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PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks
Poly adenosine diphosphate (ADP)–ribosylation (PARylation) by poly ADP-ribose (PAR) polymerases (PARPs) is an early response to DNA double-strand breaks (DSBs). In this paper, we exploit Dictyostelium discoideum to uncover a novel role for PARylation in regulating nonhomologous end joining (NHEJ). P...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153639/ https://www.ncbi.nlm.nih.gov/pubmed/21807880 http://dx.doi.org/10.1083/jcb.201012132 |
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author | Couto, C. Anne-Marie Wang, Hong-Yu Green, Joanna C.A. Kiely, Rhian Siddaway, Robert Borer, Christine Pears, Catherine J. Lakin, Nicholas D. |
author_facet | Couto, C. Anne-Marie Wang, Hong-Yu Green, Joanna C.A. Kiely, Rhian Siddaway, Robert Borer, Christine Pears, Catherine J. Lakin, Nicholas D. |
author_sort | Couto, C. Anne-Marie |
collection | PubMed |
description | Poly adenosine diphosphate (ADP)–ribosylation (PARylation) by poly ADP-ribose (PAR) polymerases (PARPs) is an early response to DNA double-strand breaks (DSBs). In this paper, we exploit Dictyostelium discoideum to uncover a novel role for PARylation in regulating nonhomologous end joining (NHEJ). PARylation occurred at single-strand breaks, and two PARPs, Adprt1b and Adprt2, were required for resistance to this kind of DNA damage. In contrast, although Adprt1b was dispensable for PARylation at DSBs, Adprt1a and, to a lesser extent, Adprt2 were required for this event. Disruption of adprt2 had a subtle impact on the ability of cells to perform NHEJ. However, disruption of adprt1a decreased the ability of cells to perform end joining with a concomitant increase in homologous recombination. PAR-dependent regulation of NHEJ was achieved through promoting recruitment and/or retention of Ku at DSBs. Furthermore, a PAR interaction motif in Ku70 was required for this regulation and efficient NHEJ. These data illustrate that PARylation at DSBs promotes NHEJ through recruitment or retention of repair factors at sites of DNA damage. |
format | Online Article Text |
id | pubmed-3153639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31536392012-02-08 PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks Couto, C. Anne-Marie Wang, Hong-Yu Green, Joanna C.A. Kiely, Rhian Siddaway, Robert Borer, Christine Pears, Catherine J. Lakin, Nicholas D. J Cell Biol Research Articles Poly adenosine diphosphate (ADP)–ribosylation (PARylation) by poly ADP-ribose (PAR) polymerases (PARPs) is an early response to DNA double-strand breaks (DSBs). In this paper, we exploit Dictyostelium discoideum to uncover a novel role for PARylation in regulating nonhomologous end joining (NHEJ). PARylation occurred at single-strand breaks, and two PARPs, Adprt1b and Adprt2, were required for resistance to this kind of DNA damage. In contrast, although Adprt1b was dispensable for PARylation at DSBs, Adprt1a and, to a lesser extent, Adprt2 were required for this event. Disruption of adprt2 had a subtle impact on the ability of cells to perform NHEJ. However, disruption of adprt1a decreased the ability of cells to perform end joining with a concomitant increase in homologous recombination. PAR-dependent regulation of NHEJ was achieved through promoting recruitment and/or retention of Ku at DSBs. Furthermore, a PAR interaction motif in Ku70 was required for this regulation and efficient NHEJ. These data illustrate that PARylation at DSBs promotes NHEJ through recruitment or retention of repair factors at sites of DNA damage. The Rockefeller University Press 2011-08-08 /pmc/articles/PMC3153639/ /pubmed/21807880 http://dx.doi.org/10.1083/jcb.201012132 Text en © 2011 Couto et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Couto, C. Anne-Marie Wang, Hong-Yu Green, Joanna C.A. Kiely, Rhian Siddaway, Robert Borer, Christine Pears, Catherine J. Lakin, Nicholas D. PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks |
title | PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks |
title_full | PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks |
title_fullStr | PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks |
title_full_unstemmed | PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks |
title_short | PARP regulates nonhomologous end joining through retention of Ku at double-strand breaks |
title_sort | parp regulates nonhomologous end joining through retention of ku at double-strand breaks |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153639/ https://www.ncbi.nlm.nih.gov/pubmed/21807880 http://dx.doi.org/10.1083/jcb.201012132 |
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