cells compared with expression of 1xCLN2, confirming the involvement of cell-cycle regulation in age-associated repair inefficiency. Examining how SSA repair efficiency is affected by sequence heterology, we find that heteroduplex rejection remains high in old cells. Our work provides insights into the links between single-cell aging and DSB repair efficiency. 2019-08-20 /pmc/articles/PMC6744837/ /pubmed/31433994 http://dx.doi.org/10.1016/j.celrep.2019.07.082 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Young, Thomas Z.
Liu, Ping
Urbonaite, Guste
Acar, Murat
Quantitative Insights into Age-Associated DNA-Repair Inefficiency in Single Cells
title Quantitative Insights into Age-Associated DNA-Repair Inefficiency in Single Cells
title_full Quantitative Insights into Age-Associated DNA-Repair Inefficiency in Single Cells
title_fullStr Quantitative Insights into Age-Associated DNA-Repair Inefficiency in Single Cells
title_full_unstemmed Quantitative Insights into Age-Associated DNA-Repair Inefficiency in Single Cells
title_short Quantitative Insights into Age-Associated DNA-Repair Inefficiency in Single Cells
title_sort quantitative insights into age-associated dna-repair inefficiency in single cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744837/
https://www.ncbi.nlm.nih.gov/pubmed/31433994
http://dx.doi.org/10.1016/j.celrep.2019.07.082
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