Research Paper
A requirement for polymerized actin in DNA double-strand break repair
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Volume 3, Issue 4 July/August 2012
Pages 384 - 395
http://dx.doi.org/10.4161/nucl.21055
Keywords: DNA damage, DSB repair, Ku70, Ku80, nuclear actin, polymeric actin
Authors: Christi Andrin, Darin McDonald, Kathleen M. Attwood, Amélie Rodrigue, Sunita Ghosh, Razmik Mirzayans, Jean-Yves Masson, Graham Dellaire and Michael J. Hendzel
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- Christi Andrin
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Department of Oncology; University of Alberta; Edmonton, AB Canada
- Darin McDonald
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Experimental Oncology; Cross Cancer Institute; Alberta Cancer Board; Edmonton, AB Canada
- Kathleen M. Attwood
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Departments of Pathology and Biochemistry and Molecular Biology; Dalhousie University; Halifax, NS Canada
- Amélie Rodrigue
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Genome Stability Laboratory; Laval University Cancer Research Center; Québec, QC Canada
- Sunita Ghosh
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Experimental Oncology; Cross Cancer Institute; Alberta Cancer Board; Edmonton, AB Canada
- Razmik Mirzayans
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Experimental Oncology; Cross Cancer Institute; Alberta Cancer Board; Edmonton, AB Canada
- Jean-Yves Masson
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Genome Stability Laboratory; Laval University Cancer Research Center; Québec, QC Canada
- Graham Dellaire
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Departments of Pathology and Biochemistry and Molecular Biology; Dalhousie University; Halifax, NS Canada; Beatrice Hunter Cancer Research Institute; Halifax, NS Canada
- Michael J. Hendzel
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Corresponding author: michaelh@cancerboard.ab.ca
Department of Oncology; University of Alberta; Edmonton, AB Canada; Experimental Oncology; Cross Cancer Institute; Alberta Cancer Board; Edmonton, AB Canada
Abstract:
Nuclear actin is involved in several nuclear processes from chromatin remodeling to transcription. Here we examined the requirement for actin polymerization in DNA double-strand break repair. Double-strand breaks are considered the most dangerous type of DNA lesion. Double-strand break repair consists of a complex set of events that are tightly regulated. Failure at any step can have catastrophic consequences such as genomic instability, oncogenesis or cell death. Many proteins involved in this repair process have been identified and their roles characterized. We discovered that some DNA double-strand break repair factors are capable of associating with polymeric actin in vitro and specifically, that purified Ku70/80 interacts with polymerized actin under these conditions. We find that the disruption of polymeric actin inhibits DNA double strand break repair both in vitro and in vivo. Introduction of nuclear targeted mutant actin that cannot polymerize, or the depolymerization of endogenous actin filaments by the addition of cytochalasin D, alters the retention of Ku80 at sites of DNA damage in live cells. Our results suggest that polymeric actin is required for proper DNA double-strand break repair and may function through the stabilization of the Ku heterodimer at the DNA damage site.
Received: March 6, 2012; Accepted: June 8, 2012; Published Online: June 12, 2012
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