Sebesta, Marek and Burkovics, Péter and Juhász, Szilvia and Zhang, Sufang and Szabó, Judit E. and Haracska, Lajos (2013) Role of PCNA and TLS polymerases in D-loop extension during homologous recombination in humans. DNA REPAIR, 12 (9). pp. 691-698. ISSN 1568-7864
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Abstract
Homologous recombination (HR) is essential for maintaining genomic integrity, which is challenged by a wide variety of potentially lethal DNA lesions. Regardless of the damage type, recombination is known to proceed by RAD51-mediated D-loop formation, followed by DNA repair synthesis. Nevertheless, the participating polymerases and extension mechanism are not well characterized. Here, we present a reconstitution of this step using purified human proteins. In addition to Pol delta, TLS polymerases, including Pol eta and Pol kappa, also can extend D-loops. In vivo characterization reveals that Pol eta and Pol kappa are involved in redundant pathways for HR. In addition, the presence of PCNA on the D-loop regulates the length of the extension tracks by recruiting various polymerases and might present a regulatory point for the various recombination outcomes. (c) 2013 The Authors. Published by Elsevier B.V. All rights reserved.
Item Type: | Article |
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Uncontrolled Keywords: | SPARTAN/C1ORF124; PROTEINS; ETA; DAMAGE; POL-KAPPA; SACCHAROMYCES-CEREVISIAE; REPLICATION STRESS; GENE CONVERSION TRACTS; TRANSLESION DNA-SYNTHESIS; STRAND-BREAK REPAIR; RECONSTITUTION; D-loop; DNA repair synthesis; Homologous recombination; TLS polymerases |
Subjects: | Q Science / természettudomány > QH Natural history / természetrajz > QH301 Biology / biológia Q Science / természettudomány > QH Natural history / természetrajz > QH301 Biology / biológia > QH3015 Molecular biology / molekuláris biológia |
SWORD Depositor: | MTMT SWORD |
Depositing User: | MTMT SWORD |
Date Deposited: | 26 Nov 2013 10:19 |
Last Modified: | 26 Nov 2013 10:19 |
URI: | http://real.mtak.hu/id/eprint/7481 |
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