Affiliation:
1. School of Molecular Cell Biology and Biotechnology, Tel Aviv University, Ramat Aviv, Israel
Abstract
PCNA, the ring that encircles DNA maintaining the processivity of DNA polymerases, is modified by ubiquitin and SUMO. Whereas ubiquitin is required for bypassing lesions through the DNA damage tolerance (DDT) pathways, we show here that SUMOylation represses another pathway, salvage recombination. The Srs2 helicase is recruited to SUMOylated PCNA and prevents the salvage pathway from acting. The pathway can be induced by overexpressing the PCNA unloader Elg1, or the homologous recombination protein Rad52. Our results underscore the role of PCNA modifications in controlling the various bypass and DNA repair mechanisms.
Funder
Israel Science Foundation
Israel Cancer Research Fund
Minerva Foundation
Publisher
American Society for Microbiology
Cited by
14 articles.
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